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In this work, we, for the first time, observed the remarkable thermoelectric properties of a few high-quality PtSe2 layered films fabricated by a post selenization of Pt thin films. An excellent po...

Cu2ZnSnS4 (CZTS) has demonstrated excellent performance as an anode material for lithium-ion batteries. However, the repeated lithiation and delithiation create a cracking pattern and lead to island formation in the thin-film electrode, resulting in a capacity fading over cycling in lithium-ion batteries (LIB's). In order to control this crack behaviour, we introduce carbon into CZTS thin-films by a hydrothermal method to form CZTS@C composite. CZTS@C significantly reduced the crack pattern formation on the electrode surface as well as improved the conductivity of the CZTS@C electrode. At the early stages of lithiation and delithiation, the volume expansion and contraction of Li–CZTS@C create intra-granular cracking only at the surface level, and it offers a high capacity of about 785 mA h g−1 after 150 cycles at 1000 mA g−1 charging rate, excellent rate capability (942 mA h g−1, 678 mA h g−1 and 435 mA h g−1 at 500 mA g−1, 2000 mA g−1 and 5000 mA g−1), and superior cyclability (925 mA h g−1 even after 200 cycles at 500 mA g−1). The excellent electrochemical performance at high-current rates can be attributed to intra-granular cracking together with carbon coating that provides a short transportation length for both lithium ions and electrons. Moreover, the controlled cracking pattern formation in CZTS@C facilitates faster reaction kinetics, which open up a new solution for the development of high-power thin-film anodes for next-generation LIBs applications.

Most chemical vapor deposition methods for transition metal dichalcogenides use an extremely small amount of precursor to render large single-crystal flakes, which usually causes low coverage of the materials on the substrate. In this study, a self-capping vapor-liquid-solid reaction is proposed to fabricate large-grain, continuous MoS2 films. An intermediate liquid phase-Na2Mo2O7 is formed through a eutectic reaction of MoO3 and NaF, followed by being sulfurized into MoS2. The as-formed MoS2 seeds function as a capping layer that reduces the nucleation density and promotes lateral growth. By tuning the driving force of the reaction, large mono/bilayer (1.1 mm/200 μm) flakes or full-coverage films (with a record-high average grain size of 450 μm) can be grown on centimeter-scale substrates. The field-effect transistors fabricated from the full-coverage films show high mobility (33 and 49 cm2 V−1 s−1 for the mono and bilayer regions) and on/off ratio (1 ~ 5 × 108) across a 1.5 cm × 1.5 cm region., Here, the authors develop a self-capping vapour-liquid-solid reaction to fabricate large-grain continuous MoS2 films, whereby an intermediate liquid phase-Na2Mo2O7 is formed through a eutectic reaction of MoO3 and NaF, followed by sulphurisation into MoS2.

The mechanisms for O2 reduction and H2O/H2O2 formation on Co–corrin and Co–porphyrin cathode surfaces of the proton exchange membrane fuel cell (PEMFC) systems have been studied by hybrid Hartree–F...

In addition to the Ge-vacancy control of GeTe, the antimony (Sb) substitution of GeTe for the improvement of thermoelectric performance is explored for Ge1−xSbxTe with x = 0.08–0.12. The concomitant carrier concentration (n) and the aliovalent Sb ion substitution led to an optimal doping level of x = 0.10 to show ZT ∼ 2.35 near ∼800 K, which is significantly higher than those single- and multi-element substitution studies of the GeTe system reported in the literature. In addition, Ge0.9Sb0.1Te demonstrates an impressively high power factor of ∼36 μW cm−1 K−2 and a low thermal conductivity of ∼1.1 W m−1 K−1 at 800 K. The enhanced ZT level for Ge0.9Sb0.1Te is explained through a systematic investigation of micro-structural change and strain analysis from room temperature to 800 K. A significant reduction of lattice thermal conductivity (κlat) is identified and explained by the Sb substitution-introduced strained and widened domain boundaries for the herringbone domain structure of Ge0.9Sb0.1Te. The Sb substitution created multiple forms of strain near the defect centre, the herringbone domain structure, and widened tensile/compressive domain boundaries to support phonon scattering that covers a wide frequency range of the phonon spectrum to reduce lattice thermal conductivity effectively.

Recent advances in nanotechnology, especially the development of integrated nanostructured materials, have offered unprecedented opportunities for photocatalytic CO2 reduction. Compared to bulk semiconductor photocatalysts, most of these nanostructured photocatalysts offer at least one advantage in areas such as photogenerated carrier kinetics, light absorption, and active surface area, supporting improved photochemical reaction efficiencies. In this review, we briefly cover the cutting-edge research activities in the area of integrated nanostructured catalysts for photochemical CO2 reduction, including aqueous and gas-phase reactions. Primarily explored are the basic principles of tailor-made nanostructured composite photocatalysts and how nanostructuring influences photochemical performance. Specifically, we summarize the recent developments related to integrated nanostructured materials for photocatalytic CO2 reduction, mainly in the following five categories: carbon-based nano-architectures, metal-organic frameworks, covalent-organic frameworks, conjugated porous polymers, and layered double hydroxide-based inorganic hybrids. Besides the technical aspects of nanostructure-enhanced catalytic performance in photochemical CO2 reduction, some future research trends and promising strategies are addressed.

Germanium tellurides and its pseudo binary compounds offer interesting properties that are important in thermoelectric and phase-change applications. Despite being a class of materials under scrutiny since its discovery, unique properties and functionalities kept on emerging in recent years. In this work, we observed another unique property of Ge-Sb-Te (GST) thin film that can be beneficial in its development for thermoelectric application. A rapid heating and quenching process of the GST film resulted in a metastable rock-salt cubic structure, exhibiting a unique electronic-transition-like behavior. Above the transition temperature at 150 °C, we observed a temperature-induced band modulation, corroborated with changes in its effective mass and valence band position that leads to favorable electronic and thermoelectric properties. Charge transfer between Sb and Te occurred, accompanied by a distorted cubic-to-cubic structural change. The interplay of the electronic and lattice structure born out of the co...

Interface engineering of CdS/CZTS(Se) is an important aspect of improving the performance of buffer/absorber heterojunction combination. It has been demonstrated that the crossover phenomenon due to the interface recombination can be drastically eliminated by interface modification. Therefore, in-depth studies across the CdS/CZTS(Se) junction properties, as well as effective optimization processes, are very crucial for achieving high-efficiency CZTSSe solar cells. Here, we present a comprehensive study on the effects of soft-baking (SB) temperature on the junction properties and the corresponding optoelectronic and interface-structural properties. Based on in-depth photoemission studies corroborated with structural and composition analysis, we concluded that interdiffusion and intermixing of CZTSSe and CdS phases occurred on the Cu-poor surface of CZTSSe at elevated SB temperatures, and the interface dipole moments induced by electrostatic potential fluctuation were thus significantly eliminated. In contrast, with low SB temperature, the CdS/CZTSSe heterojunction revealed very sharp interface with very short interdiffusion, forming interface dipole moments and drastically deteriorating device performance. These post thermal treatments also significantly suppress defect energy level of interface measured by admittance spectroscopy from 294 to 109 meV due to CdS/CZTSSe interdiffusion. Meanwhile, the interdiffusion effects on the shift of valence band maximum, conduction band minimum and band offset across the heterojunction of thermally treated CdS/CZTSSe interface are spatially resolved at the atomic scale by measuring the local density of states with cross-sectional scanning tunneling microscopy and spectroscopy. A significant enhancement in the power conversion efficiency from 4.88% to 8.48% is achieved by a facile interface engineering process allowing a sufficient intermixing of CdS/Cd and CZTSSe/Se phases without detrimental recombination centers.

Tuning the electronic band structure of black titania to improve photocatalytic performance through conventional band engineering methods has been challenging because of the defect-induced charge carrier and trapping sites. In this study, KSCN-modified hydrogenated nickel nanocluster-modified black TiO2 (SCN–H–Ni–TiO2) exhibits enhanced photocatalytic CO2 reduction due to the interfacial dipole effect. Upon combining the experimental and theoretical simulation approach, the presence of an electrostatic interfacial dipole associated with chemisorption of SCN has dramatic effects on the photocatalyst band structure in SCN–H–Ni–TiO2. An interfacial dipole possesses a more negative zeta potential shift of the isoelectric point from 5.20 to 3.20, which will accelerate the charge carrier separation and electron transfer process. Thiocyanate ion passivation on black TiO2 demonstrated an increased work function around 0.60 eV, which was induced by the interracial dipole effect. Overall, the SCN–H–Ni–TiO2 photocat...

Designing highly conducting metal–organic frameworks (MOFs) is currently a subject of great interest for their potential applications in diverse areas encompassing energy storage and generation. Herein, a strategic design in which a metal–sulfur plane is integrated within a MOF to achieve high electrical conductivity, is successfully demonstrated. The MOF {[Cu2(6-Hmna)(6-mn)]·NH4}n (1, 6-Hmna = 6-mercaptonicotinic acid, 6-mn = 6-mercaptonicotinate), consisting of a two dimensional (–Cu–S–)n plane, is synthesized from the reaction of Cu(NO3)2, and 6,6′-dithiodinicotinic acid via the in situ cleavage of an S–S bond under hydrothermal conditions. A single crystal of the MOF is found to have a low activation energy (6 meV), small bandgap (1.34 eV) and a highest electrical conductivity (10.96 S cm−1) among MOFs for single crystal measurements. This approach provides an ideal roadmap for producing highly conductive MOFs with great potential for applications in batteries, thermoelectric, supercapacitors and related areas.

The quest of earth-abundant bifunctional electrocatalysts for highly efficient oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is essential for clean and renewable energy systems. Herein, directed by the experimental analysis, we demonstrate layered nickel lithium phosphosulfide (NiLiP2S6) crystal as a highly efficient water-splitting catalyst in alkaline media. With strained lattice due to stacked layers as observed by TEM and electronic structure analysis performed by XPS showed mixed Ni2+,3+ oxidation states induced by addition of Li as a cation, NiLiP2S6 displays excellent OER (current density of 10 mA cm–2 showed an overpotential of 303 mV vs. RHE and a Tafel slope of 114 mV dec–1) and HER activity (current density of −10 mA cm–2 showed an overpotential of 184 mV vs. RHE and a Tafel slope of 94.5 mV dec–1). Finally, an alkaline media was employed to demonstrate the overall water splitting using NiLiP2S6 as both the anode and the cathode, which attained a 50 mA cm−2 current density at 1.68 V. This bimetallic phosphosulfide, together with long-term stability and enhanced intrinsic activity, shows enormous potential in water splitting applications.

This work demonstrates the first example of interfacial manipulation in a hybrid photocatalyst based on poly(3-hexylthiophene-2,5-diyl) (P3HT) nanoparticle and graphene oxide (GO) bulk heterojunctions to efficiently reduce CO2 into selective industrial hydrocarbons under gas-phase reaction and visible-light illumination. High selectivity of chemical products (methanol and acetaldehyde) was observed. Moreover, the hybrid photocatalyst’s solar-to-fuel conversion efficiency was 13.5 times higher than that of pure GO. The increased production yield stems from the co-catalytic and sensitizing role of P3HT in the hybrid system due to its ability to extend light absorption to the visible range and improve interfacial charge transfer to GO. The hybrid P3HT-GO formed a type II heterojunction, and its static and dynamic exciton behaviors were examined using fluorescence spectroscopy and exciton lifetime mapping. A reduced fluorescence decay time was observed by interfacial manipulation for improved dispersion, indicating a more efficient charge transfer from the excited P3HT to GO. Thus, the conducting polymer nanoparticles, 2D nanocarbon, have demonstrated superior performance as a metal-free, non-toxic, low-cost, and scalable heterogeneous photocatalyst for CO2 reduction to solar fuel, a solid–gas system.

Layered MoS2 is considered as one of the most promising two-dimensional photocatalytic materials for hydrogen evolution and water splitting; however, the electronic structure at the MoS2-liquid interface is so far insufficiently resolved. Measuring and understanding the band offset at the surfaces of MoS2 are crucial for understanding catalytic reactions and to achieve further improvements in performance. Herein, the heterogeneous charge transfer behavior of MoS2 flakes of various layer numbers and sizes is addressed with high spatial resolution in organic solutions using the ferrocene/ferrocenium (Fc/Fc+) redox pair as a probe in near-field scanning electrochemical microscopy, i.e. in close nm probe-sample proximity. Redox mapping reveals an area and layer dependent reactivity for MoS2 with a detailed insight into the local processes as band offset and confinement of the faradaic current obtained. In combination with additional characterization methods, we deduce a band alignment occurring at the liquid-solid interface., Here, high-resolution atomic force microscopy and scanning electrochemical microscopy are used to investigate the electron transfer behaviour of layered MoS2 flakes in organic solutions, offering insights on the electronic band alignment at the solid-liquid interface.

Chemical alloying is a powerful approach to tune the electronic structure of semiconductors and has led to the synthesis of ternary and quaternary two-dimensional (2D) dichalcogenide semiconductor alloys (e.g., MoSSe₂, WSSe₂, etc.). To date, most of the studies have been focused on determining the chemical composition by evaluating the optical properties, primarily via photoluminescence and reflection spectroscopy of these materials in the 2D monolayer limit. However, a comprehensive study of alloying in multilayer films with direct measurement of electronic structure, combined with first-principles theory, is required for a complete understanding of this promising class of semiconductors. We have combined first-principles density functional theory calculations with experimental characterization of MoS_(2(1-x))Se_(2x) (where x ranges from 0 to 1) alloys using X-ray photoelectron spectroscopy to evaluate the valence and conduction band edge positions in each alloy. Moreover, our observations reveal that the valence band edge energies for molybdenum sulfide/selenide alloys increase as a function of increasing selenium concentration. These experimental results agree well with the results of density functional theory calculations showing a similar trend in calculated valence band edges. Our studies suggest that alloying is an effective technique for tuning the band edges of transition-metal dichalcogenides, with implications for applications such as solar cells and photoelectrochemical devices.

Exploring electrocatalysts composed of earth-abundant elements for a highly efficient hydrogen evolution reaction (HER) is scientifically and technologically important for electrocatalytic water splitting. In this work, we report HER properties of acid treated pyrolyzed vitamin B12 supported on reduced graphene oxide (B12/G800A) that shows an extraordinarily enhanced catalytic activity with low overpotential (115 mV vs. RHE at 10 mA cm−2), which is better than that of most traditional nonprecious metal catalysts in acidic media. Stability tests through long-term potential cycles and at a constant current density confirm the exceptional durability of the catalyst. Notably, the B12/G800A catalyst exhibits extremely high turnover frequencies per cobalt site in acid, for example, 0.85 and 11.46 s−1 at overpotentials of 100 and 200 mV, respectively, which are higher than those reported for other scalable non-precious metal HER catalysts. Moreover, it has been conjectured that the covalency of Co–C and Co–N bonds affects HER activities by comparing the extended X-ray absorption fine structure (EXAFS) spectra of the B12/G800A. High-temperature treatment can modify the Co-corrin structure of B12 to form Co–C bonds along with Co–N, which broadens the band of cobalt, essentially lowering the d-band center from its Fermi level. The lower d-band center leads to a moderate hydrogen binding energy, which is favorable for hydrogen adsorption and desorption.

A highly reproducible sample preparation method for pure GeTe in a rhombohedral structure without converting to the cubic structure up to ∼500 °C is reported to show control of the Ge-vacancy level and the corresponding herringbone-structured microdomains. The thermoelectric figure-of-merit (ZT) for GeTe powder could be raised from ∼0.8 to 1.37 at high temperature (HT) near ∼500 °C by tuning the Ge-vacancy level through the applied reversible in situ route, which made it highly controllable and reproducible. The enhanced ZT of GeTe was found to be strongly correlated with both its significantly increased Seebeck coefficient (∼161 μV K−1 at 500 °C) and reduced thermal conductivity (∼2.62 W m−1 K−1 at 500 °C) for a sample with nearly vacancy-free thicker herringbone-structured microdomains in the suppressed rhombohedral-to-cubic structure phase transformation. The microdomain and crystal structures were identified with HR-TEM (high-resolution transmission electron microscopy) and powder X-ray diffraction (XRD), while electron probe micro-analysis (EPMA) was used to confirm the stoichiometry changes of Ge : Te. Theoretical calculations for GeTe with various Ge-vacancy levels suggested that the Fermi level shifts toward the valence band as a function of increasing the Ge-vacancy level, which is consistent with the increased hole-type carrier concentration (n) and effective mass (m*) deduced from the Hall measurements. The uniquely prepared sample of a near-vacancy-free GeTe in a rhombohedral structure at high temperature favoured an enhanced Seebeck coefficient in view of the converging L- and Σ-bands of the heavy effective mass at the Fermi level, while the high density domain boundaries for the domain of low carrier density were shown to reduce the total thermal conductivity effectively.

Photocatalytic water splitting is a promising way to produce hydrogen fuel from solar energy. In this regard, the search for new photocatalytic materials that can efficiently split water into hydrogen is essential. Here, using first-principles simulations, we demonstrate that the dual-defective SnS2 (Ni-SnS2-VS), by both single-atom nickel doping and sulfur monovacancies, becomes a promising two-dimensional photocatalyst compared with SnS2. The Ni-SnS2-VS monolayer, in particular, exhibits a suitable band alignment that perfectly overcomes the redox potentials for overall water splitting. The dual-defective monolayer displays remarkable photocatalytic activity, a spatially separated carrier, a broadened optical absorption spectrum, and enhanced adsorption energy of H2O. Therefore, the dual-defective SnS2 monolayer can serve as an efficient photocatalyst for overall water splitting to produce hydrogen fuel. Furthermore, a novel dual-defect method can be an effective strategy to enhance the photocatalytic behavior of 2D materials; it may pave inroads in the development of solar-fuel generation.

Nonnoble metal catalysts are low-cost alternatives to Pt for the oxygen reduction reactions (ORRs), which have been studied for various applications in electrocatalytic systems. Among them, transition metal complexes, characterized by a redox-active single-metal-atom with biomimetic ligands, such as pyrolyzed cobalt–nitrogen–carbon (Co–Nx/C), have attracted considerable attention. Therefore, we reported the ORR mechanism of pyrolyzed Vitamin B12 using operando X-ray absorption spectroscopy coupled with electrochemical impedance spectroscopy, which enables operando monitoring of the oxygen binding site on the metal center. Our results revealed the preferential adsorption of oxygen at the Co2+ center, with end-on coordination forming a Co2+-oxo species. Furthermore, the charge transfer mechanism between the catalyst and reactant enables further Co–O species formation. These experimental findings, corroborated with first-principle calculations, provide insight into metal active-site geometry and structural evolution during ORR, which could be used for developing material design strategies for high-performance electrocatalysts for fuel cell applications., Understanding active-site geometry and structural evolution during electrocatalysis is important for further development. Here the authors use operando X-ray absorption spectroscopy combined with electrochemical impedance spectroscopy to investigate single atom catalysts derived from Vitamin B12.

Tin monosulfide (SnS) is a promising light-harvesting material for solar cell applications, owing to its potential for large-scale production, cost-effectiveness, eco-friendly source materials, and long-term stability. However, SnS crystallizes in an orthorhombic structure, which results in a highly anisotropic charge transport behavior. Tailoring the crystallographic orientation of the SnS absorber layer plays a critical role in the enhancement of the transfer of charge carriers and the power conversion efficiency (PCE). By controlling the substrate tilting angle and temperature ramp rate in vapor transport deposition, the crystal growth orientation was tuned to a preferred direction which significantly suppressed the unfavorable (040) crystallographic plane. Through the combination of these two approaches, the PCE could be increased from 0.11% to 2%. The effect of the tilting angle was numerically simulated to investigate its role in controlling the film uniformity and directing the film growth. In addition, the correlation between the texture coefficient of the (040) plane and the charge transport properties was determined by a combination of analytical methods such as device performance studies, electrochemical impedance spectroscopy, along with transient photovoltage, space-charge-limited current, and dark current measurements. These techniques were blended together to prove that the marked improvement in PCE can be ascribed to a reduced charge recombination (in both SnS bulk and interfaces) and an enhanced hole mobility.

In this work, we study the effect of sputtering pressures on the thermoelectric properties of GeTe films. The working pressures were differentiated from 3 to 30 mTorr, and the as-deposited films were annealed at 623 K for 10 min in Ar atmosphere. The results show that the working pressure has a significant effect on the Ge content and crystalline size. The turning trend of the Seebeck coefficient with different sputtering pressures corresponds to the Ge content. The surface morphology of annealed film will change from cracks to voids with increasing sputtering pressure. This behavior can be explained by the growth mechanisms model. The voids and relatively low crystalline size of GeTe films affect to the reduction of the electrical conductivity. In addition, the void content decreased as film thickness was increased. Therefore, controlling the working pressures in the sputtering process and film thickness is important for the thermoelectric performance of GeTe thin film. In our work, we prove that the thermoelectric properties of GeTe films could be optimized effectively by simply tuning different sputtering conditions.

Utilization of g-C3N4 as a single photocatalyst material without combination with other semiconductor remains challenging. Herein, we report a facile green method for synthesizing a metal free modified g-C3N4 photocatalyst. The modification process combines four different strategies in a one-pot thermal reaction: non-metal doping, porosity generation, functionalization with amino groups, and thermal oxidation etching. The as-prepared amino-functionalized ultrathin nanoporous boron-doped g-C3N4 exhibited a high specific surface area of 143.2 m2 g−1 which resulted in abundant adsorption sites for CO2 and water molecules. The surface amino groups act as Lewis basic sites to adsorb acidic CO2 molecules, which can also serve as active sites to facilitate hydrogen generation. Besides, the simultaneous use of ammonium chloride as a dynamic gas bubble template along with thermal oxidation etching efficiently boosts the delamination of the g-C3N4 layers to produce ultrathin sheets; this leads to stronger light–matter interactions and efficient charge generation. Consequently, the newly modified g-C3N4 achieved selective gas-phase CO2 reduction into CO with a production yield of 21.95 µmol g−1, in the absence of any cocatalyst. Moreover, a high hydrogen generation rate of 3800 µmol g-1h−1 and prominent apparent quantum yield of 10.6% were recorded. This work opens up a new avenue to explore different rational modifications of g-C3N4 nanosheets for the efficient production of clean energy.

The present investigation mainly addresses the open circuit voltage (Voc) issue in kesterite based Cu2ZnSn(S,Se)4 solar cells by simply introducing alkali metal fluoride nanolayers (~ several nm NaF, or LiF) to lower the work functions of the front ITO contacts without conventional hole-blocking ZnO layers. Kelvin probe measurements confirmed that the work function of the front ITO decreases from 4.82 to 3.39 and 3.65 eV for NaF and LiF, respectively, resulting in beneficial band alignment for electron collection and/or hole blocking on top electrodes. Moreover, a 10.4% power conversion efficiency (~ 11.5% in the cell effective area) CZTSSe cell with improved Voc of up to 90 mV has been attained. This demonstration may provide a new direction of further boosting the performance of copper chalcogenide based solar cells as well.

A nonstoichiometric Si1− x Ge x with composition ratio dependent saturable absorption prepared by vaporized synthesis and chemical exfoliation is performed to passively mode-lock the Erbium-doped fiber laser (EDFL). The Si1− x Ge x with varied Ge/Si composition ratio from 3 to 16 exhibits tunable nonlinear modulation depth from 17% to 22%, where the Si1− x Ge x with the highest Ge content performs the largest nonlinear modulation depth. When operating the EDFL in the self-amplitude modulation region, the Si1− x Ge x with Ge/Si composition ratios of 3, 9, and 16 self-starts the EDFL pulsation with pulsewidths of 820, 760, and 730 fs. When operating the EDFL in high gain region, the self-phase modulation induced soliton compression dominates the repulsation of passively mode-locked EDFL, which slightly shrinks the EDFL pulsewidth from 346 to 338 fs. All these demonstrations are premier and important to explore the superior nonstoichiometric Si 1− x Ge x saturable absorbers for ultrafast fiber lasers.

Applications of lithium ion battery have been hampered by a lack of ideal anode materials in terms of capacity and stability. The emergence of metal chalcogenide as a candidate material has reinvigorated the search of a low cost and high capacity material system. However, debate about the underlying mechanisms and overall appraisal of its usage in lithium ion battery system remains. Here, a comprehensive study on the energy storage mechanism of copper zinc tin sulfide (CZTS) nanowalls possessing ultrahigh rate capability (500 mAh g−1 charged within 60 s) is reported. Structural evolutions along with the accompanying changes in the oxidation state upon charge/discharge were monitored by ex-situ X-ray diffraction and X-ray photoelectron spectroscopy. During lithiation, lithium ion reacted with CZTS to form lithium sulfides. At the same time, a sequential conversion reactions of copper, zinc and tin sulfides enabled the CZTS nanowalls to achieve excellent electrochemical performance (1400 mAh g−1 at a current density of 1000 mA g−1 over 400 cycles). Multi-element metal chalcogenides in conjunction with an adhesion-enhancing seed layer and a rational nanostructure design hold the key to such ultrahigh capacity and stable anode materials for next generation energy storage devices.

Among the lead-free thermoelectric material, germanium telluride (GeTe) has been extensively investigated due to its high thermoelectric performance (ZT) in mid-temperature; however, high p-type carrier density (∼1021 cm-3) hinder its suitability for higher ZT. In turn, to enhance the thermoelectric performance of the environmentally favorable GeTe, we explored that the Mo doping significantly optimizes the carrier concentration along with uniquely unveiled microcrystalline rods accompanying compact grain boundaries, high-density planar defects, and point defects effectuating all-frequency phonon scattering yields to lower down the thermal conductivity. Furthermore, Sb/Bi co-doping with Mo at the Ge sites predominantly reduces the carrier concentration and thermal conductivity to attain a higher ZT. The co-doping of Bi manifested a more prominent role in achieving the highest ZT of ∼2.3 at 673 K for the sample composition with Ge0.89Mo0.01Bi0.1Te. This study demonstrates an exciting hidden aspect of microstructural modification by forming highly dense microcrystalline rods (MCRs) through Mo and Sb/Bi doping to achieve high-performance in GeTe.

Effects of electronic and atomic structures of V-doped 2D layered SnS2 are studied using X-ray spectroscopy for the development of photocatalytic/photovoltaic applications. Extended X-ray absorption fine structure measurements at V K-edge reveal the presence of VO and VS bonds which form the intercalation of tetrahedral OVS sites in the van der Waals (vdW) gap of SnS2 layers. X-ray absorption near-edge structure (XANES) reveals not only valence state of V dopant in SnS2 is ≈4+ but also the charge transfer (CT) from V to ligands, supported by V Lα,β resonant inelastic X-ray scattering. These results suggest V doping produces extra interlayer covalent interactions and additional conducting channels, which increase the electronic conductivity and CT. This gives rapid transport of photo-excited electrons and effective carrier separation in layered SnS2 . Additionally, valence-band photoemission spectra and S K-edge XANES indicate that the density of states near/at valence-band maximum is shifted to lower binding energy in V-doped SnS2 compare to pristine SnS2 and exhibits band gap shrinkage. These findings support first-principles density functional theory calculations of the interstitially tetrahedral OVS site intercalated in the vdW gap, highlighting the CT from V to ligands in V-doped SnS2 .

Pharmaceutical drugs' removal from wastewater by photocatalytic oxidation process is considered as an attractive approach and environmentally friendly solution. This report aims to appraise the practical application potential of Ag/g-C3N4/ZnO nanorods toward the wastewater treatment of the pharmaceutical industry. The catalysts are synthesized by straightforward and environmentally-friendly strategies. Specifically, g-C3N4/ZnO nanorods heterostructure is constructed by a simple self-assembly method, and then Ag nanoparticles are decorated on g-C3N4/ZnO nanorods by a photoreduction route. The results show that three commercial drugs (paracetamol, amoxicillin, and cefalexin) with high concentration (40 mg L−1) are significantly degraded in the existence of a small dosage of Ag/g-C3N4/ZnO nanorods (0.08 g L−1). The Ag/g-C3N4/ZnO nanorods photocatalyst exhibits degradation performance of paracetamol higher 3.8, 1.8, 1.3 times than pristine g-C3N4, ZnO nanorods, and g-C3N4/ZnO nanorods. Furthermore, Ag/g-C3N4/ZnO nanorods have an excellent reusability and a chemical stability that achieved paracetamol degradation efficiency of 78% and remained chemical structure of the photocatalyst after five cycles. In addition, the photocatalytic mechanism explanation and comparison of photocatalytic drugs’ degradation ability have also been discussed in this study.

Porous α-Fe 2 O 3 nanoparticles are directly grown on acid treated carbon cloth (ACC) using a simple hydrothermal method (denoted as ACC-α-Fe 2 O 3 ) for employment as a flexible and wearable electrochemical electrode. The catalytic activity of ACC-α-Fe 2 O 3 allowing the detection of dopamine (DA) is systematically investigated. The results showed that the ACC-α-Fe 2 O 3 electrode exhibits impressive electrochemical sensitivity, stability and selectivity for the detection of DA. The detection limit determined with the amperometric method appears to be around 50 nM with a linear range of 0.074–113 μM. The impressive DA sensing ability of the as prepared ACC-α-Fe 2 O 3 electrode is due to the good electrochemical behavior and high electroactive surface area (19.96 cm 2 ) of α-Fe 2 O 3 nanoparticles anchored on the highly conductive ACC. It is worth noting that such remarkable sensing properties can be maintained even when the electrode is in a folded configuration.

Photocatalytic formation of hydrocarbons using solar energy via artificial photosynthesis is a highly desirable renewable-energy source for replacing conventional fossil fuels. Using an l-cysteine-based hydrothermal process, here we synthesize a carbon-doped SnS2 (SnS2-C) metal dichalcogenide nanostructure, which exhibits a highly active and selective photocatalytic conversion of CO2 to hydrocarbons under visible-light. The interstitial carbon doping induced microstrain in the SnS2 lattice, resulting in different photophysical properties as compared with undoped SnS2. This SnS2-C photocatalyst significantly enhances the CO2 reduction activity under visible light, attaining a photochemical quantum efficiency of above 0.7%. The SnS2-C photocatalyst represents an important contribution towards high quantum efficiency artificial photosynthesis based on gas phase photocatalytic CO2 reduction under visible light, where the in situ carbon-doped SnS2 nanostructure improves the stability and the light harvesting and charge separation efficiency, and significantly enhances the photocatalytic activity. Photocatalytic reduction of CO2 to hydrocarbons is a promising route to both CO2 utilization and renewable fuel production. Here the authors identify that carbon-doped SnS2 possesses a high catalytic efficiency towards CO2 reduction owing to low photogenerated charge recombination rates.

The thickness of transition metal dichalcogenides (TMDs) plays a key role in enhancing their photocatalytic CO2 reduction activity. However, the optimum thickness of the layered TMDs that is required to achieve sufficient light absorption and excellent crystallinity has still not been definitively determined. In this work, ultra-thin molybdenum disulfide films (MoS2TF) with 25 nm thickness presented remarkable photocatalytic activity, and the product yield increased by about 2.3 times. The photocatalytic mechanism corresponding to the TMDs’ thickness was also proposed. This work demonstrates that the thickness optimization of TMDs provides a cogent direction for the design of high-performance photocatalysts.

A series of Sn added TiS2 (TiS2:Sn x ; x = 0, 0.05, 0.075 and 0.1) were prepared by solid state synthesis with subsequent annealing. The Sn atoms interacted with sulfur atoms in TiS2 and formed a trace amount of misfit layer (SnS)1+m(TiS2−δ)n compound with sulfur deficiency. A significant reduction in electrical resistivity with moderate decrease in the Seebeck coefficient was observed in Sn added TiS2. Hence, a maximum power factor of 1.71 mW/m-K2 at 373 K was obtained in TiS2:Sn0.05. In addition, the thermal conductivity was decreased with Sn addition and reached a minimum value of 2.11 W/m-K at 623 K in TiS2:Sn0.075, due to the impurity phase (misfit phase) and defects (excess Ti) scattering. The zT values increased from 0.08 in pristine TiS2 to an optimized value of 0.46 K at 623 K in TiS2:Sn0.05.

Cu2ZnSnS4 (CZTS) nanoparticles (NPs) were prepared in a one-step microwave-assisted synthesis using a mixture of trioctylphosphine oxide (TOPO) and oleylamine (OLA) as solvent. The reaction medium was optimized by varying the TOPO and OLA ratios to control the CZTS NPs formation. The synthesized CZTS NPs were characterized by X-ray diffraction, Raman spectroscopy, UV–vis spectroscopy, and transmission electron microscopy techniques. High quality CZTS NPs with composition of Cu1.8Zn1.4SnS3.6, optimum size distribution in the range of 22±4 nm and band gap of around 1.5 eV were obtained using microwave assisted synthesis method with OLA:TOPO (1:1) as co-solvent. In the microwave assisted process, the reaction temperature and time has been reduced significantly to 165 °C and 10 min respectively, as compared with other wet chemical solvothermal hot injection/ surfactant based methods. Finally, CZTSSe solar cell fabricated from the selenized microwave-assisted CZTS NPs yielded an efficiency of 4.48%; therefore, the low cost of synthesis of this high quality CZTS NPs ink and the capability of spraying for large solar cell area is very attractive.

The spontaneous formation of surface electron accumulation (SEA) was observed in synthesized molybdenum diselenide (MoSe2) layered crystals with two-hexagonal (2 H) structure. An anomalously high electron concentration at the surface up to 1019 cm−3 is several orders of magnitude higher than that (3.6 × 1012 cm−3) of the inner bulk. The SEA is found to be generated easily by mechanical exfoliation and room temperature deselenization. Se-vacancies have been confirmed to be the major source resulting in SEA and n-type conductivity, and also the active sites for electrochemical catalysis in MoSe2. Noted that the SEA conjugated with the Se-vacancy-related surface defects enhances the electrochemical hydrogen evolution reaction (HER) activity substantially. The optimized HER efficiency with an overpotential at 0.17 V and Tafel slope at 60 mV/dec of the basal plane of 2 H-MoSe2 was achieved by the nitrogen plasma treatment, which has outperformed several nanostructures, thin films, and hybrid counterparts. This study reveals the intriguing surface-dominant electronic property and its effect on the HER enhancement of the basal plane, which is crucial for development of a stable, low-cost and highly efficient catalyst using 2 H-MoSe2.

Exploring an efficient platinum group metal (PGM) free electrocatalyst with superior activity and stability for hydrogen evolution reaction (HER) in a wide pH range is desirable for low-cost hydrogen production. Here, we report atomically dispersed cobalt on nitrogen and sulfur co-doped graphene (N-Co-S/G) for HER. Remarkably, the prepared N-Co-S/G electrocatalyst shows a small overpotential of 67.7 mV vs. reversible hydrogen electrode (RHE) at a current density of 10 mA cm−2 and exceptional durability over 100 h at 10 mA cm−2 under acidic conditions. Moreover, we found that the HER activity of N-Co-S/G is close to 20% Pt/C at all pH levels (0–14) and superior activity at high current density (>100 mA cm−2). Experimental and theoretical calculations reveal that the S atom in N-Co-S/G form Co-S bond, resulting new Co-N3S1 active site, which optimizes Gibbs free energy for hydrogen adsorption (∆GH*) close to zero, while water adsorption and dissociation enhanced by S modulation for neutral and basic media HER.

The controlled growth of metal oxide nanostructures within hierarchically porous conductive carbon-based frameworks is critically important to achieving high volumetric performance and appropriate channel size for energy storage applications. Herein, we grow cobalt oxide (Co3O4) nanoflakes, using a sequential-electrodeposition process, into spherically porous sponge-like few-layer partially reduced graphene oxide (SrGO) synthesized by template-directed ordered assembly. Maximum specific/volumetric capacitances of 1112 F gCo3O4−1 (at 3.3 A gCo3O4−1), 178 F cm−3 (at 2.6 A cm−2), and 406 F gtotal−1 (at 1 A gtotal−1) and sensible rate capability (80% retention by increasing the charge/discharge current from 1 A g−1 to 16 A g−1) are obtained for the Co3O4 nanoflakes@SrGO hybrid electrodes. Besides, an asymmetric supercapacitor is made with the Co3O4[63%]@SrGO[37%] hybrid and activated carbon as a positive and a negative electrode, respectively. Electrochemical results indicate an energy density of 23.3 W h kg−1 at a high power density of 2300 W kg−1 (discharge time of about 42 s) and 62% retention even at a remarkable power density of 36 600 W kg−1 (discharge time of 1.6 s). Moreover, it shows excellent cycling stability with no decay after 20 000 charge/discharge cycles. This performance is attributed to the unique pore-sizes for an ion to channel into the porous structures, conductivity, and mechanical stability of the SrGO framework, which makes it promising for next-generation supercapacitors.

Herein, an electrochemical technique as a cost-effective and one-step approach was utilized to fabricate graphene quantum dots (GQDs). Different amounts of GQDs (0, 0.2, 0.4, 0.8, and 1.2 wt %) were decorated uniformly on the surface of anodized ZnO nanowires (NWs) forming GQD/ZnO NWs. Transmission electron microscopy and atomic force microscopy confirmed formation of GQDs on the ZnO NWs, 12–22 nm in width and 1–3 graphene layers thick. X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy were employed to verify the functional groups on the surface of GQDs, and the results indicated that GQDs readily anchored on the surface of ZnO NWs. The GQD/ZnO NWs exhibited a considerable improvement on the photocatalytic degradation of methylene blue under solar irradiation, due to efficient light absorption. In addition, the results indicated that the optimized GQD (0.4 wt %)/ZnO NWs showed the highest photoactivity with about 3-fold enhancement as compared to pure ZnO NWs. Finally, a mechani...

In this study, we proposed a 4-step selenization process for the RF-sputtered Cu–Zn/Sn metallic stack to prepare Cu2ZnSnSe4 (CZTSe) absorber. We applied a pre-heating treatment for the metal stack under vacuum prior to the selenization, which plays an important role to form a well inter mixed alloy with relatively smooth thin film morphology. The nucleation temperatures were controlled precisely from 150 °C to 500 °C during 4-step selenization to avoid the formation of secondary phases and to improve the crystal quality of CZTSe with a greater homogeneity in the composition. The formation of various phases during each step in 4-step selenization process were studied by X-ray Diffraction, Raman analysis and we proposed a possible reaction mechanism of the CZTSe formation with binary and ternary compounds as intermediates. We also performed optical analysis, including Uv–Visible absorption and low temperature photoluminescence, and scanning transmission electron microscope analysis for the CZTSe samples. Finally, an efficiency of 5.8% CZTSe solar cell is fabricated with an open circuit voltage of 370 mV, short circuit current of 31.99 mA/cm2, and a fill factor of 48.3%.

Kesterite-type Cu 2 ZnSnS 4 (CZTS) has been attracting a lot of attention in thin-film solar cells due to its relatively low cost, earth abundant and environmentally benign nature compared to its analog Cu(In, Ga)Se 2 materials. Until now, solution-based processes are considered as promising methodologies for mass production of CZTS materials for industrial demands. However, most material sources are highly toxic as well as dangerous. In this study, we proposed a facile and green synthesis strategy for the CZTS absorber by taking advantage of an ultrasonic spray technique where we adopted metallic nanopowders and ethanol as our nontoxic precursors as well as solvents, respectively. The phase formation and transition mechanism of the synthesized CZTS film are investigated through varying sulfurization temperatures and analyzed using X-ray diffraction, Raman spectroscopy, and scanning electron microscopy. The solar cell device can be made at a scale as large as 20 × 20 mm 2 , and the cell shows a power conversion efficiency of 1.5%.

We have demonstrated a nonlinear behavior for the bandgap opening of doped graphene by controlling the concentration of B and N co-dopants. X-ray absorption and emission spectra reveal that the ban ...

Phase-change memory materials such as the pseudobinary GeTe-Sb2Te3 compounds have recently gained attention for their good thermoelectric properties, which can be used for power-generation/cooling applications. In this work, GeTe-rich Ge–Sb–Te thin films deposited using a radio-frequency magnetron sputtering method readily exhibit the metastable face-centered cubic (FCC) phase at room temperature. This is in stark contrast to its bulk form, which only transforms to its FCC phase after a transition temperature of around 350 °C. Based on previous works, the FCC phase contributes to the superior thermoelectric properties of this material system. In this study, by decreasing the working deposition pressure, the preferred orientation of (200) plane is observed that translates to improved carrier mobility. Moreover, increasing the annealing temperature has been shown to decrease the carrier concentration due to Te deficiency, leading to a significant improvement in the Seebeck coefficient of the film. By combining these effects, an optimized thermoelectric power factor (21 μW/cm K2) was obtained at an operating temperature of 350 °C.

We present a systematic study in investigating the orientation characteristics of pentacene molecules grown on graphene substrates using polarized Raman spectroscopy. The substrate-induced orientation alignment of pentacene can be well distinguished through the polarized Raman spectra. Interestingly, we found that the nature of polycrystalline graphene not only provides efficient route to control molecular orientation, but also acts as an excellent template allowing conjugated molecules to stack accordingly. The relative orientation of the well-aligned pentacene molecules and the nearby graphene domains exhibits several preferred angles due to atomic interactions. This unique feature is further examined and verified by single domain graphene. Furthermore, polarized Raman spectroscopy contains abundant information allowing us to analyze the ordering level of pentacene films with various thicknesses, which provides insightful perspectives of manipulating molecular orientations with graphene and spatial orga...

A cadmium sulfide (CdS) layer with a thickness of 37±5 nm is deposited onto a Cu2ZnSn(SSe)4 absorber layer using Cd(NO3)2 precursor at pH 11.8 via chemical bath deposition. Full devices fabricated with the thin CdS layer show improved champion efficiency of 6.97%, compared with the 5.91% efficiency of the control device, which can be attributed to the increased current density from reduced light reflection in the visible region and enhanced charge collection in the shorter wavelength region.

Tin-based composites are promising anode materials for high-performance lithium-ion batteries (LIBs); however, insufficient conductivity, as well as fatal volume expansion during cycling lead to poor electrochemical reversibility and cycling stability. In this work, we demonstrate the lithium-ion storage behaviors of SnS2 anode material deposited on different electrode supports. The SnS2 grown on 3D hierarchical carbon nanotube-carbon cloth composites (SnS2-CNT-CC) shows superior capacity retention and cycle stability, compared to that on planar Mo sheets and carbon cloth. The specific capacity of SnS2 on Mo, CC, and CNT-CC is around 240, 840, and 1250 g−1, respectively. The SnS2-CNT-CC electrode outperforms in the cyclic performance and rate capability compared to other electrode configurations due to the multi-electron pathway and high surface area derived from 3D hierarchical CNT-CC electrode support. Furthermore, a significant decrease in the charge transfer resistance is observed by utilizing 3D hierarchical CNT-CC electrode support. The use of 3D hierarchical structures as electrode support could be the best alternative to enhance the electrochemical performances for the next generation LIBs.

The conversion of CO2 into hydrocarbon fuels via the photocatalytic reaction route is considered a potential strategy to concurrently address serious energy crisis and greenhouse gas emission problems. Nevertheless, the generation of long-chain hydrocarbon products (Cn, n ≥ 2) from the visible-light-reactive photocatalytic CO2 reduction has also been considering a contemporary challenge. Herein, we indicate that Ag nanoparticles (Ag NPs) loaded gC3N4/ZnO nanorods heterojunction (Ag-gC3N4/ZnO NRs abbreviation) has extended photoactive range and enhanced specific surface area. The combination of Ag NPs and gC3N4/ZnO NRs significantly enhances photocatalytic CO2 reduction efficiency to form the acetone product. Detail, the acetone production efficiency of Ag-gC3N4/ZnO NRs is 8.4 and 7.5 times higher than pure ZnO NRs and gC3N4/ZnO NRs at the same condition, respectively. This study represents a potential approach toward higher-energy-value hydrocarbons production and greenhouse gas emission mitigation.

BiCuTeO is a promising thermoelectric material owing to its intrinsically low thermal conductivity and high carrier concentration. This study investigated the influence of stoichiometric oxygen deficiencies on the thermoelectric performance of BiCuTeO. Bulk BiCuTeO1−x (0.16 ≥ x) samples were prepared by a conventional solid state reaction and pelleted by hot pressing. Synchrotron X-ray diffraction, electron probe X-ray microanalysis, scanning electron microscopy, and transmission electron microscopy characterized the samples. A maximum value of 1.06 was achieved for the dimensionless figure of merit ZT at 673 K for BiCuTeO0.88, which is approximately 49% better than the current maximal ZT value for BiCuTeO. The power factor was noticeably improved owing to increases in the electrical conductivity and Seebeck coefficient. Moreover, the optimal oxygen deficiency could introduce nanoparticles, resulting in reduced thermal conductivity. The findings will be important for the future development of metal oxide thermoelectric materials for use in practical thermoelectric devices.

Gas-phase photocatalytic reactions to convert carbon dioxide and water into oxygen and hydrocarbons are the foundation of life on earth. However, the efficiency of photosynthesis is relatively low (~1%), which leaves much room for artificial photosynthesis to reach the benchmark of the solar cells (>15%). In this work, carbon implanted SnS2 thin films (C–SnS2) were prepared to study photocatalytic activity and adsorbate-catalyst surface interactions during CO2 photoreduction. The electron density distribution in C–SnS2 and its contribution toward the photogenerated charge transfer process has been analyzed by the angle-dependent X-ray absorption near-edge structure (XANES) study. The C–SnS2 surface affinity toward the CO2 molecule was monitored by in-situ dark current and Raman spectroscopy measurements. By optimizing the dose during ion implantation, SnS2 thin film with 1 wt% carbon incorporation shows 108 times enhancement in the CO2 conversion efficiency and more than 89% product selectivity toward CH4 formation compared with the as-grown SnS2 without carbon incorporation. The improved photocatalytic activity can be ascribed to enhanced light harvesting, pronounced charge-transfer between SnS2 and carbon with improved carrier separation and the availability of highly active carbon sites that serve as favorable CO2 adsorption sites.

Solar photoreduction of CO2 to produce value added hydrocarbons is highly desirable to tackle environmental and energy issues. [1-2] Despite the great improvement in the efficiency and cost of solar cells, the efficiency in artificial photosynthesis is much lower than the >15% of solar cells. Recent progress in 2D chalcogenides with tunable bandgap and layer numbers offers great opportunity for the investigation in this field. In this work, thin film and powder SnS2 have been synthesized for the study. Hydrothermal synthesis of carbon-containing SnS2 exhibits a highly active photocatalytic conversion of CO2 to selective hydrocarbons under visible-light irradiation. Overall, the carbon doping in the SnS2 nanostructure plays a key role and significantly enhance the visible light photocatalytic activity with a photochemical quantum efficiency above 0.7%. [3-4] Meanwhile, Thin film SnS2 has been grown for the mechanism study. By carbon-ion implantation of the thin film, we observed enhanced CO2 reduction under solar illumination. Other FTIR, Raman, NMR, BET, SECM, and synchrotron based facilities including APXPS and XAS have been used to investigate this issue. 1. Shown, H.C. Hsu, Y.C. Chang, C.H. Lin, P.K. Roy, A. Ganguly, C.H. Wang, J.K. Chang, C.I. Wu, L.C. Chen, K.H. Chen, Nano Letters 14, 6097-6103 (2014). 2. Billo, F.Y. Fu, P. Raghunath, I. Shown, W.F. Chen, H.T. Lien, T.H. Shen, J.F. Lee, M. C. Lin, J.S. Hwang, C.H. Lee, L.C. Chen, and K.H. Chen, Small 14, 1702928 (2018). 3. Shown, S. Samireddi, Y.C. Chang, R. Putikam, P.H. Chang, A. Sabbah, F.Y. Fu, W.F. Chen, C.I. Wu, T.Y. Yu, P.W. Chung, M.C. Lin, L.C. Chen, and K.H. Chen, Nature Comm. 9, 169 (2018). 4. Y. Fu, I. Shown, C.H. Li, P. Raghunath, T.Y. Lin, T. Billo, H.L. Wu, C.I. Wu, P.W. Chung, M.C. Lin, L.C. Chen, and K.H. Chen, ACS Appl. Mater. & Interface 11, 28 (2019).

(Invited) Photocatalytic CO2 conversion to hydrocarbon fuels, which makes solar energy harvesting and CO2 reduction reaction (CO2RR) simultaneously, is a killing two birds with one stone approach to solving the energy and environmental problems. However, challenges are the low photon-to-fuel conversion efficiency of the photocatalysts and lack of the product selectivity. Recently, 2D-layered nanomaterials with defect engineering, e.g. the carbon interstitial-doped SnS2 nanosheets [Nature Comm. 9, 169 (2018)], have shown promise for CO2RR. Here, I will present a different case, MoS2 with vacancies controlled by plasma. Productivity and selectivity of CO2RR were found to be dependent strongly with the different Mo/S ratios of the MoS2 of single to few layers. Orders-of-magnitude enhancement in productivity and selectivity of C2 product over 97% has been obtained. The role and interplay of the defects and the hosting materials, and their effects on the adsorption of CO2 and subsequent CO2RR, studied by the near-ambient pressure X-ray photoemission spectroscopy, along with density functional theory will be discussed.