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The study examines the impact of the incorporation of quantum-sized nickel (Ni) nanoparticles in TiO2 (titanium dioxide) matrix at 1%, 3%, and 5% weight percentages by straightforward, easy, and potentially effective synthesis strategy of direct doping. The structural, morphological, optical, and electrical characterization studies of synthesized films are systematically done and the photovoltaic, photocatalytic applications are evaluated. The integration of nickel into TiO2 influences its photovoltaic properties by enhancing the open-circuit voltage (Voc). However, higher concentrations lead to increased recombination and defects, decreasing efficiency. On conducting photocatalytic studies, TiO2 doped with 1 wt. % nickel exhibits superior photocatalytic efficiency, surpassing that of undoped TiO2. This improvement in photovoltaic and photocatalytic performance is attributed to better charge separation and reduced recombination. However, optimizing nickel levels is crucial for maximizing benefits for the applications using the performed synthesis strategy. [ABSTRACT FROM AUTHOR]

We theoretically analyze the electronic transport properties of a monolayer graphene/insulator/superconductor (G I S) tunnel junction subject to a temperature gradient. For intrinsic graphene, the system shows always dissipative charge transport even in the presence of an electronic temperature difference between the two leads. Differently, the G I S produces a thermoelectric response when the graphene electrochemical potential is lifted to energies comparable to the zero-temperature gap of the superconductor, i.e., the system is particle–hole asymmetric. Indeed, the thermally biased G I S system is able to produce both a short-circuit Peltier current and an open-circuit Seebeck voltage. This thermoelectric effect is made of a linear conventional component, due to the intrinsic particle–hole asymmetry of the system, and a non-linear contribution, due to a further spontaneous particle–hole symmetry breaking. In most of the thermal and charge configurations of the G I S system, the linear component prevails. Concluding, the G I S system could be employed in the design of thermometers, electromagnetic radiation sensors, and heat engines with profound influence in superconducting quantum technologies. [ABSTRACT FROM AUTHOR]

The large Stokes shifts usually result in open circuit voltage (VOC) reduction, which will affect the photovoltaic performance of the material. Recently, three-dimensional organosulfide-halide perovskites (CYS)PbCl2 and (CYS)PbBr2 [CYS: +NH3(CH2)2S−] have received much attention in the photovoltaic field due to their higher stability and similar photoelectric properties (desirable direct bandgap, band dispersion, and light absorption) than MAPbX3 (X = Cl, Br, and I). Unfortunately, both materials exhibit large Stokes shifts emission. Thus, to be clear about their application prospects in the photovoltaic field, the origin of the large Stoke shift needs to be investigated. Moreover, the bandgaps of (CYS)PbBr2 (2.17 eV) and (CYS)PbCl2 (2.32 eV) are higher than the ideal bandgap value of (0.9–1.6 eV) for photovoltaic materials. Based on density functional theory, this paper explores the cause of large Stokes shifts and further improves the photovoltaic performance of the materials by halogen substitution. The calculation results show that the large Stokes shifts come from defect emission rather than intrinsic self-trapping emission and the I atom substitution can reduce the bandgap [(CYS)PbI2; gap = 1.85 eV] and enhance the optical absorption and carrier migration ability without destroying the direct bandgap. Our research will promote the experimental synthesis of more excellent perovskite photovoltaic materials. [ABSTRACT FROM AUTHOR]

Shunt resistance R sh is a critical parameter for photovoltaic cells designed for low light indoor applications because it negatively affects the open circuit voltage, fill factor, and conversion efficiency. Standard CIGS cells are known to have low R sh and are, therefore, unpromising candidates for indoor energy sources. In this paper, we extend the original work of Virtuani et al. by determining the electrical specifications of many CIGS cells with copper contents [Cu]/([Ga]+[In]) as low as 0.33 and gallium contents between 0.28 and 0.81. First, IV data are fitted by a standard single-diode electrical circuit model for each illumination, resulting in light-dependent parameters. Then, we use a procedure based on a single dataset of electrical variables, i.e., independent of light, corrected by the experimental collection function, which captures light-dependent physical mechanisms. In this way, we are able to correctly reproduce the illuminance dependence of the electrical response of the PV cell over three orders of magnitude, in particular with a fixed value of the shunt resistance. The highest R sh is obtained with a low copper composition of 0.5 , regardless of the gallium composition. [ABSTRACT FROM AUTHOR]

Ultra-thin solar cells display high intrinsic radiation tolerance, making them interesting for space applications. This study investigates the dependence of the open-circuit voltage degradation and overall current–voltage behavior of devices with 80 nm thick GaAs absorber layers, on their absorber layer doping concentration and the radiation type used to introduce damage. The radiation types used were 1 MeV electrons and 20 keV, 100 keV, and 1 MeV protons. It is shown that the open-circuit voltage degradation rate increases with absorber layer doping concentration. This is linked to the increase in trap-assisted tunneling enhancement of the recombination rate, facilitated by the increase in electric field strength in the absorber layer with doping concentration. Trap-assisted tunneling is also found to contribute to the high local ideality factors observed in these devices, exceeding values of 2, and to be responsible for the trend of an increasing ideality factor with doping concentration. The significant role of trap-assisted tunneling in the devices is established through fitting of dark current–voltage data using a custom recombination–generation model. An open-circuit voltage degradation rate and local ideality factor curves are also shown to vary with radiation type, despite accounting for their differences in non-ionizing energy loss. This is corroborated by corresponding trends in carrier lifetime damage constants, extracted from the fitting of the dark current–voltage curves. This suggests that the introduction or behavior of radiation damage differs between ultra-thin and conventional, thicker solar cells, where non-ionizing energy loss theory tends to be reliable, especially over the studied proton energy range. [ABSTRACT FROM AUTHOR]

A large open-circuit voltage (VOC) deficit is the major challenge hindering the efficiency improvement of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. Cation substitution, or doping, is usually an effective strategy to achieve carrier regulation and improve efficiency. In this work, we developed a rare-earth element lanthanum (La) doped CZTSSe thin-film solar cell by directly introducing La3+ ions into the CZTS precursor solution. Such a proposed La doping approach could effectively enhance light harvesting, adjust the bandgap, and increase the electron diffusion length. Furthermore, appropriate concentrations of La doping can reduce harmful defect cluster. Benefiting from the La doping, the VOC significantly increases from 431 to 497 mV. Consequently, the power conversion efficiency is enhanced significantly from 6.54% (VOC = 431 mV, JSC = 25.50 mA/cm2, FF = 58.28%) for the reference cell to 10.21% (VOC = 497 mV, JSC = 35.20 mA/cm2, FF = 58.41%) for the optimized La-doped cell. This research provides a new direction for enhancing the performance of CZTSSe cells, offering promising prospects for the future of CZTSSe thin-film solar cells. [ABSTRACT FROM AUTHOR]

An analytical device physics model is presented for determining the energy conversion efficiency of semiconductor nanowire array-based radial (core–shell) p-i-n junction betavoltaic cells for two- and three-dimensional radioisotope source geometries. Optimum short-circuit current density J sc , open-circuit voltage V oc , fill factor F F , and energy conversion efficiency η are determined for various nanowire properties, including dopant concentration, nanowire length, core diameter, and shell thickness, for Si, GaAs, and GaP material systems. A maximum efficiency of 8.05 % was obtained for GaP nanowires with diameter 200 nm (p-core diameter, i-shell, and n-shell thicknesses of 24, 29.4, and 58.6 nm, respectively), length 10 μ m , acceptor and donor concentrations of 10 19 and 5 × 10 18 cm − 3 , respectively, and a 3D source geometry. [ABSTRACT FROM AUTHOR]

Ag-doping treatment is a popular method for enhancing the performance of kesterite-structured Cu2ZnSn(S,Se)4 (CZTSSe) solar cells. Among the various methods, incorporating a high concentration of Ag+ into an absorber surface has proven to be particularly effective. However, the exact mechanisms behind this improvement are still unclear. This study aims to investigate the key factors that improve device performance through simulation. Specifically, the influence of the change in the carrier density, CuZn antisite defects, interface defect density, and formation of an n-type AZTSSe surface after heavy surface Ag doping have been examined. The simulation results indicate that the formation of an n-type AZTSSe layer on an absorber surface can significantly improve the open circuit voltage (VOC) and overcome the efficiency saturation problem induced by severe interface recombination for CZTSSe devices with a negative conduction band offset (CBO), compared to other affecting factors. This is because the modified conduction band alignment and the realization of interface-type inversion reduce interface recombination and retard the Fermi level pinning. However, the formation of interface-type inversion does not significantly improve CZTSSe devices with a positive CBO, as these devices already have weaker interface recombination. This work implies that the formation of an n-type AZTSSe layer is crucial for further improving the performance of CZTSSe devices with a negative CBO and can pave the way for improving the performance of thin film solar cells with severe interface recombination. [ABSTRACT FROM AUTHOR]

All-inorganic CsPbI2Br inverted perovskite solar cells (PSCs) have drawn increasing attention because of their outstanding thermal stability and compatible process with tandem cells. However, relatively low open circuit voltage (Voc) has lagged their progress far behind theoretical limits. Herein, we introduce phenylmethylammonium iodide and 4-trifluoromethyl phenylmethylammonium iodide (CFPMAI) on the surface of a CsPbI2Br perovskite film and investigate their passivation effects. It is found that CFPMAI with a –CF3 substituent significantly decreases the trap density of the perovskite film by forming interactions with the under-coordinated Pb2+ ions and effectively suppresses the non-radiative recombination in the resulting PSC. In addition, CFPMAI surface passivation facilitates the optimization of energy-level alignment at the CsPbI2Br perovskite/[6,6]-phenyl C61 butyric acid methyl ester interface, resulting in improved charge extraction from the perovskite to the charge transport layer. Consequently, the optimized inverted CsPbI2Br device exhibits a markedly improved champion efficiency of 14.43% with a Voc of 1.12 V, a Jsc of 16.31 mA/cm2, and a fill factor of 79.02%, compared to the 10.92% (Voc of 0.95 V) efficiency of the control device. This study confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement. [ABSTRACT FROM AUTHOR]

In this study, the degradation behavior of flexible GaInP/GaAs/InGaAs (IMM3J) solar cells and their metamorphic subcells under 1 MeV electron irradiation was investigated. The remaining factors such as short-circuit current density (Jsc), open-circuit voltage (Voc), and maximum power (Pmax) were 95.62, 85.52, and 79.73%, respectively, at an irradiation fluence of 2 × 1015 e/cm2. The spectral responses of the InGaAs and GaAs subcells degraded significantly, and the InGaAs subcell experienced greater degradation than the GaAs subcell after irradiation. In addition, the current-limiting unit was switched from GaInP to InGaAs after irradiation. Defect analysis by deep-level transient spectroscopy (DLTS) revealed that with increasing irradiation fluence, the defects that had the greatest impact on the performance of GaAs subcells were EV + 0.36 and EV + 0.42 eV. For InGaAs subcells, the defects that had the greatest impact on the performance were EV + 0.29 and EV + 0.24 eV. The decrease in the minority carrier lifetime is the main reason for the decrease in the electrical performance of solar cells, and the variation in the effective minority carrier lifetime (τeff) in the subcells with the irradiation fluence was calculated based on the DLTS results. At a fluence of 2 × 1015 e/cm2, the τeff of the GaAs and InGaAs subcells decreased from 2.93 × 10−10 and 9.10 × 10−10 s to 1.56 × 10−11 and 1.60 × 10−12 s, respectively. These results provide a reference for predicting the degradation of short-circuit current and open-circuit voltage of flexible IMM3J. [ABSTRACT FROM AUTHOR]

The ability to spatially resolve the carrier mobility profile along the cross section of micrometer-thin solar cells is vital, both for fundamental studies in photovoltaics and as quality control for reproducibly obtaining high conversion efficiencies in commercial solar cell modules. Presently, no technique capable of such an endeavor is available to the best of our knowledge. Here, we introduce a novel method capable of profiling the carrier mobility along the z axis in thin-film photovoltaics. Our setup is based on the integration of photogenerated charge extraction by linearly increasing voltage (p-CELIV) with a scanning confocal optical microscope (SCOM) toward a confocal and cross-sectional p-CELIV (cs-p-CELIV) system. As monomolecular recombination of excess carriers is the most frequent radiative pathway for electrons and holes in solar cells at low power density of illumination, while multimolecular recombination dominates at high power, enhanced multimolecular recombination occurs at the SCOM focal plane. Thus, the cs-p-CELIV signal provides enhanced information on the mobility of all of the cross-sectional layers except the focal plane. By scanning the focal plane along the z axis, the mobility profile can be derived. To demonstrate our technique, we use it to investigate the carrier mobility in three hydrogenated amorphous silicon (a-Si:H) solar cells. The mobility profiles obtained by cs-p-CELIV correlate well with well-known depletion layer effects and the H content profile in a-Si:H, which is measured independently. Our findings are in excellent agreement with models suggesting a critical role of Si–H bonding in locally determining the carrier mobility in a-Si:H. [ABSTRACT FROM AUTHOR]

Thermodynamics shows that the open-circuit voltage (V o c) of a solar cell is dependent on the external radiative efficiency at V o c . In planar solar cells with low photon recycling probability, this efficiency is limited to 2% due to total internal reflection of the emitted light, providing a penalty of 101 mV to the V o c . Tapered nanowire solar cells allow for an adiabatic expansion of the guided optical mode into air, allowing to reduce this loss. For this purpose, we first perform simulations of the photon escape probability in tapered nanowires with both finite difference time domain simulations as well as with rigorous coupled-wave analysis, showing photon escape probabilities up to 47.2% for normally tapered nanowires and up to 92% for inversely tapered nanowires. We subsequently show that by fine tuning the recipe for reactive ion etching of the tapered InP nanowires, we can decrease the nanowire tapering angle from 4.5° down to 1.8°, allowing to significantly increase the measured external radiative efficiency. We finally observe an open-circuit voltage of 0.746 V at a tapering angle of 2.46°. [ABSTRACT FROM AUTHOR]

We investigate microlenses that selectively focus the light on only a small fraction of all nanowires within an arrayed InP nanowire solar cell. The nano-concentration improves both the short-circuit current (J s c ) and the open-circuit voltage (V o c ) of the solar cell. For this purpose, polymethyl methacrylate microlenses with 6 μm diameter were randomly positioned on top of an arrayed nanowire solar cell with 500 nm pitch. The microlenses were fabricated by first patterning cylindrical micropillars, which were subsequently shaped as lenses by using a thermal reflow process. The quality of the microlenses was experimentally assessed by Fourier microscopy showing strong collimation of the emitted photoluminescence. By analyzing the slope of the integrated photoluminescence vs excitation density, we deduce a substantial enhancement of the external radiative efficiency of a nanowire array by adding microlenses. The enhanced radiative efficiency of the lensed nanowire array results in a clear enhancement of the open-circuit voltage for a subset of our solar cells. The microlenses finally also allow to increase the short-circuit current of our relatively short nanowires, providing a route to significantly reduce the amount of expensive semiconductor material. [ABSTRACT FROM AUTHOR]

Global energy shortage puts stringent demand for energy harvesters capable of transforming external green vibration sources into electrical power. Employing a self-biased magnetoelectric (ME) composite of FeCuNbSiB/Ni/PZT (lead zirconate titanate), a prototype of vibration energy harvester is designed and fabricated. The energy harvester has a circular orbit in which a permanent magnetic cylinder reciprocates once an initial kinetic energy is provided. Upon a vibration signal, like handshaking, movement of the permanent magnetic cylinder causes an alternative magnetic field, which was applied on the ME composite. Via magnetic-force-electrical coupling, the ME composite of FeCuNbSiB/Ni/PZT produces output voltage. Finite element simulation is carried out to reveal the underlying mechanism of the harvester. The analysis shows that a maximum output voltage of 7.63 V can be obtained once an original potential energy is applied for the magnet. In particular, the magnet moves back and forth automatically inside the circular orbit with no need to further apply the energy. The effectiveness of the energy output is experimentally verified. When handshaking the energy harvester, a maximum open-circuit voltage of 5.51 V can be generated. The study offers a solution for power supplying some miniaturized or portable devices, such as small hand set and pedometer. [ABSTRACT FROM AUTHOR]

Realizing the graded bandgap in absorber layer is very essential for high efficient thin film solar cells. However, such bandgap modification in kesterite-structured Cu2ZnSnSe4 is normally realized via high temperature sulfurization process (above 500°C), which is not only difficult to control the sulfurization depth, but also introduces additional deep defects because of the decomposition of absorber layer at such high temperature. In this study, a low-temperature sulfurization process (150°C) is developed. Such process not only inhibits the decomposition of Cu2ZnSnSe4 films and controls the elemental distribution very well, but also increase the surface bandgap of the absorber layer and form a gradient energy bandgap. Also, the density of deep-level defects in the Cu2ZnSnSe4 layer is reduced. As a consequence, the open circuit voltage of the solar cell is improved by 60 mV. This study paves the way towards the high efficient kesterite solar cell and other solar cells. [ABSTRACT FROM AUTHOR]

Realizing the graded bandgap in absorber layer is very essential for high efficient thin film solar cells. However, such bandgap modification in kesterite-structured Cu2ZnSnSe4 is normally realized via high temperature sulfurization process (above 500°C), which is not only difficult to control the sulfurization depth, but also introduces additional deep defects because of the decomposition of absorber layer at such high temperature. In this study, a low-temperature sulfurization process (150°C) is developed. Such process not only inhibits the decomposition of Cu2ZnSnSe4 films and controls the elemental distribution very well, but also increase the surface bandgap of the absorber layer and form a gradient energy bandgap. Also, the density of deep-level defects in the Cu2ZnSnSe4 layer is reduced. As a consequence, the open circuit voltage of the solar cell is improved by 60 mV. This study paves the way towards the high efficient kesterite solar cell and other solar cells. [ABSTRACT FROM AUTHOR]

Here, we describe a fully in situ method of fabricating light-scattering structures on III-V materials that generates a rough morphology via vapor phase etching and redeposition. Fully in situ methods support higher industrial throughput by utilizing the growth reactor to generate the light-trapping structures after device growth without removal from the reactor. We use HCl and PH3 to etch and redeposit scattering morphologies on Ga0.5In0.5P in a dynamic hydride vapor phase epitaxy (D-HVPE) reactor. We show that the addition of PH3 leads to redeposition during the vapor phase HCl etching of Ga0.5In0.5P and that HCl flow rate and time exposed to HCl-PH3 each independently cause a linear increase in the redeposited feature size, indicating that redeposition proceeds by island growth in a III-Cl-limited, hydride-enhanced HVPE regime. Auger electron spectroscopy and scanning transmission electron microscopy with energy dispersive spectroscopy (STEM-EDS) reveal redeposition to be highly Ga-rich GaInP, i.e., Ga(In)P. The Ga-rich nature of the redeposition results from the higher thermodynamic driving force for Ga incorporation than for In during HVPE growth and the difference in the volatility of the III-Cl etch products. The resulting morphologies have high broadband scattering, as determined by normal specular reflectance and integrating sphere measurements, indicating effectiveness as light-scattering structures. In a 270-nm-thick GaAs photovoltaic device with a textured back surface, we achieve a 4.9% increase in short circuit current density (JSC) without any loss in open-circuit voltage (VOC) relative to a planar control using only a 60 s in situ texturing treatment. [ABSTRACT FROM AUTHOR]

Although two-dimensional (2D) transition metal oxide monolayers have shown potential for applications in metal-ion batteries, the heterostructures of this family are yet to be studied in details for energy storage applications. In this work, we have made the heterostructure by taking half-metallic ferromagnetic 2D transition metal oxide CoO 2 and semiconducting MnO 2 monolayers and demonstrated its potential application as a cathode material in lithium and sodium-ion batteries by performing first-principles calculations using density functional theory approach. We have systematically studied the electronic structure and stability of the MnO 2 / CoO 2 heterostructure. We have carefully examined the adsorption and diffusion behavior of metal ions (lithium and sodium). Our structure has offered a maximum adsorption energy of − 3.84 eV, which is greater than the adsorption energy of individual monolayers. We found that the lowest diffusion barrier is 0.4 eV for lithium ion and 0.32 eV for sodium ion. Also, our system has shown a maximum open circuit voltage of 2.18 V for lithium ion battery and 0.32 V for Na-ion battery. The specific capacity is found to be 584 mAh g − 1 for lithium ion and 529 mAh g − 1 for sodium ion battery. These findings can serve as a proof that the MnO 2 / CoO 2 heterostructure should be considered as a potential cathode for lithium- and sodium-ion batteries. [ABSTRACT FROM AUTHOR]

We report on the application of solution-based p-type electrical doping using 12-molybdophosphoric acid hydrate (PMA) to the fabrication of organic tandem solar cells. Such a doping approach leads to a spatially confined vertical doping profile down to a limited depth from the surface of polymer films, thus allowing the hole-collecting component of the charge recombination stack to be embedded in the photoactive layer of the bottom sub-cell. This simplifies the device architecture by removing the need for an extra dedicated hole-collecting layer. It is shown that this novel charge recombination stack comprising a PMA-doped bottom photoactive layer and a trilayer of Ag/AZO/PEIE is compatible with a solution-processed top photoactive layer. The fabricated inverted organic tandem solar cells exhibit an open-circuit voltage that is close to the sum of the open-circuit voltages of the individual sub-cells, and a fill factor that is close to the better fill factor of the two sub-cells. [ABSTRACT FROM AUTHOR]

Covalent organic framework (COF) exhibits the great potential to promote proton conduction under low relative humidity for proton exchange membranes (PEMs). In this research, quick and stable proton conduction has been achieved since the prepared COF and polyvinylidene fluoride (PVDF) nanofibers are believed to constitute successive proton conduction channels. The PVDF-COF nanofibers membrane is prepared through the in-situ growth of COF along PVDF nanofibers. The fine compatibility can drive the stable combination of COF with the PVDF nanofibers in PVDF-COF nanofibers. Most importantly, the fibrous PVDF nanofibers accelerate proton conduction through confining the proton conduction pathways. Additionally, ionic liquids of 1-butyl-3-methylimidazolium chloride (BmimCl) and 1-butyl-3-methylimidazole hexafluorophosphate (BmimPF 6) as proton conduction carriers have been introduced to accelerate proton conduction in the prepared PVDF-COF/BmimCl/PA and PVDF-COF/BmimPF 6 /PA membranes. Phosphoric acid (PA) molecules are combined by COF and ionic liquid cations with the formation of intermolecular hydrogen bonds. As a result, the PVDF-COF/BmimPF 6 /PA membrane exhibits the proton conductivity of (1.81 ± 0.07) × 10−1 S/cm at 160 °C. The long-term proton conductivity stability is determined, deriving from the proton conductivities of 1.77×10−2 S/cm at 80 °C and 1.42×10−2 S/cm at 110 °C in the 400 h non-stop measurement. The single fuel cell equipped with the PVDF-COF/BmimPF 6 /PA membrane represents the open circuit voltage of 0.927 V and the peak power density of 178.8 mW/cm2 at 100 °C, 0.907 V and 326.5 mW/cm2 at 120 °C. [Display omitted] • Covalent organic framework is prepared. • COF and ionic liquid synergistically promote proton conduction. • Peak power densities are 178.8 mW/cm2 at 100 °C and 326.5 mW/cm2 at 120 °C. [ABSTRACT FROM AUTHOR]

Traditional studies on boride cermet have rarely considered the effects of the synergistic interactions among their multiple components on their microstructure and properties. In this study, FeCrNiCo-boride cermet is prepared for the first time via hot-press sintering. The microstructure evolution and corrosion resistance of the cermet are investigated for sintering temperatures in the range of 1000–1300 °C. The results show that the phase comprises Mo 2 FeB 2 , MoB 2 , and FCC phases (including that of FeCrNiCo or various intermetallic solid solutions formed by FeCrNiCo decomposition). Owing to its low Gibbs free energy, Mo 2 FeB 2 occurs in the hard phase. Cr atoms dissolve into the crystal lattice and stabilise the Mo 2 FeB 2 crystals. A certain amount of MoB 2 is also present in the hard phase. The bond phase is formed by alloying elements and solid solutions. The cermet sintered at 1100 °C exhibits the least structural defects, highest cermet content, and best corrosion resistance; the porosity is 9.94 % and phase ratio of cermet is 48.9 %. The cermet phase has the smallest grain size of 5.96 μm. The equilibrium potential (E corr) is −0.52 V, corrosion current density (I corr) is 2.07 × 10−6 A/cm2, and open-circuit potential (OCP) in a 3.5 % NaCl solution is −0.34 V. [ABSTRACT FROM AUTHOR]

In this study, a piezoelectric nanogenerator (PENG) based on multilayer composite fiber had good and stable piezoelectric output performance, which could realize biomechanical energy collection and human movement monitoring. The polyvinylidene fluoride‐hexafluoryl propylene (P(VDF‐HFP)) composite fiber doped with MXene was used as a promising piezoelectric functional layer (MPFP). By electrospinning, P(VDF‐HFP) composite fiber was constructed by alternating electrospinning with polyurethane (TPU) nanofibers layer by layer. The adoption of MXene as a functional filler promoted the transformation of P(VDF‐HFP) from α to piezoelectric β‐crystal, the piezoelectric β‐crystal content of P(VDF‐HFP) increased, and the dielectric properties and polarization levels were enhanced. At the same time, the multi‐layer structure design improved the piezoelectric sensitivity and mechanical properties of the composite fiber, and the composite fiber was more flexible and had longer tensile strain. With excellent dielectric and mechanical properties, 3MPFP/TPU/3MPFP/TPU multilayer composite fibers showed piezoelectric sensitivity of 10.88 V/kPa. Under the action of palm pressing, the PENG generated an open circuit voltage of 25 V, and the voltage signal of the device under different motion forms had specific characteristics such as peak value, frequency, and shape, which could be used to realize the analysis of human motion forms. This study provided an efficient, simple, and creative new idea for the application of flexible energy storage electronic devices, PENGs, and piezoelectric sensors. [ABSTRACT FROM AUTHOR]

In this study, Ge4+ was incorporated into the ceramic matrix of nickel-based anode materials, synthesizing anode materials NiO-Gd 0.1 Ce 0.9-x Ge x O 1.95 (x = 0.01, 0.04, 0.07) and NiO-Ce 0.9 Gd 0.1 O 2–δ. Corresponding anode support samples were also prepared, designated as A-C GDC , A-C 1Ge , A-C 4Ge , and A-C 7Ge. Additionally, single cell samples using the newly co-doped anode materials were prepared, identified as C-C GDC , C-C 1Ge , C-C 4Ge , and C-C 7Ge. The research indicates that after doping the ceramic phase framework with Ge4+, these composite anode materials exhibit the potential to withstand more redox cycles than C-CGDC without catastrophic mechanical structural damage or degradation in electrochemical performance. Particularly, after incorporating 7mol% Ge4+ into the ceramic backbone, the issue of 86 % strain accumulation in the anode support was mitigated. Additionally, the ion doping ratio is closely linked to the stability of the single cell samples, with the A-C 7Ge sample able to withstand up to 11 extreme recycling sessions at 700 °C without complete structural failure, improving structural stability by approximately 57 % compared to A-C 1Ge. In terms of electrochemical output performance, the impedance of C-C 1Ge prior to complete failure was nearly double that before oxidation-reduction, with a maximum power density reduction of about 26.47 %. As the co-doping concentration in the ceramic phase reached 7mol%, the impedance increase during single cell cycle testing was about four times smaller, with C-C 7Ge 's impedance before mechanical failure only 37 % higher than before cycling, and a reduction in maximum power density of just 11.11 %. Moreover, during consecutive cycling tests, the average damage to the open-circuit voltage was only 0.02V, showing almost no negative impact from the cycling operations, and it maintained efficient output performance after multiple cycles. Therefore, the newly synthesized nickel-based anode materials, modified via co-doping methods within the ceramic phase, can be considered as potential composite anode materials for intermediate-temperature solid oxide fuel cells. [ABSTRACT FROM AUTHOR]

For metal-supported solid oxide fuel cells (MS-SOFCs), gadolinium-doped ceria (GDC) is one of the most promising electrolyte materials due to its high ionic conductivity. The plasma spraying technique has unique advantages in the preparation of MS-SOFCs, such as high efficiency, low cost, and low thermal impact on the metal support. However, few studies have been conducted on the preparation of dense GDC electrolytes using plasma spraying technology. In addition, it is not clear whether the composition and Ce valence state of GDC change during the plasma spraying process. In order to investigate this issue, GDC electrolytes were fabricated by atmospheric plasma spraying (APS) and vacuum plasma spraying (VPS) techniques. It is found that the GDC electrolyte fabricated by VPS is denser and has better electrochemical performance. The open circuit voltage and maximum power density of the VPS-cell at 600 °C are 0.90 V and 175.7 mW/cm2, respectively, while those of the APS-cell are 0.86 V and 124.8 mW/cm2, respectively. Moreover, the valence state of Ce4+ in the GDC electrolyte remains unchanged after plasma spraying, while the composition of Ce/Gd changes. This work successfully fabricates GDC electrolytes with qualified performance and provides a reference for further optimizing spraying parameters to prepare high-performance MS-SOFC. [ABSTRACT FROM AUTHOR]

One SMEG can generate a maximum V oc and I sc of 0.57 V and 66 μA when a small amount of LiCl is dropped on one side at ambient humidity. V oc and I sc reach up to 3.55V and 204 μA when six SMEGs are connected in series or in parallel. The series connection of six SMEGs successfully lit an LED and a calculator, respectively. [Display omitted] In response to the energy crisis caused by the exhaustion of fossil energy sources, as well as to combat global warming and achieve carbon neutrality, a sandwiched-structure fabric-based moisture-enabled electricity generator (SMEG) has been developed. Cotton fabric coated with MWCNT and PEDOT: PSS solution is used as the upper and bottom electrodes, while the acid-treated cotton fabric with coating PVA and HCl hydrogel electrolyte serves as the middle layer. A single SMEG can generate a maximum open-circuit voltage (V oc) of 0.44 V and a maximum short-circuit current (I sc) of 30 μA. When a drop of LiCl is dripped on one side of SMEGs, the maximum V oc and I sc increases to 0.57 V and 66 μA, respectively. The decline in output performance slows down when LiCl is applied. The V oc increases almost linearly in series and reaches 3.55 V when six SMEGs are connected, while the I sc increases linearly in parallel and reaches 204 μA when six SMEGs are connected. The maximum power density of a single SMEG yields 0.29 μW/cm2 with an external resistance of 1 kΩ. The series connection of six SMEGs successfully lit an LED and a calculator under ambient humidity conditions, demonstrating their potential application in small electronics. [ABSTRACT FROM AUTHOR]

Highlights Three‐component piezoelectric composites, with castor‐oil‐derived polyurethane (COPU) as the matrix, reinforced with barium titanate (BTO) microparticles (as the primary piezo‐active inclusion) and with multiwalled carbon nanotubes (MWCNTs) were synthesized. BTO content is varied (3, 12, and 25 vol%), while the MWCNTs content is maintained constant at 0.65 wt% (0.37 vol%) w.r.t. the COPU matrix. The addition of MWCNTs significantly enhances the piezoelectric strain coefficient (d33$$ {d}_{33} $$), relative dielectric constant (k/k0), and piezoelectric response, that is, open circuit voltage (VOC) of the piezo‐composites. The (COPU/MWCNTs)/25 vol% BTO composite gives a d33$$ {d}_{33} $$ value of 1.8 ± 0.1 pC/N, an increase of ~1.38 times compared to COPU/25 vol% BTO composite (with a d33$$ {d}_{33} $$ value of 1.3 ± 0.1 pC/N). The relative dielectric constant (k/k0) value of two‐component COPU/BTO (25.0 vol%) increased from 10.34 ± 0.06 to 11.15 ± 0.05 by addition of 0.65 wt% MWCNTs. A maximum open circuit voltage of ~19.6 V for three‐component (COPU/MWCNTs)/ 25 vol% BTO composite was obtained at 45 N load and at 5 Hz frequency. This value (VOC) is ~1.29 times higher compared to COPU/25 vol% BTO composite (with VOC ~ 15.2 V). The k/k0 and d33$$ {d}_{33} $$ values and elastic moduli obtained via experiments were further compared with those obtained from finite element analyses based on kinematic uniform boundary conditions (KUBC) and from Eshelby–Mori–Tanaka micromechanics extended to the domain of linear piezoelectric composites. Castor‐oil‐derived (COPU/MWCNTs/BTO) three‐component composites were synthesized Integration of MWCNTs enhances d33$$ {d}_{33} $$ by ~1.38 times for COPU/25 vol% BTO Elastic modulus and electrical conductivity increased with the addition of MWCNTs Computational predicted k/k0 and d33$$ {d}_{33} $$ values closely match to experimental data [ABSTRACT FROM AUTHOR]

Summary: Solar‐powered devices, such as wireless networks, are a crucial component of the Internet of Things (IoT). Designing and creating a solar cell architecture with an extended light absorption regime at a reasonable cost is therefore exceedingly important. All inorganic bismuth‐based Cs2AgBiI6 planar perovskite solar cells (PSCs) have garnered enormous significance due to their exceptional stability against oxygen, heat, and moisture. However, the power conversion efficiencies of Cs2AgBiI6‐based planar PSCs remain relatively low, primarily due to their limited light absorption range and interfacial charge recombination losses. This issue can be effectively addressed using a novel multi‐absorber architecture that incorporates dual absorbers with both lower band gap and wider band gap materials. This approach extends the light absorption range, enabling maximal utilization of the solar spectrum. Therefore, this article incorporates numerical modeling and guided optimization of ITO/ETL/Cs2AgBiI6/Fa0.75Cs0.25SnI3/HTL/Ag dual absorber‐based heterojunction structure to improvise the power conversion efficiency of Cs2AgBiI6‐based single‐absorber PSCs. The proposed configuration employs dual perovskite absorber layers (PALs) consisting of wide band gap Cs2AgBiI6 (1.6 eV) as the top absorber layer along with narrow bandgap Fa0.75Cs0.25SnI3 (1.27 eV) to act as the bottom absorber layer. Before evaluating the bilayer configuration, two standalone PSC architectures, namely, ITO/ETL/Fa0.75Cs0.25SnI3/HTL/Ag (D1)‐ and ITO/ETL/Cs2AgBiI6/HTL/Ag (D2)‐based PSC have been simulated and computed to perfectly fit the earlier anticipated state of art results. After effective validation of the photovoltaic parameters of the standalone architectures, both the absorber layers are appraised to constitute a dual active layer configuration ITO/ETL/Cs2AgBiI6/Fa0.75Cs0.25SnI3/HTL/Ag (D3) maintaining the overall absorber layer width constant to elevate the overall solar cell efficiency. Herein, a combination of various competent hole transport layers (HTLs) such as CBTS, CFTS, Cu2O, CuI, CuO, CuSCN, P3HT, PEDOT:PSS, and Spiro‐OMeTAD, as well as electron transport layers (ETLs) like C60, CeO2, IgZo, PCBM, TiO2, WS2, and ZnO, are adopted and compared to attain highly efficient bilayer PSC configuration. The crucial variables of all ETL‐ and HTL‐based proposed bilayer solar cell configurations including the thickness of PALs, the width of the carrier transport layers, defect densities of transport layers, the effect of operating temperature, series, and shunt resistances have been extensively optimized and tuned to attain preeminent photovoltaic power conversion efficiencies (PCEs) and quantum efficiencies (QEs). It has been well evinced that the proposed configuration with dual‐absorber layers could effectively widen the light absorption regime to the near‐infrared range and thus significantly contribute toward enhanced photovoltaic performance. The simulation results attained with SCAPS showcase the outstanding performance of the proposed dual active layer solar structure obtained with the combination of CuSCN HTL and TiO2 ETL pair. The work concludes a 35.01% optimized efficient ITO/TiO2/Cs2AgBiI6(PAL‐2)/Fa0.75Cs0.25SnI3(PAL‐1)/CuSCN/Ag bilayer solar cell configuration with enhanced short circuit current density (Jsc) of 32.24 mA/cm2, open circuit voltage (Voc) of 1.273 V, and 85.31% fill factor (FF) with 0.6‐ and 0.8‐μm PAL‐1 and PAL‐2 width respectively and 1014‐cm−3 defect density under AM1.G solar spectrum illumination with 1000‐W/m2 light power density. The proposed eco‐friendly solar structure will also help in providing power backup to the next‐generation communication units and devices. Notably the dual‐absorber structure integrating Cs2AgBiI6 and Fa0.75Cs0.25SnI3 materials demonstrates significant advantages in quantum efficiency and spectral coverage compared to using either material independently as single absorbers. The proposed model achieves a peak efficiency of approximately 93% across a spectral range of 300–975 nm, surpassing the 90% efficiency obtained with a single Cs2AgBiI6 absorber covering 300–700 nm. Moreover, it exceeds the 89% efficiency achieved by the single Fa0.75Cs0.25SnI3 absorber within the 300‐ to 974.5‐nm spectral range. Solar cells play a pivotal role in ensuring the sustainability, reliability, and cost efficiency of powering wireless nodes, especially in remote or environmentally sensitive areas where traditional power sources may be inadequate or unavailable. The proposed PSC, with a PCE of 35.01%, can generate 350.1 watts under standard test conditions. This provides sufficient power to support approximately 70 wireless nodes, including wireless sensor nodes, IoT devices, and others, each consuming approximately 5 watts of power. [ABSTRACT FROM AUTHOR]

Two-step photon upconversion solar cells (TPU-SCs) based on III–V semiconductors can achieve enhanced sub-bandgap photon absorption because of intraband transitions at the heterointerface. From a technological aspect, the question arose whether similar intraband transitions can be realized by using perovskite/III–V semiconductor heterointerfaces. In this article, we demonstrate a TPU-SC based on a CsPbBr3/GaAs heterointerface. Such a solar cell can ideally achieve an energy conversion efficiency of 48.5% under 1-sun illumination. This is 2.1% higher than the theoretical efficiency of an Al0.3Ga0.7As/GaAs-based TPU-SC. Experimental results of the CsPbBr3/GaAs-based TPU-SC show that both the short-circuit current JSC and the open-circuit voltage VOC increase with additional illumination of sub-bandgap photons. We analyze the excitation power dependence of JSC for different excitation conditions to discuss the mechanisms behind the enhancement. In addition, the observed voltage-boost clarifies that the JSC enhancement is caused by an adiabatic optical process at the CsPbBr3/GaAs heterointerface, where sub-bandgap photons efficiently pump the electrons accumulated at the heterointerface to the conduction band of CsPbBr3. Besides the exceptional optoelectronic properties of CsPbBr3 and GaAs, the availability of a CsPbBr3/GaAs heterointerface for two-step photon upconversion paves the way for the development of high-efficiency perovskite/III–V semiconductor-based single-junction solar cells. [ABSTRACT FROM AUTHOR]

Sodium-ion batteries (SIBs) have gained significant attention due to the abundant availability and low cost of sodium. However, the search for high-performance anode materials remains a critical challenge in advancing SIB technology. Based on first-principles swarm-intelligence structure calculations, we propose a metallic 1T′-MoSP monolayer as an anode material that offers a remarkably high storage capacity of 1011 mA h g−1, an ultralow barrier energy of 0.04 eV, and an optimal open-circuit voltage of 0.29 V, ensuring high rate performance and safety. Additionally, the monolayer presents favorable wettability with commonly used SIB electrolytes. Even after adsorbing three-layer Na atoms, the 1T′-MoSP monolayer retains its metallic nature, ensuring excellent electrical conductivity during the battery cycle. These desirable properties make the 1T′-MoSP monolayer a promising anode material for SIBs. [ABSTRACT FROM AUTHOR]

Flexible perovskite solar cells (PSCs) have received great attention due to their low weight, high power ratio, and potential applications in wearable electronic products. The efficiency and stability of flexible PSCs are directly affected by the carrier extraction and transport capabilities of electron transport layer. Herein, efficient flexible PSCs are prepared through incorporating 2,5‐Furandicarboxylic acid (FDCA) multifunctional intermediate layer between tin oxide (SnO2) and perovskite, which can effectively eliminate defects at the interfacial to increase the electron mobility of the SnO2 layer, modify the surface of SnO2 to shift the conduction band upward to improve interface charge extraction, passivate the buried interface of perovskite to induce larger perovskite crystal growth, and establish a bridge between SnO2 and perovskite to improve charge collection efficiency. As a result, the rigid PSCs with FDCA display a champion power conversion efficiency (PCE) of 24.53% with a high open circuit voltage (VOC) of 1.204 V. Furthermore, the flexible device with FDCA achieves a high PCE of 22.10%, and preserve 90% of its initial PCE after aging for 500 h at ambient condition without encapsulation, and maintain 81% of its original PCE after 10,000 bending cycles. [ABSTRACT FROM AUTHOR]

Developing low-cost, high-performance oxygen reduction reaction (ORR) catalysts is crucial for the commercialization of fuel cells and zinc-air batteries. Herein, we report a lignin-derived Fe/N co-doped 3D porous carbon electrocatalyst Fe-NLC-1 as an alternative to commercial Pt/C catalysts, which was synthesized by a green and facile in situ carbonization strategy. Fe-NLC-1 exhibits higher oxygen reduction activity with a half-wave potential (E 1/2) of 0.90 V vs. RHE than commercial 20 wt% Pt/C (E 1/2 = 0.85 V) in the alkaline conditions, as well as excellent methanol tolerance and stability. Furthermore, the Zn-air battery loaded with Fe-NLC-1 exhibits a maximum power density of 125 mW cm−2, an open circuit voltage of 1.477 V, and stable discharge performance, which are comparable or even better than the commercial Pt/C. This study highlights the potential of biomass-derived porous carbon materials for the development of high-performance ORR electrocatalysts. [Display omitted] • Industrial waste lignosulfonate is used to prepare an oxygen reduction catalyst. • The precursor of the porous carbon material is prepared using an in-situ template method. • Fe-NLC-1 with a 3D porous structure has a high specific surface area and excellent ORR performance. [ABSTRACT FROM AUTHOR]

Due to increasing global energy demands and environmental concerns, the search for alternative and environmentally friendly energy sources is of paramount importance. Solid oxide fuel cells (SOFCs) have emerged as a promising solution thanks to their high efficiency and minimal environmental impact. In this regard, perovskite oxides, with their unique properties, have attracted significant attention. This study investigates the dielectric dispersion, electrical features, scaling behavior, and optical defects of Ca 0.67 La 0.22 Ti 0.85 Cr 0.15 O 3 with x = 0.15, CLT 0.85 Cr 0.15. The presence of a vacancy in the A-site is denoted by the square in the formula. Relaxation phenomena were analysed using dielectric and modulus formalism, while the conductivity mechanism was explored through electrical conductivity measurements. The optical defects of CLT 0.85 Cr 0.15 were analysed using electron paramagnetic resonance (EPR) spectroscopy. The findings revealed the formation of Cr3+–VO center defects. These defects serve as sources of in-gap electron traps, thereby enhancing the optical properties of CLT 0.85 Cr 0.15 , making it as a compelling material for various optical applications. The power density increased with temperature, reaching 0.73 W/cm2 at 850 °C, suggesting that CLT 0.85 Cr 0.15 could be a promising electrolyte for IT-SOFCs. The peak in power density correlated with temperature due to thermal effects on ion motion. However, the open circuit voltage decreased with temperature increase, due to increased oxygen vacancies and electron/hole conduction in CLT 0.85 Cr 0.15. The findings suggest that perovskite materials could revolutionize SOFCs technology, paving the way for more efficient and environmentally friendly energy solutions. [ABSTRACT FROM AUTHOR]

Implant treatment is provided to individuals with normal, idealized masticatory forces and also to patients with parafunctional habits such as grinding, clenching, and bruxing. Dental erosion is a common increasing condition and is reported to affect 32 % of adults, increasing with age. This oral environment is conducive to tribocorrosion and the potential loss of materials from the implant surfaces and interfaces with prosthetic components. Although several fretting-corrosion studies have been reported, until now, no study has simulated clinically relevant micromotion. Therefore, our aim is to investigate fretting-corrosion using our new micro-fretting corrosion system, simulating clinical conditions with 5 µm motion at the implant-abutment interface under various occlusal loads and acidic exposures. We simulated four conditions in an oral environment by varying the contact load (83 N and 233 N) and pH levels (3 and 6.5). The commonly used dental implant material, Grade IV titanium, and abutment material Zirconia (ZrO 2)/ Grade IV titanium were selected as testing couple materials. Artificial saliva was employed to represent an oral environment. In addition, a standard tribocorrosion protocol was followed, and the pin was controlled to oscillate on the disk with an amplitude of 5 μ m during the mastication stage. After the testing, 3D profilometry and scanning electron microscopy (SEM) with energy dispersive spectroscopy (EDS) were utilized to analyze the worn surfaces. Inductively coupled plasma mass spectrometry (ICP-MS) was also used to measure the metal ion release. Energy ratios were below 0.2, indicating a fretting regime of partial slip for all groups. Open-circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) were analyzed to compare the electrochemical behavior among groups. As a result, corrosive damage was observed to be more in the Ti4- Ti4 groups than in Zr-Ti4 ones, whereas more mechanical damage was found in the Zr-Ti4 groups than in the Ti4-Ti4 groups. Possible mechanisms were proposed in the discussion to explain these findings. The results observed from this study might be helpful to clinicians with implant selection. For example, for patients with bruxism, a titanium implant paired with a titanium abutment may be preferable, while patients with GERD may benefit more from a titanium implant paired with a zirconia abutment. [Display omitted] [ABSTRACT FROM AUTHOR]

The performance of composite-based triboelectric nanogenerators (C–TENGs) was significantly enhanced through laser surface patterning and graphite coating. The laser etching process produced accurate and consistent patterns, increasing surface area and improving charge accumulation. SEM imagery confirmed the structural differences and enhanced surface properties of the laser-etched C–TENGs. Graphite fibers further augmented the contact surface area, enhancing charge accumulation and diffusion. Experimental results demonstrated that the optimized C–TENGs, especially those with line patterns and graphite coating, achieved a maximal 98.87 V open-circuit voltage (VOC) and a 0.10 µA/cm2 short-circuit current density (JSC) under a 20 N external force. Environmental tests revealed a slight decrease in performance with increased humidity, while long-term stability tests indicated consistent performance over three weeks. Practical application tests showed the potential of C–TENGs integrated into wearable devices, generating sufficient energy for low-power applications, thereby highlighting the promise of these devices for sustainable energy solutions. [ABSTRACT FROM AUTHOR]

Surface modifications not only improve the corrosion resistance of Co-Cr-Mo dental alloys (Bego Wirobond® C) but also ensure their long-term performance and reliability in dental applications. This paper describes the preparation of single-layer TiO2-ZrO2 sol–gel coatings on the Co-Cr-Mo dental alloy using the method of dip-coating. The TiO2-ZrO2 sol–gel coatings were sintered at 300 and 500 °C. SEM analysis shows that sintering at 300 °C produces a uniform, slightly dense structure without micro-cracks, while sintering at 500 °C results in a denser structure with micro-cracks due to higher stress and shrinkage. EDS confirms that sintering temperature affects the elemental composition of the coating, with higher temperatures causing the volatilization or diffusion of Ti and Zr. Roughness measurements indicate that the Ra value increases with the sintering temperature, meeting dental application requirements. Electrochemical measurements by open-circuit potential, EIS, and cyclic potentiodynamic curves demonstrate that sintering temperature and saliva composition affect corrosion resistance, with NaF and mouthwashes (Listerine Total Care Teeth Protection® and Meridol®) generally increasing charge transfer resistance and double-layer capacitance. The ceramic TiO2-ZrO2 coatings significantly reduce pitting corrosion susceptibility at physiological and acidic pH, with the 500 °C sintered coating showing better protective properties. These findings highlight the potential of TiO2-ZrO2 coatings in enhancing the performance of Co-Cr-Mo dental alloys. [ABSTRACT FROM AUTHOR]

Biodegradable implants as bone fixations may present a safe alternative to traditional permanent implants, reducing the risk of infections, promoting bone healing, and eliminating the need for removal surgeries. Structural integrity is an important consideration when choosing an implant material. As a biodegradable implant is being resorbed, until the natural bone has regrown, the implant material needs to provide mechanical stability. However, the corrosive environment of the human body may affect the fatigue life of the material. Conversely, mechanical stress can have an effect on electrochemical corrosion processes. This is known as corrosion fatigue. In the presented work, an experimental setup and methodology was established to analyze the corrosion fatigue of experimental bioresorbable materials while simultaneously monitoring the electrochemical processes. A double-walled measurement cell was constructed for a three-point bending test in Dulbecco's Phosphate-Buffered Saline (DPBS− −), which was used as simulated body fluid (SBF), at 37 ± 1 °C. The setup was combined with a three-electrode setup for corrosion measurements. Rod-shaped zinc samples were used to validate the setup's functionality. Preliminary static and dynamic bending tests were carried out as per the outlined methodology to determine the test parameters. Open-circuit as well as potentiostatic polarization measurements were performed with and without mechanical loading. For the control, fatigue tests were performed in an air environment. The tested zinc samples were inspected via scanning electron microscopy (SEM). Based on the measured mechanical and electrochemical values as well as the SEM images, the effects of the different environments were investigated, and the setup's functionality was verified. An analysis of the data showed that a comprehensive investigation of corrosion fatigue characteristics is feasible with the outlined approach. Therefore, this novel methodology shows great potential for furthering our understanding of the effects of corrosion on the fatigue of biodegradable implant materials. [ABSTRACT FROM AUTHOR]

The power conversion efficiency (PCE) of dye-sensitised solar cells (DSSCs) measures their solar energy conversion performance. With PCEs below 15%, significant energy loss occurs, leading researchers to seek improvements to reduce fossil fuel dependence and enhance DSSCs as an alternative energy source. However, predicting PCE theoretically is challenging due to its dependence on various parameters. In this work, the improved normal model was used to predict the PCE accurately using DFT and TD-DFT of four nanocomposites consisting of catechin natural compound attached to carboxylated graphene quantum dots (GQD) that have been further doped at the centre/edge and decorated with a boronic group. The nanocomposites have been adsorbed on a TiO2 cluster for PCE estimation. This is the first attempt of using decorated GQD with boronic groups in a DSSC and estimating its PCE. The results show that the PCE of catechin improved from 0.077% to the range of 3.96% – 12.61% (B1-CG-C@TiO2 – B2-CG-C@TiO2). This was due to the improved short-circuit current density ($J_{sc}$ J sc ) and fill factor (FF) of all the nanocomposites and the improved open-circuit voltage ($V_{oc}$ V oc ) of all nanocomposites except B1-CG-C@TiO2 in comparison to catechin. This means all the designed nanocomposites are more promising candidates than catechin. Highlights: Adsorption at carboxyl group is the most stable site among hydroxyl and GQD base. The improved normal model gives accurate $V_{oc}$ V oc results. All designed nanocomposites exhibited higher PCEs than isolated catechin. Edged doping exhibited the highest $V_{oc}$ V oc , high $J_{sc}$ J sc , and highest PCE of 12.61%. [ABSTRACT FROM AUTHOR]

In recent years, exploring interactions between sunlight, semiconducting minerals and microorganisms in nature has attracted great attention. However, relatively little research has been conducted on the interaction between minerals and microorganisms in the plain areas of the Yellow River Basin under sunlight. In this study, the mineral composition and microbial community of red soil from the Ningxia Plain, China were analyzed. X–ray diffraction (XRD) results showed that red soil contained semiconducting minerals such as birnessite, hematite and goethite. 16S rRNA analysis found that electroactive microorganisms such as Proteobacteria, Firmicutes and Actinobacteriota were enriched in in–situ microbial community of red soil. Afterwards, electrochemical tests such as linear sweep voltammetry (LSV) and I–t curves, indicated that red soil exhibited good semiconducting properties under light irradiation. Finally, a dual chamber system and electrochemical techniques were used to explore the electron transfer relationship between red soil and microorganisms. The open circuit voltage (350 mV) and maximum power density (1242.72 mW/m2) of red soil cathode system were significantly improved compared to blank graphite electrode, indicating that red soil could serve as electron acceptors for microbial extracellular respiration. Red soil electrode in live bacteria exhibited the highest photocurrent density (0.29 μA/cm2) and the lowest charge transfer resistance (Rct) (223 Ω) under light conditions, indicating that red soil accelerated the rapid transfer of electrons, reduced polarization loss, and enhanced extracellular electron transfer (EET) process under light conditions. This study demonstrated that the participation of semiconducting minerals in microbial EET processes under sunlight in the Ningxia Plain, China. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators (TENGs) made from biocompatible materials serve as promising integrated power sources for portable wearable electronics due to many advantages such as lightweight, high flexibility, simple technique, and excellent breathability. In this work, we report the fabrication of electrospun polycaprolactone micro-nanofiber films (s-PCL) and convex-microdome-patterned polydimethylsiloxane (c-PDMS) utilizing electrospinning and micromolding techniques. These materials, s-PCL and c-PDMS, are utilized as positively and negatively charged tribosurfaces, respectively, in the development of a bioTENG device. The developed TENG device can generate a superior power output of 2 mW with an open-circuit voltage (VOC) of 188 V and short-circuit current (ISC) of 18.5 µA, even under a low triggering frequency of 5 Hz. In addition, TENG possesses outstanding durability and output performance stability over a continuous operation of nearly 16,000 cycles. Furthermore, the TENG demonstrates its capacity to harvest mechanical energy and convert it into electricity, capable of directly illuminating more than 100 LEDs. The electrospun s-PCL- and c-PDMS-based TENG can be considered for self-powdered wearable devices attached to fingers, wrists, feet, and other human body parts. [ABSTRACT FROM AUTHOR]

An analytical study of the effect of gadolinium-doped ceria (GDC) electrolyte parameters on the output voltage, output power, open circuit no-load voltage, and leakage current is carried out for solid oxide fuel cell (SOFC). Conductivity due to both ions and electrons is considered for GDC electrolytes. The model incorporates various polarization losses such as activation overpotential, concentration overpotential, and ohmic potential losses in order to study the effect of electrolyte parameters on output voltage. The output voltage and, hence, the power density obtained from the model closely match the experimental reports, thus validating the model. Subsequently, the open circuit no-load voltage model and no-load leakage current are used to study the effect of electrolyte thickness and electronic conductivity on it during no-load conditions. During loaded condition, the model relating the electronic current with the ionic current is employed to analyze the effect of various SOFC parameters governing the electronic current density. This study will be instrumental in designing SOFC with low leakage current density and high output power in order to enhance the performance of SOFC. [ABSTRACT FROM AUTHOR]

Herein, we reported the synthesis of MnO2/ZIF-8 composite by employing two-step synthetic procedure. The synthesized samples have been characterized by utilizing various sophisticated physicochemical technique such as X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and energy-dispersive X-ray (EDX) spectroscopy. The synthesized MnO2/ZIF-8 has been used as counter electrode (CE) for the fabrication of dye-sensitized solar cells (DSSCs). The effect of annealing temperature was studied, and the highest efficiency of 7.2% with a decent open-circuit voltage (Voc) of 0.77 V was achieved at 200 °C. The obtained efficiency of 7.2% is reasonable in comparison to the platinum (Pt)-based DSSCs (7.4%). This work proposed the construction of Pt-free CE for the development of cost-effective DSSCs with reasonable performance in terms of efficiency. [ABSTRACT FROM AUTHOR]

FeTiO 3 /TiO 2 (FTTO) was successfully synthesized and applied for both electrocatalytic NO reduction reaction (e NORR) and photo-assisted e NORR. By introducing Fe into TiO 2 , a heterojunction of FeTiO 3 /TiO 2 was constructed to enhance the electron transfer capability. The large specific surface area of FTTO can provide more active sites. In the e NORR, the FTTO achieved an NH 3 yield of 2845.82 μg h−1 mg−1 at a voltage of −0.70 V (vs. RHE) in K 2 SO 4 solution, which is 2.04 times that of unmodified TiO 2. In the photo-assisted e NORR, the FTTO photoelectrode showed superior ammonia yield of 4259.97 μg h−1 mg−1, which is 11.74 times of that under exclusive illumination and 1.50 times for e NORR. The Zn–NO battery system, using FTTO as the positive electrode and Zn as the negative electrode, demonstrated an open-circuit voltage (OCV) of 2.15 V vs. Zn and an NH 3 yield of 388.72 μg h−1 mg−1 at a current density of 5 mA cm−2. [ABSTRACT FROM AUTHOR]

Dye-sensitized solar cells (DSSCs) exhibit considerable potential as a promising technology, particularly when addressing the challenge of replacing the costly Platinum (Pt) counter electrode (CE) with economically viable and chemically stable CE materials. This study examines the use of two-dimensional hexagonal-shaped nickel oxide nanosheets substituted with varying mol% of lithium (1, 3, and 5 %) (Li (1–5%)-NiO NSs) as the counter electrodes (CEs) for DSSCs. The facile hydrothermal method was employed for the preparation of NiO and Li (1–5 mol%)-NiO samples. The BET analysis of NiO and Li (1–5%)-NiO indicates that higher concentrations of Li1+ ions in Ni2+ ions sites lead to an increase in the overall surface area of NiO. This leads to an elevated number of exposed electrocatalytic active sites which resulted in enhancing the rate of reduction of I 3 − ions. The cyclic voltammetry (CV) result of 5 mol% of Li substituted NiO (5-LNO) shows outstanding electrocatalytic activity towards the redox reaction of I 3 − / I − redox mediator among the as-prepared CEs. The DSSCs assembled with 5-LNO CE show an excellent power conversion efficiency (η) of 5.84 % with short-circuit current (J s c) of 18.76 mAcm−2, and open-circuit voltage (V o c) of 0.80 V which is higher than Pt-based CE (η of 4.05 % with J s c of 10.16 mAcm−2, and V o c of 0.69 V). The DSSCs fabricated with 5-LNO CE exhibit excellent photovoltaic performance because of their high active surface area and enhanced electrical conductivity. The 5-LNO CE has low cost, significant electrocatalytic activity, less toxicity, and superior device efficiency than NiO, other Li (1–3%)-NiO, and Pt CEs, making it a suitable candidate for Pt-free DSSCs application. [ABSTRACT FROM AUTHOR]

The performance of dye-sensitized solar cells (DSSC) primarily depends upon many factors, such as the thickness of the semiconductor layer at the working electrode, dye/sensitizer concentration, and electrolyte. A methodical study is required in one place to deliberate the impact of all these factors on DSSC performance for better understanding and further advancement of the technology. This work emphasizes optimizing the absorption layer, specifically investigating the relationship between the thickness of the TiO2 layer and the concentration of N719 dye. The objective is to elucidate the interconnected effects of these parameters on the overall performance of the device. Additionally, the optimization of electrolyte composition was done with varying concentrations of additives, such as iodine, 4-tert-butyl-pyridine (TBP), guanidinium thiocyanate (GuNCS), and 1-butyl-3-methylimidazolium iodide (BMII) of electrolyte. Initially, the devices with varying TiO2 absorption layers were fabricated. The efficiency, fill factor (FF), open-circuit voltage (VOC), and short-circuit current (ISC) of devices were studied. The drop in open-circuit voltage (VOC) was noticed with the increase in thickness of the TiO2 layer. The highest efficiency was observed at 7.17% with the device fabricated using 6 absorption layer (17.46 μm) of TiO2, 0.7 mM concentration of N719 dye, and 0.03-M iodine, 0.1-M GuNCS, 0.5-M TBP, and 0.6-M BMII in electrolyte. Future developments in this research could focus on further fine-tuning these parameters for improved efficiency and exploring additional innovations in DSSC technology, ultimately contributing to the advancement of sustainable and efficient solar energy conversion systems. [ABSTRACT FROM AUTHOR]

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The conversion of ambient mechanical vibrations into electricity using piezoelectric nanogenerators (PENGs) has garnered significant attention from researchers over the past few years, in light of its potential in wearable applications. The high flexibility and significant ferroelectricity of poly(vinylidene fluoride) (PVDF) make them the most promising candidates for PENG applications among polymer piezoelectric materials. In the present work, NiO nanoparticles were incorporated in different ratios into a PVDF matrix, and their potential for use in piezoelectric nanogenerators was investigated. The PVDF/NiO (5 wt.%) nanocomposite PENG exhibited the highest electrical output, with a 2.8-fold increase in open-circuit voltage and short-circuit current observed as compared to a bare PVDF-based PENG. However, a further increase in the compositional ratio of NiO led to a decrease in PENG output. The improved piezoelectricity in the PVDF/NiO (5 wt.%) nanocomposite is attributed to the enhanced polar phases and improved ferroelectricity of PVDF. Further confirmation of the improved piezoresponse was explored by measurement of the piezoelectric coefficient (d33) and dielectric study of the nanocomposites. The PENG electrical output was further simulated using the finite elemental method in COMSOL Multiphysics 5.5. The simulated results matched well with the experimental output, which confirmed the improved electrical performance of the PVDF/NiO nanocomposite-based PENGs. The enhanced performance of the nanocomposite PVDF film is attributed to the higher β phase in the PVDF. The efficiency of the PENG devices in motion-sensing applications was also explored. Different output voltage signals corresponding to different movements of the nanocomposite-based PENGs make the device compatible with sensor applications. [ABSTRACT FROM AUTHOR]

This study presents a significant advancement in tandem dye-sensitized solar cells (T-DSSCs) through the strategic synthesis of novel triazatruxene (TAT) sensitizers MS-1 and MS-2. These organic sensitizers demonstrate exceptional light-harvesting capacity and overall performance, pushing the boundaries of power conversion efficiency (PCE) in DSSCs. The MS-1-based DSSCs achieved an impressive PCE of 12.81%, while MS-2 sensitizers reached a notable 10.92%. These efficiencies represent significant improvements over the conventional N719 dye (7.60%), demonstrating the potential of metal-free organic sensitizers in DSSC technology. The key to these noteworthy results lies in the molecular design of the organic sensitizers. The triazatruxene donor segment in the MS-1 and MS-2 dyes, featuring a rigid structure and efficient intramolecular charge transfer (ICT), proved to be a game-changer for photovoltaic properties. Building on these results, we explored an innovative parallel tandem cell (PT-DSSC) configuration. By connecting separate cells containing N719 and MS-1 sensitizers, we achieved a record efficiency of 12.89% with enhanced short-circuit current density (JSC) and open-circuit voltage (VOC)compared to single-dye cells. This study highlights the potential of molecular engineering in organic sensitizers and device optimization to enhance DSSC performance, paving the way for further advancements in solar cell technology. [ABSTRACT FROM AUTHOR]

The introduction of porosity into ferroelectric ceramics can decrease the effective permittivity, thereby enhancing the open circuit voltage and electrical energy generated by the direct piezoelectric effect. However, the decrease in the longitudinal piezoelectric coefficient (d33) with increasing porosity levels currently limiting the range of pore fractions that can be employed. By introducing aligned lamellar pores into (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3, this paper demonstrates an unusual 22–41% enhancement in the d33 compared to its dense counterpart. This unique combination of high d33 and a low permittivity leads to a significantly improved voltage coefficient (g33), energy harvesting figure of merit (FoM33) and electromechanical coupling coefficient (k332$k_{33}^2$). The underlying mechanism for the improved properties is demonstrated to be a synergy between the low defect concentration and high internal polarizing field within the porous lamellar structure. This work provides insights into the design of porous ferroelectrics for applications related to sensors, energy harvesters, and actuators. [ABSTRACT FROM AUTHOR]

This study concerns the development and experimental investigation of Direct Urea-Hydrogen Peroxide Fuel Cells (DUHPFC), with a particular emphasis on electrode preparation using nickel zinc iron oxide coated on stainless steel foil via the electrochemical deposition method, and the performance evaluation of single cells under varying operational conditions is also performed. This electrochemical deposition helps achieve a uniform and stable anode coating, which exhibits the high catalytic activity and stability, resulted in significantly enhanced urea oxidation reaction. The research further identifies an optimal performance for a single cell at 25 °C with 9 M KOH and 0.5 M urea, achieving a peak power density of 46.38 mW/cm2. The single cell demonstrates an open circuit voltage (OCV) of 0.72 V. Both energy and exergy efficiencies are further investigated for the cell performance and found to be 58% and 24%, respectively, at 5 M KOH. The electrochemical impedance spectroscopy (EIS) results reveal a significant reduction in impedance, from 30-Ωcm2 at 25 °C to 15-Ωcm2 at 65 °C, indicating an enhanced ionic conductivity and a reduced resistance. The present study results suggest that optimizing the electrode composition and operational parameters significantly improves the DUHPFC's performance, offering valuable insights for future fuel cell development. [Display omitted] • Urea and H₂O₂ enhance electrochemical reactions in DUHPFC systems. • Nickel zinc iron oxide catalyst boosts urea oxidation and cell efficiency. • Optimizing electrode composition and conditions improves DUHPFC performance. • Temperature and KOH concentration affect urea oxidation and cell efficiency. • Testing confirms the stability and durability of the developed anode. [ABSTRACT FROM AUTHOR]

Barium zirconate doped with 20 mol% Yb (BaZr 0.8 Yb 0.2 O 3-δ , BZYb20) is one of the most promising candidates for use as an electrolyte material in protonic ceramic fuel cells (PCFCs) due to its high proton conductivity and high chemical stability under CO 2 -containing fuel conditions. The long-term durabilities of PCFCs prepared using the BZYb20 electrolyte were evaluated as a function of the current density at 500 and 600 °C over a period of 1000 h. At 600 °C, the internal resistance of the cell increased even under open circuit voltage (OCV) condition. Comparing the voltage lowering rates at a current density of 0.172 A cm−2 based on the current density–voltage curves recorded during the durability tests, rates of 3.0, 5.3, and 9.0%/1000 h were achieved at the OCV, 0.047, and 0.172 A cm−2, respectively. A small amount of Ni elements diffused into the electrolyte from the anode to the cathode side, resulting in the formation of cumulus cloud shapes that corresponded to Ni element segregation at the grain boundaries in the electrolyte layer after long-term durability testing at 0.172 A cm−2. At current densities of 0.047–0.048 A cm−2, the voltage lowering rate at 500 °C was higher than that at 600 °C, with values of 6.0 and 2.6%/1000 h being recorded, respectively. This effect may be due to the higher resistance of the cell at 500 °C compared to that at 600 °C. [ABSTRACT FROM AUTHOR]