Search

Carbon nanofibers (CFs) have been widely applied as electrodes for energy storage devices owing to the features of increased contact area between electrodes and electrolyte, and shortened transmission route of electrons. However, the poor electrochemical activity and severe waste of space hinder their further application as supercapacitors electrodes. In this work, MnO 2-x nanoflowers restricted and epitaxial growth in/out carbon nanofibers (MnO 2 /MnO@CF) were prepared as excellent electrode materials for supercapacitors. With the synergistic effect of uniquely designed structure and the introduction of MnO and MnO 2 nanoflowers, the prepared interconnected MnO 2 /MnO@CF electrodes demonstrated satisfactory electrochemical performance. Furthermore, the MnO 2 /MnO@CF//activated carbon (AC) asymmetric supercapacitor offered an outstanding long-term cycle stability. Besides, kinetic analysis of MnO 2 /MnO@CF-90 was conducted and the diffusion-dominated storage mechanism was well-revealed. This concept of "internal and external simultaneous decoration" with different valence states of manganese oxides was proven to improve the electrochemical performance of carbon nanofibers, which could be generalized to the preparation and performance improvement of other fiber-based electrodes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Developing a straightforward and general strategy to regulate the surface microenvironment of a carbon matrix enriched with N/B motifs for efficient atomic utilization and electronic state of metal sites in bifunctional hydrogen production via ammonia-borane hydrolysis (ABH) and water electrolysis is a persistent challenge. Herein, we present a simple, green, and universal approach to fabricate B/N co-doped porous carbons using ammonia-borane (AB) as a triple functional agent, eliminating the need for hazardous and explosive functional agents and complicated procedures. The pyrolysis of AB induces the regulation of the surface microenvironment of the carbon matrix, leading to the formation of abundant surface functional groups, defects, and pore structures. This regulation enhances the efficiency of atom utilization and the electronic state of the active component, resulting in improved bifunctional hydrogen evolution. Among the catalysts, B/N co-doped vulcan carbon (Ru/BNC) with 2.1 wt% Ru loading demonstrates the highest performance in catalytic hydrogen production from ABH, achieving an ultrahigh turnover frequency of 1854 min -1 (depending on the dispersion of Ru). Furthermore, this catalyst shows remarkable electrochemical activity for hydrogen evolution in alkaline water electrolysis with a low overpotential of 31 mV at 10 mA cm -2 . The present study provides a simple, green, and universal method to regulate the surface microenvironment of various carbons with B/N modulators, thereby adjusting the atomic utilization and electronic state of active metals for enhanced bifunctional hydrogen evolution., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Electronic skin (e-skin) inspired by the sensory function of the skin demonstrates broad application prospects in health, medicine, and human-machine interaction. Herein, we developed a self-powered all-fiber bio-inspired e-skin (AFBI E-skin) that integrated functions of antifouling, antibacterial, biocompatibility and breathability. AFBI E-skin was composed of three layers of electrospun nanofibrous films. The superhydrophobic outer layer Poly(vinylidene fluoride)-silica nanofibrous films (PVDF-SiO 2 NFs) possessed antifouling properties against common liquids in daily life and resisted bacterial adhesion. The polyaniline nanofibrous films (PANI NFs) were used as the electrode layer, and it had strong "static" antibacterial capability. Meanwhile, the inner layer Polylactic acid nanofibrous films (PLA NFs) served as a biocompatible substrate. Based on the triboelectric nanogenerator principle, AFBI E-skin not only enabled self-powered sensing but also utilized the generated electrical stimulation for "dynamic" antibacterial. The "dynamic-static" synergistic antibacterial strategy greatly enhanced the antibacterial effect. AFBI E-skin could be used for self-powered motion monitoring to obtain a stable signal output even when water was splashed on its surface. Finally, based on AFBI E-skin, we constructed an ultra-long-range human-machine interaction control system, enabling synchronized hand gestures between human hand and robotic hand in any internet-covered area worldwide theoretically. AFBI E-skin exhibited vast application potential in fields like smart wearable electronics and intelligent robotics., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The precise and controllable preparation of carbon nanomaterials under mild conditions poses a great challenge, especially for metal-catalysed multiphase preparation. This work proposes an efficient method that utilizing high-density ultrasound to enhance the liquid-liquid interfacial reaction system. Iron-doped carbon dots (Fe-CDs) are successfully synthesized in such a normal temperature and atmospheric-pressure reaction condition. It is shown that transient cavitation provides a high-temperature and high-pressure microenvironment for the preparation of Fe-CDs. Moreover, the size of the reactant droplets is reduced from 200.0 ± 17.3 μm to 8.1 ± 2.9 μm owing to the acoustic flow and cavitation effects, which increases the specific surface area of the two reacting phases and improves the mass transfer coefficient by more than 252.0 %. As a result, the yield increases by more than an order of magnitude (from 0.7 ± 0.1 % to 11.9 ± 0.2 %) and the Fe doping rate reaches 20.9 %. The photocatalytic oxidation conversion of 1,4-Dihydropyridine (1,4-DHP) using the obtained Fe-CDs is as high as 98.2 %. This research gives a new approach for the efficient and safe production of Fe-CDs, which is promising for industrial applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Simultaneously enhancing the durability and catalytic performance of metal-nitrogen-carbon (M-N x -C) single-atom catalysts is critical to boost oxygen electrocatalysis for energy conversion and storage, yet it remains a grand challenge. Herein, through the combination of early and late metals, we proposed to enhance the stability and tune the catalytic activity of M-N x -C SACs in oxygen electrocatalysis by their strong interaction with the M 2 'C-type MXene substrate. Our density functional theory (DFT) computations revealed that the strong interaction between "early-late" metal-metal bonds significantly improves thermal and electrochemical stability. Due to considerable charge transfer and shift of the d-band center, the electronic properties of these SACs can be extensively modified, thereby optimizing their adsorption strength with oxygenated intermediates and achieving eight promising bifunctional catalysts for ORR/OER with low overpotentials. More importantly, the constant-potential analysis demonstrated the excellent bifunctional activity of SACs supported on MXene substrate across a broad pH range, especially in strongly alkaline media with record-low overpotentials. Further machine learning analysis shows that the d-band center, the charge of the active site, and the work function of the formed heterojunctions are critical to revealing the ORR/OER activity origin. Our results underscore the vast potential of strong interactions between different metal species in enhancing the durability and catalytic performance of SACs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Unstable cathode/electrolyte interphase and severe interfacial side reaction have long been identified as the main cause for the failure of layered oxide cathode during fast charging and long-term cycling for rechargeable sodium-ion batteries. Here, we report a superionic conductor (Na 3 V 2 (PO 4 ) 3 , NVP) bonding surface strategy for O3-type layered NaNi 1/3 Fe 1/3 Mn 1/3 O 2 (NFM) cathode to suppress electrolyte corrosion and near-surface structure deconstruction, especially at high operating potential. The strong bonding affinity at the NVP/NFM contact interface stabilizes the crystal structure by inhibiting surface parasitic reactions and transition metal dissolution, thus significantly improving the phase change reversibility at high desodiation state and prolonging the lifespan of NFM cathode. Due to the high-electron-conductivity of NFM, the redox activity of NVP is also enhanced to provide additional capacity. Therefore, benefiting from the fast ion transport kinetics and electrochemical Na + -storage activity of NVP, the composite NFM@NVP electrode displays a high initial coulombic efficiency of 95.5 % at 0.1 C and excellent rate capability (100 mAh g -1 at 20 C) within high cutoff voltage of 4.2 V. The optimized cathode also delivers preeminent cyclic stability with ∼80 % capacity retention after 500 cycles at 2 C. This work sheds light on a facile and universal strategy on improving interphase stability to develop fast-charging and sustainable batteries., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

The limited energy density of supercapacitors hampers their widespread application in electronic devices. Metal oxides, employed as electrode materials, suffer from low conductivity and stability, prompting extensive research in recent years to enhance their electrochemical properties. Among these efforts, the construction of core-shell heterostructures and the utilization of oxygen vacancy (V O ) engineering have emerged as pivotal strategies for improving material stability and ion diffusion rates. Herein, core-shell composites comprising NiCo 2 S 4 nanospheres and MnO 2 nanosheets are grown in situ on carbon cloth (CC), forming nanoflower clusters while introducing V O defects through a chemical reduction method. Density functional theory (DFT) results proves that the existence of V O effectively enhances electronic and structural properties of MnO 2 , thereby enhancing capacitive properties. The electrochemical test results show that NiCo 2 S 4 @MnO 2 -V 3 exhibits excellent 1376 F g -1 mass capacitance and 2.06 F cm -2 area capacitance at 1 A g -1 . Moreover, NiCo 2 S 4 @MnO 2 -V 3 //activated carbon (AC) asymmetric supercapacitor (ASC) can achieve an energy density of 39.7 Wh kg -1 at a power density of 775 W kg -1 , and maintains 15.5 Wh kg -1 even at 7749.77 W kg -1 . Capacitance retention is 73.1 % after 10,000 cycles at 5 A g -1 , and coulombic efficiency reaches 100 %, demonstrating satisfactory cycle stability. In addition, the device's excellent flexibility offers broad application prospects in wearable electronic applications., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Electrocatalytic nitrate reduction reaction presents a promising avenue for environmentally friendly ammonia (NH 3 ) synthesis and wastewater treatment. An essential aspect to consider is the meticulous design of electrocatalysts. This study explores the utilization of a Ni-Co alloy nanosheet-decorated three-dimensional titanium dioxide (3D-TiO 2 ) nanobelts electrodeposited on titanium meshes (Ni x Co y @TiO 2 /TM) for efficient electrocatalytic NH 3 production. The optimized Ni 1 Co 3 @TiO 2 /TM electrode achieves a significant NH 3 yield of 676.3 ± 27.1 umol h -1 cm -2 with an impressive Faradaic efficiency (FE) of 95.1 % ± 2.1 % in a 0.1 M KOH solution containing 0.1 M NO 3 - at -0.4 V versus the reversible hydrogen electrode. Additionally, the electrode demonstrates exceptional electrochemical activity for NH 3 synthesis in simulated wastewater, delivering an outstanding NH 3 yield of 751.6 ± 44.3 umol h -1 cm -2 with a FE of 96.8 % ± 0.4 % at the same potential of -0.4 V. Moreover, the electrode exhibits minimal variation in current density, NH 3 yields and FEs throughout the 24-h stability test and the 20-cycle test, demonstrating its excellent stability and durability. This study offers a straightforward electrodeposited approach for the development of 3D-nanostructured alloys as catalysts for NH 3 electrosynthesis from nitrates at room temperature., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Effectively mitigating photocorrosion is paramount for achieving high-efficiency and sustainable hydrogen production through photocatalytic water splitting over CdS. In this work, we develop a morphology engineering strategy with adjustable Cd-S bond energy through a simple chemical bath deposition method to synthesize novel hollow hemispherical CdS (H-CdS). The morphologic structure CdS can be precisely controlled by adjusting the reaction temperature, time and pH. Compared with common morphologies of CdS, H-CdS, with its reinforced Cd-S bonding, exhibits not only improved photocatalytic hydrogen evolution activity (20.04 mmol/g/h) but also exceptional resistance to photocorrosion, resulting in outstanding cyclic stability even without the aid of cocatalysts or the introduction of other semiconductors. Comprehensive characterizations reveal that the photocorrosion resistance of H-CdS stems from the high Cd-S bond strength. Moreover, in-situ infrared spectroscopy confirms alterations in the properties and activities of the various CdS morphologies after photocatalytic reaction due to photocorrosion. We thoroughly describe the relationship among morphology, surface energy, bond energy and photocorrosion resistance. Our findings present a novel strategy for mitigating the photocorrosion of CdS and offer valuable insights for future research on CdS photocatalysts aimed at stable water splitting., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The admire activity, selective and corrosion resistance electrocatalysts for oxygen evolution reaction (OER) are the bottleneck restricting seawater electrolysis owing to the side reactions of chloride ions (Cl - ). Herein, we developed a local amorphous S-modified NiFe-LDH ultrathin nanosheets with large spacing on NiFe foam (la-S-NiFe-LDH/NFF) in-situ via the fast H 2 O 2 assisted etching-anion regulation, resulting in a superior OER catalytic activity for seawater electrolysis. Benefitting from the local amorphous architecture induced by S, enhanced the metal-oxygen covalency, triggered lattice oxygen activity, and reduced the desorption energy of O 2 , the la-S-NiFe-LDH/NFF accelerated the OER progress via the lattice-oxygen-mediated (LOM) mechanism. Additionally, the preferential adsorbed OH - and reconstructed SO 4 2- and enhanced the corrosion resistance for seawater electrolysis. The assembled electrolyzer of Pt/C || la-S-NiFe-LDH/NFF possessed an industrial level of 500 mA cm - and enhanced the corrosion resistance for seawater electrolysis. The assembled electrolyzer of Pt/C || la-S-NiFe-LDH/NFF possessed an industrial level of 500 mA cm -2 at 1.83 V potential for seawater electrolysis, and sustained response for 100 h., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Atomically dispersed iron-nitrogen-carbon (Fe-N 4 -C) catalysts show great promises for the electrocatalytic nitrate (NO 3 - ) reduction to ammonia (NH 3 ). Nevertheless, the microenvironmental engineering of the single Fe active sites for further optimizing the catalytic performance remains a challenge. Herein, we proposed to regulate the coordination environment of single Fe active sites to boost its intrinsic electrocatalytic activity for NO 3 conversion by the incorporation of new heteroatoms, including B, C, O, Si, P, and S. Our results revealed that most of the candidates possess low formation energies, showing great potential for experimental synthesis. Moreover, incorporating heteroatoms effectively modulates the charge redistribution and the d-band center of single Fe active sites, enabling the regulation of the binding strength of nitrogenous intermediates. As a result, the N and C coordinated Fe active site (Fe-N - -to-NH 3 conversion by the incorporation of new heteroatoms, including B, C, O, Si, P, and S. Our results revealed that most of the candidates possess low formation energies, showing great potential for experimental synthesis. Moreover, incorporating heteroatoms effectively modulates the charge redistribution and the d-band center of single Fe active sites, enabling the regulation of the binding strength of nitrogenous intermediates. As a result, the N and C coordinated Fe active site (Fe-N 3 C) exhibits superior catalytic performance for NO 3 - electroreduction with a relatively low limiting potential (-0.13 V) due to its optimal adsorption strength with nitrogenous intermediates induced by its moderate charge and d-band center. Importantly, our experimental measures confirmed such theoretical prediction: a maximum NH 3 yield rate of 21.07 mg h -1 mg cat. -1 and 95.74 % Faradaic efficiency were achieved for NO 3 - electroreduction on Fe-N 3 C catalyst. These findings not only suggest a highly efficient catalyst for nitrate reduction but also provide insight into how to design and prepare electrocatalysts with enhanced catalytic performance., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Electrochemical nitrate reduction to ammonia is a promising alternative strategy for producing valuable ammonia. This prospective route, however, is subject to a slow electrocatalytic rate, which resulted from the weak adsorption and activation of intermediate species, and the low density electron cloud of active centers. To address this issue, we developed a novel approach by doping boron into metal hydroxyl oxides to adjust the electronic structure of active centers, and consequently, led a significant improvement in the Faraday efficiency upto approaching 100 %, as well as an impressive ammonia yield upto approximately 23 mg/h mgcat -1 at -0.6 V vs. reversible hydrogen electrode (RHE). Experimental data in mechanism demonstrate that the doped boron play a crucial role in modulating the local electronic environment surrounding the active sites Co. In situ Raman and FTIR spectra provide evidences that boron facilitates the formation of deoxidation and hydrogenation intermediates. Additionally, density functional theory (DFT) calculations support the notion that boron doping enhances the adsorption capability of intermediates, reduces the reaction barrier, and facilitates the desorption of NH 3 ., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Electricity-driven nitrate (NO 3 - ) to ammonia (NH 3 ) conversion presents a unique opportunity to simultaneously eliminate nitrate from sewage while capturing ammonia. However, the Faradaic efficiency and ammonia yield in this eight-electron process remain unsatisfactory, underscoring the critical need for more effective electrocatalysts. In this study, a RuCo alloy nanosheets electrodeposited on pinewood-derived three-dimensional porous carbon (RuCo@TDC) is introduced as a highly-efficient electrocatalyst for the nitrate reduction reaction. The RuCo@TDC catalyst exhibits superior electrocatalytic performance, achieving the highest NH 3 yield of 2.02 ± 0.11 mmol h -1 cm -2 at -0.6 V versus the reversible hydrogen electrode (vs. RHE) and the highest Faradaic efficiency of 95.7 ± 0.8 % at -0.2 V vs. RHE in an electrolyte mixture of 0.1 M KOH and 0.1 M KNO 3 . Furthermore, the Zn-NO 3 - battery using RuCo@TDC as the cathode provides a maximum power density of 2.46 mW cm -2 and a satisfactory NH 3 yield of 1110 μg h -1 cm -2 ., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Phase change materials (PCMs) offer significant advantages in energy conversion and storage by facilitating the storage and release of thermal energy during phase transition processes. However, challenges such as leakage during PCM phase transitions and poor light absorption properties have constrained their application in the field of photothermal energy storage. In this study, Montmorillonite (Mt) and molybdenum disulfide (MoS 2 ) has been used to design and synthesize hybrid aerogels (MoS 2 /Mt) boasting high mechanical strength and excellent photothermal conversion performance. These aerogels are then used to encapsulate polyethylene glycol (PEG) to prepare composite PCMs with outstanding solar-thermal conversion and storage performances. The results show that the synthesized MoS 2 /Mt-PEG composite PCMs exhibit high enthalpies of melting and solidification of 169.16 J/g and 170.78 J/g, respectively, while the aerogel supporting material has a high compressive modulus of 1.96 MPa. Moreover, the composite material displayed excellent thermal stability and leakage resistance after undergoing 30 melting-cooling cycles. Furthermore, the incorporation of MoS 2 imparted outstanding light absorption properties to the MoS 2 /Mt-PEG composite, resulting in a high light absorption and photothermal conversion-storage efficiency of 93.4 % and 96.47 %, respectively. Synthesized composite PCMs also demonstrate outstanding performance in solar-thermal-electricity conversion, achieving a voltage output of 458 mV under illumination conditions and maintaining a sustainable voltage output even after removing the light source. Thus, the composite PCMs prepared in this work can meet the requirements of high enthalpy, effective leakage prevention, efficient solar-thermal conversion and solar-thermal-electricity conversion performance, thereby presenting potential applications in practical solar energy collection, conversion, and storage., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The development of efficient and multifunctional sonosensitizers is crucial for enhancing the efficacy of sonodynamic therapy (SDT). Herein, we have successfully constructed a CoO x -loaded amorphous metal-organic framework (MOF) UIO-66 (A-UIO-66-CoO x ) sonosensitizer with excellent catalase (CAT)- and glutathione-oxidase (GSH-OXD)-like activities. The A-UIO-66-CoO x exhibits a 2.6-fold increase in singlet oxygen ( 1 O 2 ) generation under ultrasound (US) exposure compared to crystalline UIO-66 sonosensitizer, which is attributed to its superior charge transfer efficiency and consistent oxygen (O 2 ) supply. Additionally, the A-UIO-66-CoO x composite reduces the expression of glutathione peroxidase (GPX4) by depleting glutathione (GSH) through Co 3+ and Co 2+ valence changes. The high levels of highly cytotoxic 1 O 2 and deactivation of GPX4 can lead to lethal lipid peroxidation, resulting in concurrent apoptosis and ferroptosis. Both in vitro and vivo tumor models comprehensively confirmed the enhanced SDT antitumor effect using A-UIO-66-CoO x sonosensitizer. Overall, this study emphasizes the possibility of utilizing amorphization engineering to improve the effectiveness of MOFs-based sonosensitizers for combined cancer therapies., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Lithium-selenium batteries have emerged as a promising alternative to lithium-sulfur batteries due to their high electrical conductivity and comparable volume capacity. However, challenges such as the shuttle effect of polyselenides and high-volume fluctuations hinder their practical implementation. To address these issues, we propose synthesizing Fe-CNT/TiO 2 catalyst through high-temperature sintering of an amalgamated nanoarchitecture of carbon nanotubes decorated metal-organic framework (MOF) and MXene, optimized for efficient selenium hosting, leveraging the distinctive physicochemical properties. The catalytic features inherent in the porous Se@Fe-CNT/TiO 2 nanoarchitecture were instrumental in promoting efficient ion and electron transport, and lithium-polyselenide kinetics, while its inherent porosity could play a crucial role in inhibiting electrode stress during cycling. This nanoarchitecture exhibits remarkable battery performance, retaining 99.7% of theoretical capacity after 425 cycles at 0.5 C rate and demonstrating 95.8% capacity retention after 2000 cycles at 1 C rate, with ∼100% Coulombic efficiency. Additionally, the Se@Fe-CNT/TiO 2 electrode exhibited an impressive recovery of 297.5 mAh/g (97.9%) capacity after undergoing 450 cycles at a charging rate of 10 C and a discharging rate of 1 C. This synergistic integration of MOF- and MXene-derived materials unveils new possibilities for high-performance and durable LSeBs, thus advancing electrochemical energy storage systems., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

Exploring the real force that drives the separation of Coulomb-bound electron-hole pairs in the interface of heterojunction photocatalysts can establish a clear mechanism for efficient solar energy conversion efficiency. Herein, the formation of oxygen vacancy (Ov) and isolated Ti 3+ was precisely regulated at the interface of g-C 3 N 4 /TiO 2 Z-scheme heterojunction (g-C 3 N 4 /Ov-Ti 3+ -TiO 2 ) by optimizing the opening degree of the calcination system, showing excellent production rate of CO and CH 4 from CO 2 photoreduction under visible light. This photocatalytic system also exhibited prominent stability. Combining theoretical calculation and characterization, the introduction of Ov and isolated Ti 3+ on the interface could construct a charge transfer channel to break the forbidden transition of n → π*, improving the separation process of photoexcited electron-hole pairs. The photoexcited electrons weakened the covalent interaction of CO bonds to promote the activation of adsorbed inert CO 2 molecules, significantly reducing the energy barrier of the rate-limiting step during CO 2 reduction. This work demonstrates the great application potential of reasonably regulating heterojunction interface for efficient photocatalytic CO 2 reduction., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The problem limiting the use of hydrogen evolution reactions in industry is the inability of electrocatalysts to operate stably at high current densities, so the development of stable and efficient electrocatalysts is important for hydrogen production by water splitting. By designing a rational interface engineering not only can the problem of limited number of catalytic sites in the catalyst be solved, but also can facilitate electron transfer, thus enhancing the efficiency of water splitting. Here, we designed a two-stage chemical vapour deposition method to construct NiC/Mo 2 C nanorod arrays on nickel foam to enhance the electrocatalytic ability of the catalysts, which exhibited efficient HER catalytic activity due to their special tentacle-like nanorod structure and abundant heterogeneous junction surfaces, which brought about abundant active sites as well as promoted electron transfer capability. The resulting catalysts provide current densities of 10, 100 and 500 mA cm -2 with overpotentials of 31, 153 and 264 mV, and exhibit excellent stability at current densities of 10 mA cm -2 for 200 h. This discovery provides a new idea for the rational design of catalysts with special morphologies., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Inc.)

In this work, a straightforward method for synthesizing fullerene derivatives with tentacle structures has been explored for monitoring environmental humidity, which involves introducing sulfonate onto the fullerenes. The structure and number of polar groups in three fullerene derivatives determined by a series of structural tests greatly affect their hydrophilicity and morphology, resulting in changes in humidity sensitive properties. In particular, the hysteresis and response time of the sensors display a great correlation with hydrophilicity. C 60 -Ho, the best performing derivative of this work, has exhibited high response values (∼3500 times), good linearity (R 2  = 97.3 %), and rapid response/recovery times (0.3/4.4 s), making it suitable for various applications such as non-contact detection of respiration, finger distance, and soil humidity., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Hypothesis: Surface modification of dielectric materials changes the dipole-dipole interactions under electric fields, thereby controlling the electrorheological (ER) response. The introduction of metal oxides onto mica templates and further coating of dyes is expected to simultaneously improve the color clarity and ER performance., Experiments: Dye-coated TiO 2 platelets on mica are synthesized for high-performance colorful ER fluids. A sol-gel method is utilized to grow TiO 2 on mica to prepare precursor light-colored mica/TiO 2 materials, which are coated with appropriate dyes to enhance the vividness as determined by the Commission Internationale de clairage L*a*b* color system. The color expression and color clarity improvement are explained via the light interference effect and the presence of chromophores., Findings: The uniform TiO 2 layers can be obtained under low pH conditions with controlled nucleation kinetics. The addition of dyes to TiO 2 increases the surface area and porosity of ER materials and introduces heteroatoms that act as positive factors. In practical ER applications, dye-coated TiO 2 -based ER fluids exhibit higher ER performances compared with the corresponding light-colored TiO 2 -based ER fluids. The vivid-colored ER fluids could provide an easy selection for a wide range of rheological systems requiring a specific magnitude of stress by confirming the color., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)

Developing high-performance sorbents for volatile organic compounds (VOCs) is urgently required for environmental cleaning and personnel protection. Zirconium-based metal-organic frameworks (Zr-MOFs) have been deemed attractive candidates for gaseous toluene capture due to their superior stability and high adsorption capacity. However, the practical application of powdered Zr-MOFs is hindered by inherent limitations. Here, we report a series of defective UiO-66 metal-organic gels (G66-X) with variable missing linker deficiency by altering the modulator concentration. The defect concentration of the adsorbents has a significant impact on the porosity and gaseous toluene adsorption capacity. Dynamic breakthrough results reveal that G66-9 demonstrates optimal breakthrough time of 336 min/g and uptake amount of 334 mg/g, outperforming those of many other typical toluene adsorbents. The breakthrough times and the uptake capacities dramatically decrease with the increase of adsorption temperature. An outstanding regeneration performance of adsorbents can almost maintain even after five adsorption-desorption cycles., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Anode materials with excellent rate capability, capacity, and cycle life have been a challenge in obtaining cost-effective K-ion batteries (KIBs). Based on the concept of waste recycling, we prepared the S-doped (21.5%) amorphous carbon/carbon quantum dots coupled micro-frame (SCMF) by combining chemical exfoliation and S/Se-assisted carbonization. SCMF exhibited the advantages of integrating amorphous carbon and carbon quantum dots (CQDs). The CQDs serve as fast electron channels, while amorphous carbon can accommodate more large-size K-ions and mitigate volume expansion. In KIBs, SCMF maintained a high reversible capacity (414.0 mAh g -1 , after 100 cycles at 100 mA g -1 ), a good rate capability (224.0 mAh g -1 , 2000 mA g -1 ), and excellent capacity retention (208.9 mAh g -1 , after 2000 cycles at 1000 mA g -1 ). The molecular dynamic simulation revealed that CQDs provided fast electron transport channels and that C, O and S atoms had suitable interactions with K, facilitating potassium storage. Moreover, the potassium-ion capacitor (PIC) assembled from SCMF and activated carbon exhibited stable electrochemical performance, proving its potential for application. The research provided valuable insights into the reuse of biomass waste in new secondary batteries., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Cobalt-based catalysts are one of the preferred materials for effective activation of hydrogen peroxide, and metal element doping and active site dispersion are effective methods to enhance their catalytic activity. In this work, manganese-doped cobalt silicate@diatomite composites with enhanced photo-Fenton-like oxidation performance were prepared and used for degradation of methyl orange (MO) dyes. Experiments showed that manganese doping increased the specific surface area of the samples and decreased the band gap energy of the materials. Moreover, the samples doped with manganese elements had better photo-Fenton-like properties. The degradation of methyl orange by Co0.25MnSi@DE/H 2 O 2 -UV reached more than 95%. In addition, density-functional theory (DFT) calculations showed that the Mn-doped samples were more prone to activate H 2 O 2 than non-manganese-doped samples, and the synergistic effect from using a bimetallic catalyst increased the photo-Fenton oxidation activity in the system. ESR spectroscopy and bursting tests indicated that the possible degradation mechanism consisted of hydroxyl radicals and superoxide radicals generated by the synergistic effect of cobalt ions and manganese under UV radiation. This study thus presents a feasible idea for the preparation of cobalt-based photo-Fenton catalysts that also provides a basis for understanding the catalytic mechanism analysis of other types of bimetallic catalysts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Fabricating a cost-effective yet highly active photocatalyst to reduce CO 2 to CO and oxidize benzyl alcohol to benzaldehyde simultaneously, is challenging. Herein, we construct an S-scheme 0D/2D CsPbBr 3 /TiO 2 heterostructure for bifunctional photocatalysis. An in-situ synthetic route is used, which enables the precise integration between CsPbBr 3 nanocrystals and ultrathin TiO 2 nanosheets exposed with (001) facets (termed as TiO 2 -001), resulting in a tightly coupled heterointerface and desirable band offsets. The as-prepared CsPbBr 3 /TiO 2 -001heterojunctions exhibit boosted charge carrier kinetics, particularly, quick carrier separation/transfer and efficient utilization. Experimental results and theoretical calculations validate the S-scheme route in CsPbBr 3 /TiO 2 -001, which allows the enrichment of strongly conserved electrons-holes at conduction and valence bands of CsPbBr 3 and TiO 2 -001, respectively. Consequently, compared to its counterparts, an excellent bifunctional activity (with 24 h reusability) is realized over CsPbBr 3 /TiO 2 -001, where the production rate of CO and benzaldehyde reach up to 78.06 μmol g -1 h -1 and 1.77 mmol g -1 h -1 respectively, without employing any sacrificial agents. This work highlights the development of perovskite-based heterostructures and describes the efficient harnessing of redox potentials and charge carriers towards combined photocatalytic systems., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Two-dimensional montmorillonite nanosheet (MMTNS) is desirable building block for fabricating multifunctional materials as due to its extraordinary properties. In practical applications, however, the concentration of MMTNS prepared by exfoliation is normally too low to be used for material assembling. The general thermal-concentration method is effective, however, it can be time-consuming and require a lot of energy. In this case, the remarkable dispersion stability of MMTNS is worth noting. Herein, the extraordinary dispersion stability of MMTNS derived from electrostatic and hydration repulsion was firstly revealed by molecular dynamics (MD) simulation, which caused the poor dewatering of MMTNS. Further, based on the surface and structural chemistry of MMTNS, a series of strategies, involving charge and cross-linked structure regulation on the edge surface, as well as electrical double-layer modulation and calcification modification based on the electrolytes, were proposed to inhibit the dispersion and enhance the aggregation of MMTNS. Intriguingly, a novel chemical, Tetraethylenepentamine (TEPA) was applied in the dewatering of MMTNS. The TEPA not only act as a cross-linker to bond with MMTNS into an easy-to-dewatering 3D network structure, but also act as a switch for effortless viscosity tuning. Meanwhile, the dual function of electrolytes for electrical double layer compression and calcification modification of MMTNS was investigated by DLVO theory and structural analyses. This work offers explicit directions for improving the dewatering performance of MMTNS to meet the requirements of practical implementation., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

The combination of upconversion nanoparticles (UCNPs) with porous zeolites could enable the development of multifunctional composites and extend their optical applications in sensing, detection and biomedical monitoring. Herein, a series of high luminescent UCNPs@Zeolites nano-micro composites were constructed via the in situ growth strategy, by taking the low phonon-energy fluoride nanoparticles of NaLnF 4 (Ln = Y, Gd) as doping hosts for Er 3+ /Yb 3+ , desilicated FAUY and ZSM-5 as the target zeolites. Benefiting from the formation of tightly combined interfaces between the UCNPs and the target zeolites that effectively passive the surface defects of UCNPs, three orders of magnitude of improved upconversion emission in maximum was obtained under 980 nm excitation through afterward heat treatment at 400 ℃. Moreover, the pre-exchange of Yb 3+ into target zeolites before the in situ growth of UCNPs is another feasible approach to drastically improve the upconversion emission intensity of the UCNPs@Zeolites nano-micro composites. By taking NaGdF 4 :Yb,Er@DSZSM-5/HT as an example probe, the detection of GA was demonstrated and the detection ability of which is super than that of the corresponding bare NaGdF 4 :Yb,Er UCNPs. This research provided a universal approach to construct the UCNPs@Zeolites nano-micro composites with varied upconversion emission colors simply by choosing activator ions, which therefore indicates wide potential applications., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

A facile method for synthesizing carbon-coated lithium iron phosphate (LiFePO 4 , LFP) and an LFP-based multidimensional nanocarbon composite to enhance the electrochemical performance of lithium-ion batteries is presented herein. Three types of cathode materials are prepared: carbon-coated LFP (LC), carbon-coated LFP with carbon nanotubes (LC@C), and carbon-coated LFP with carbon nanotubes/graphene quantum dots (LC@CG). The electrochemical performances of the LC-nanocarbon composites are compared, and both LC@C and LC@CG show improved electrochemical performance than LC. Compared with both the LC and LC@C electrodes, the LC@CG electrode exhibits the highest specific capacity of 107.1 mA h g -1 under 20C of current density, as well as higher capacities and greater stability over all measured current densities. Moreover, after 300 charge-discharge cycles, the LC@CG electrode exhibits the best stability than the LC and LC@C electrodes. This is attributable to the graphene quantum dots, which enhance the morphological stability of the LC@CG electrode during electrochemical measurements. Our findings suggest that LFP-nanocarbon composites are promising as cathode materials and highlight the potential of graphene quantum dots for improving the stability of cathodes., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Nanozyme-based synergistic catalytic therapies for tumors have attracted extensive research attention. However, the unsatisfactory efficiency and negative impact of the tumor microenvironment (TME) hinder its clinical applications. In this study, we provide an easy method to prepare transition metals loaded onto pyrrolic nitrogen-rich g-C 3 N 4 (PN-g-C 3 N 4 ) for forming metal-N4 sites. This N-rich material effectively transfers electrons from g-C 3 N 4 to metal-N4 sites, promotes the oxidation-reduction reaction of metals with different valence states, and improves material reusability. Under TME conditions, copper ions loaded onto PN-g-C 3 N 4 (Cu-PN-g-C 3 N 4 , CPC) can produce ·OH through a Fenton-like reaction for tumor inhibition. This Fenton-like reaction and tumor cell inhibition can be improved further by a photodynamic effect caused by light irradiation. We introduced upconversion nanoparticles (UCNPs) into CPC to obtain nano-enzymes (UCNPs@Cu-PN-g-C 3 N 4 , UCPC) for effectively penetrating the tissue, which emits light corresponding to the UV absorption region of CPC when excited with 980 nm near-infrared (NIR) light. The nanoplatform can reduce H 2 O 2 concentration upon exposure to NIR light; this induces an increase in dissolved oxygen content and produces a higher supply of reactive oxygen species (ROS) for destroying tumor cells. Owing to the narrow bandgap (1.92 eV) of UCPC under 980 light irradiation, even under the condition of hypoxia, the excited electrons in the conduction band can reduce insoluble O 2 through a single electron transfer process, thus effectively generating O 2 •- . Nanoenzyme materials with catalase properties produce three types of ROS (·OH, O 2 •- and 1 O 2 ) when realizing chemodynamic and photodynamic therapies. An excellent therapeutic effect was established by killing cells in vitro and the tumor-inhibiting effect in vivo, proving that the prepared nanoenzymes have an effective therapeutic effect and that the endogenous synergistic treatment of multiple treatment technologies can be realized., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Although Pt is a widely adopted commercial catalyst for the hydrogen evolution reaction (HER), its practical application is greatly limited by its prohibitive cost and high energy barrier for H 2 O dissociation in alkaline media. Herein, an ultrafine Pt-based catalyst decorated with oxygenophilic Ni-sites is rationally designed and successfully synthesized with Pt 5 (GS) 10 (HGS = l-reduced glutathione) nanocluster precursor. The optimized Ni-decorated Pt catalyst (Ni-Pt-C-500) with ultrafine nanoparticles (about 1.6 nm) exhibits a low overpotential (14.0 mV) at 10 mA cm -2 and a mild Tafel slope of 20.8 mV dec -1 in the HER, which is superior to its undecorated counterpart (Pt-C-500), the commercial 20 wt% Pt/C catalyst and most of the previously reported Pt-based electrocatalysts. Experimental observations and theoretical calculations indicate that H 2 O could be spontaneously adsorbed to Ni-sites of the Ni-Pt-C-500 catalyst. Mechanistic studies reveal that Ni-sites promote HER by accelerating the kinetic of H 2 O cleavage and optimizing the electronic structure of Pt. This work paves a new avenue for designing other ultrafine hybrid electrocatalysts based on metal nanoclusters to enhance catalytic reaction kinetics., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

The p-i heterojunction imbedded underneath the perovskite layer plays a vital role in determining the efficiency and stability of inverted perovskite solar cells (PSCs). We found that poly[bis(4-phenyl) (2,4,6-trimethylphenyl) amine] (PTAA) suffers from the severely chain entanglement resulting in poor contact with perovskite. In this work, PTAA layer was treated by poly[(2,6-(4,8-bis(5-(2-ethylhexylthio)-4-fluorothiophen-2-yl)-benzo[1,2-b:4,5-b'] dithiophene))-alt-(5,5-(1',3'-di-2-thienyl-5',7'-bis(2-ethylhexyl) benzo[1',2'-c:4',5'-c'] dithiophene-4,8-dione)] (PBDB-T-SF) diluted solution in chlorobenzene. PBDB-T-SF, which contains dual carbonyl groups in its backbones and suitable electronic levels, can spontaneously fill the voids in chlorobenzene-washed PTAA (nano-PTAA). This not only promotes the work function of the substrate but also strengthens the coherence between perovskite and the substrate. Blade coated PSC (0.09 cm 2 ) containing PBDB-T-SF (s-PSCs) realized a power conversion efficiency (PCE) of 21.83 %. After aging for more than 2000 h, s-PSCs maintains 88 % of the initial efficiency which is only 59 % for the control devices., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Dual-carbon engineering combines the advantages of graphite and hard carbon, thereby optimizing the potassium storage performance of carbon materials. However, dual-carbon engineering faces challenges balancing specific capacity, capability, and stability. In this study, we present a coordination engineering of Zn-N 4 moieties on dual-carbon through additional P doping, which effectively modulates the symmetric charge distribution around the Zn center. Experimental results and theoretical calculations unveil that additional P doping induces an optimized electronic structure of the Zn-N 4 moieties, thus enhancing K + adsorption. A single-atom Zn metal coordinated with nitrogen and phosphorus reduces the K + diffusion barrier and improves fast K + migration kinetics. Consequently, Zn-NPC@rGO exhibits high reversible specific capacities, excellent rate capability, and impressive cycling stability, and remarkable power and energy densities for potassium-ion capacitors (PICs). This study provides insights into crucial factors for enhancing potassium storage performance., Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Wang Jin reports financial support was provided by the National Natural Science Foundation of China., (Copyright © 2023 Elsevier Inc. All rights reserved.)

In this study, we present a bimetallic ion coexistence encapsulation strategy employing hexadecyl trimethyl ammonium bromide (CTAB) as a mediator to anchor cobalt-nickel (CoNi) bimetals in nitrogen-doped porous carbon cubic nanoboxes (CoNi@NC). The fully encapsulated and uniformly dispersed CoNi nanoparticles with the improved density of active sites help to accelerate the oxygen reduction reaction (ORR) kinetics and provide an efficient charge/mass transport environment. Zinc-air battery (ZAB) equipped CoNi@NC as cathode exhibits an open-circuit voltage of 1.45 V, a specific capacity of 870.0 mAh g -1 , and a power density of 168.8 mW cm -2 . Moreover, the two CoNi@NC-based ZABs in series display a stable discharge specific capacity of 783.0 mAh g -1 , as well as a large peak power density of 387.9 mW cm -2 . This work provides an effective way to tune the dispersion of nanoparticles to boost active sites in nitrogen-doped carbon structure, and enhance the ORR activity of bimetallic catalysts., Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [Tong Xue reports financial support was provided by Natural Science Foundation of Ningxia Province. Bei-Ping Wang reports financial support was provided by Natural Science Foundation of Ningxia Province. Tong Xue reports financial support was provided by West Light Foundation of The Chinese Academy of Sciences. Xiang-Hui Yan reports financial support was provided by Ningxia Key Research and Development Program. Yipu Liu reports financial support was provided by National Natural Science Foundation of China.]., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Electrochemical CO 2 reduction (ECR) through single-atom catalysts (SACs) consisting of transition metals (TMs) anchored on nitrogenated carbon (TM-N-C) has shown promise for carbon neutralization. However, high overpotentials and low selectivity are still issues. Regulating the coordination environment of anchored TM atom is important to address these problems. In this study, we evaluated nonmetal atom (NM = B, O, F, Si, P, S, Cl, As and Se) modified TM (TM = Fe, Co, Ni, Cu and Zn)@N 4 -C catalysts for their ECR to CO performance using density functional theory (DFT) calculations. NM dopants can induce active center distortion and tune electron structure, promoting intermediate formation. Doping heteroatoms can improve ECR to CO activity on Ni and Cu@N 4 but worsen it on Co@N 4 catalysts. Fe@N 4 -F 1 (I), Ni@N 3 -B 1 , Cu@N 4 -O 1 (III), and Zn@N 4 -Cl 1 (II) have excellent activity for ECR to CO, with overpotentials of 0.75, 0.49, 0.43, and 0.15 V, respectively, and improved selectivity. The catalytic performance is related to the intermediate binding strength, as evidenced by d band center, charge density difference, crystal orbital Hamilton population (COHP), and integrated COHP (ICOHP). It is expected that our work can be used as the design principle to guide the synthesis of the high-performance heteroatoms modified SACs for ECR to CO., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.)

The agglomeration of metal-organic frameworks (MOFs) has long been a problem, and achieving stable monodispersity in water remains a great challenge. This paper reports a universal strategy that functionalizes MOFs by using an endogenous bioenzyme namely glucose oxidase (GOx), to achieve stable water monodispersity, and integrates it as a highly efficient nanoplatform for cancer synergistic therapy. Phenolic hydroxyl groups in GOx chain confers robust coordination interactions with MOFs, which not only endows stable monodispersion in water, but also provides many reactive sites for further modification. Silver nanoparticles are uniformly deposited onto MOFs@GOx to achieve high conversion efficiency from near-infrared light to heat, resulting in an effective starvation and photothermal synergistic therapy model. In vitro and in vivo experiments confirm excellent therapeutic effect at very low doses without using any chemotherapeutics. In addition, the nanoplatform generates large amounts of reactive oxygen species, induces heavy cell apoptosis, and demonstrates the first experimental example to effectively inhibit cancer migration. Our universal strategy enables stable monodispersity of various MOFs via GOx functionalization and establishes a non-invasive platform for efficient cancer synergistic therapy., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Solar-driven water purification has been deemed as a cheap, green and renewable technology to mitigate water shortage and pollution. Herein, a biomass aerogel with hydrophilic-hydrophobic Janus structure has been prepared as solar water evaporator, which is achieved by partially modifying hydrothermal-treated loofah sponge (HLS) with reduced graphene oxide (rGO). It's a rare design philosophy that HLS serves as a substrate with large pores and hydrophilic properties to ensure continuous and effective water transport, and the hydrophobic layer with rGO modification guarantees good salt resistance in seawater desalination with high photothermal conversion efficiency. As a result, the obtained Janus aerogel, p-HLS@rGO-12, exhibits impressive solar-driven evaporation rates of 1.75 kg m -2 h -1 and 1.54 kg m -2 h -1 for pure water and seawater respectively, with good cycling stability in the evaporation process. Furthermore, p-HLS@rGO-12 also demonstrates outstanding photothermal degradation of rhodamine B (greater than98.8 % in 2 h) and sterilization of E. coli (nearly 100 % in 2 h). This work offers an unusual approach to achieve highly efficient solar-driven steam generation, seawater desalination, organic pollutant degradation, and water disinfection simultaneously. The prepared Janus biomass aerogel holds great potential application in the field of seawater desalination and wastewater purification., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

The high entropy alloy is a powerful material due to its high hardness, strength, magnetic performance, corrosion resistance, and temperature stability. Moreover, when combined with reduced graphene oxide (rGO), it formed a novel material for electromagnetic (EM) absorption. In this work, monodisperse high entropy alloy nanocrystals combined with rGO to create a new type of high entropy alloy/rGO EM absorption material. A colloidal synthesis strategy was used to prepare high entropy Pt 18 Ni 26 Fe 15 Co 14 Cu 27 nanocrystals with a small size of around 3.3 nm. These nanocrystals then in situ grew uniformly on the surface of rGO to form Pt 18 Ni 26 Fe 15 Co 14 Cu 27 /rGO nanocomposite, which were then characterized and tested for EM absorption performance. Compared to the pure high entropy Pt 18 Ni 26 Fe 15 Co 14 Cu 27 nanocrystals, the composite exhibited an improved EM absorption performance with a minimum reflection loss of -41.8 dB at 4.9 GHz and efficient EM wave absorption up to a bandwidth of 2.5 GHz in the 9.4-11.9 GHz band. This novel high entropy alloy/rGO composite has great potential to be used as an excellent material for EM wave absorption., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

For sustained hydrogen generation from seawater electrolysis, an efficient and specialized catalyst must be designed to cope with the slow anode reaction and chloride ions (Cl - ) corrosion. In this work, an S-modified NiFe-phosphate with hierarchical and hollow microspheres was grown on the NiFe foam skeleton (S-NiFe-Pi/NFF), acting as a bifunctional catalyst to enable industrial-scale seawater electrolysis. The introduction of S distorted the lattice of NiFe-phosphate and regulated the local electronic environment around Ni/Fe active metal, both of which enhanced the electrocatalytic activity. Additionally, the existence of phosphate groups repelled Cl - on the surface and enhanced corrosion resistance, enabling stable long-term operation in seawater. The double-electrode electrolyzer composed of the hollow-structured S-NiFe-Pi/NFF as both cathode and anode exhibited a potential of 1.68 V at 100 mA cm -2 for seawater electrolysis. Particularly, to achieve industrial requirements of 500 mA cm -2 , it only required a low cell voltage of 1.8 V and demonstrated a consistent response over 100 h, which outperformed the pair of Pt/C || IrO 2 . This study provides a feasible idea for the preparation of electrocatalysts that are with both highly activity and corrosion resistance, which is crucial for the implementation of industrial-scale seawater electrolysis., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Anion substitution is a valid strategy to modulate the active sites of the transition metal dichalcogenides (TMDs). Herein, a series of cobalt sulfoselenide nanomeshes (CoS 2(1-x) Se 2x @NC) were synthesized by calcining S/Se power with ultrathin metal-organic framework (MOFs) nanosheets. The vacancy concentration of CoS 2(1-x) Se 2x @NC could be adjusted through changing the ratio of S/Se precursor. Interestingly, CoS1.25Se0.75@NC electrocatalyst possesses the largest vacancy concentration as well as the optimal electrocatalytic performance. CoS 1.25 Se 0.75 @NC delivers an overpotential as low as 134 mV for hydrogen evolution reaction (HER) and 270 mV for oxygen evolution reaction (OER) at the current density of 10 mA cm -2 , respectively. Furthermore, CoS 1.25 Se 0.75 @NC affords a low cell voltage of 1.67 V (at 10 mA cm -2 ) and outstanding cycling stability for overall water splitting reaction (more than 55 h). For HER process, theoretical calculations prove that anion vacancy not only lower the free energy barrier of H 2 O dissociation step but also favor the desorption step of intermediate H*. For OER process, the anion vacancies could modulate the adsorption/desorption free energy of oxygen-containing intermediates. The present work demonstrates a practical approach to modulate the vacancy concentration of cobalt sulfoselenide and provides new ideas for design of efficient non-metal electrocatalysts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Efforts to develop a green, inexpensive and effective adsorbent are crucial for eliminating antibiotics in polluted water. The sorption capacity of the as-prepared polyvinyl alcohol (PVA)-assisted cellulose nanocrystals/SiO 2 (CNCs/SiO 2 ) composite aerogel to ciprofloxacin (CIP) rises with the increase of temperature and initial concentration. Reverse trend of sorption capacity can be found when increasing the adsorbent dosage of adsorbent. The optimal pH value for the sorption is proved to be 4. It's found in the uniaxial compression test that the maximum load that PVA-assisted aerogels can withstand is nearly 100 times than that of non-PVA aerogels. Sorption results confirm that the Pseudo-second order (R 2  = 0.9885) and Langmuir models (R 2  = 0.9959) fit well to sorption kinetics and equilibrium data, respectively. The rate constant differs from the initial concentration of CIP according to the Pseudo-second order model. The composite aerogel sorption capacity of Langmuir (q max ) for CIP was 163.34 mg·g -1 . The thermodynamic studies showed that the sorption process is endothermic with the value of enthalpy change of 41.032 kJ/mol. Hydrogen bonding, π-π interaction, hydrophobic and electrostatic interactions are the dominant mechanisms of CIP sorption by the PVA-assisted CNCs/SiO 2 composite aerogel., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Solar energy is becoming the most promising option to mitigate the energy crisis in the future and can be applied in renewable and economical technologies such as water splitting and pollutants degradation. The promotion of the electronic energetic level is considered an efficient method to enhance the photocatalytic performance of semiconductor materials for solar energy conversion. The highly energetic electrons exhibit a remarkable reduction ability by virtue of the electronic spin polarization, which is associated with the conduction band (CB) position. Thus, the regulation of the CB position due to the redistribution of electrons by means of defect engineering presents potential. Here, a series of titanium-based metal-organic frameworks (Ti-based MOFs) named MIL-125-m% containing different extents of defects are reported to enable photocatalytic activity under simulated sunlight and visible light illumination for remarkably enhanced photocatalytic hydrogen evolution and pollutant degradation. The experimental results illustrated that MIL-125-5 % exhibited a superior photocatalytic hydrogen evolution rate (16507.27 μmol·g -1 ·h -1 ), much higher than that of MIL-125-0 % (1.444 μmol·g -1 ·h -1 ). The excellent photocatalytic performance was attributed to upshift of d-band center, which strengthened the adsorption of H*, facilitating the H 2 evolution reaction. In addition, the degradation rate of MIL-125-5 % was up to twice the original rate, for the highly energetic electrons induced by the CB flexibility alleviated the photoinduced electron recombination in defective MIL-125. The strategy of defect engineering provides a new path to control the flexibility of the CB position by electronic spin polarization on adjustable metal-organic frameworks (MOFs), and the photocatalytic effect is changed accordingly., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

The development of low-cost electrocatalysts with high oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) performance is crucial for devices used to convert and store hydrogen energy. Research on OER and ORR catalysts has attracted a lot of attention. The limited single-functional catalysts can be expanded as bi-functional catalysts to meet the extra requirement of preparing high-performance catalysts. In this study, we prepared Co-ZIF/CNF in which carbon nanofibers uniformly encapsulated Co- nanoparticles by electrospinning and simple pyrolysis. Co-ZIF/CNF contains both CoO x and Co-N y active sites, showing bifunctional activity for OER and ORR. The optimized catalyst Co-ZIF 1.5 /10CNF 2 has a low OER overpotential of 390 mV, an onset potential of 0.93 V and a half-wave potential of 0.85 V of ORR, exhibiting an outstanding OER and ORR catalytic performance. The catalyst retained 87.53 % of its current after 12 h, showing great stability. This paper provides a new strategy for designing and preparing OER and ORR bifunctional catalysts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier Inc.)

Potassium-ion batteries (PIBs) have attracted enormous attention due to the increasing lithium battery cost, but their development is still in the pre-mature stage due to the limited selection of electrodes. Herein, a free-standing current-collector-integrated electrode, composed of mixed-phase WS 2 nanosheets with nitrogen-doped multichannel carbon nanofibers (N-MCNFs) membrane, is reported for high-performance potassium ion batteries anode. Benefiting the unique multichannel carbon nanostructure as a current collector-integrated electrode as well as mixed-phase lamellar structure WS 2 for enhanced potassium ion entry, the 1T/2H-WS 2 /N-MCNFs hybrid current-collector-free anode delivers an outstanding areal capacity of 2.88 mAh cm -2 (corresponding to 411 mAh/g based on the mass of both electrode and current collector) at a current of 0.7 mA cm -2 as well as long-term cycling stability for over 1000 cycles at a high current of 14 mA cm -2 , surpassing the current state-of-art PIB anode. It is believed that our findings based on the high energy current collector integrated electrode at high mass loading would boost future research on practical metal ion batteries., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

All-inorganic lead-free halide double perovskites have emerged as rising star photocatalysts to substitute the toxic lead-based hailed perovskites (LHPs) owing to their unique photophysical properties. Nevertheless, their photocatalytic activities toward CO 2 reduction are still far from comparable with the LHPs, associated with severe charge recombination and sluggish surface catalytic reaction. Herein, a delicate 0D/2D heterojunction of Cs 2 AgBiBr 6 /Bi 2 WO 6 (CABB/BWO) was assembled by in-situ growing cubic CABB nanocrystals on the flat surface of BWO nanosheets via a facile hot-injection method. Density functional theory (DFT) calculations disclose that the work function and Fermi level difference between CABB and BWO give rise to charge redistribution at the interface upon the formation of the heterojunction, creating an internal electric field (IEF). Upon light irradiation, the IEF enables the photogenerated electron transfer from BWO to CABB via direct Z-scheme electron transfer mode with striking spatial charge separation as verified by in-situ X-ray photoelectron (XPS) and electron spin resonance (ESR) spectra. Consequently, the CABB/BWO heterojunction realizes 7-fold higher photocatalytic activity than pristine CABB with significant electron consumption rate of 87.66 µmol g -1 h -1 under simulated solar light (AM 1.5G)., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Modulating the microenvironment of single-metal active sites holds excellent promises for developing highly efficiently oxygen electrocatalysts. Herein, by combining theoretical predictions and experiments, we reported a general strategy to engineer the electronic properties of iron-nitrogen-carbon (FeN 4 /C) catalysts via the incorporation of the boron (B) atom for achieving improved catalytic activity in oxygen electrocatalysis. Our theoretical results revealed that B modulation effectively tunes the d-band center of the iron (Fe) active site to optimize its adsorption strength with oxygenated species, greatly enhancing oxygen reduction reaction (ORR) and oxygen evolution reactions (OER) activity. Our experimental measurements then confirmed the above theoretical predictions: the as-synthesized B-doped FeN 4 /C (Fe-N 4 -B) material can perform as an eligible bifunctional catalyst for ORR and OER in alkaline media, and its catalytic activity even outperforms the commercial noble metal benchmarks. The present findings provide a promising strategy to further design the advanced catalysts for a wide range of electrochemical applications., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Alkaline water electrocatalysis is considered as one of the most reliable method to prepare the stable, inexpensive, and sustainable water splitting catalyst in large-scale. Recently, MoSe 2 attracted great attention as a promising catalyst because of its high electrochemical activity and earth-abundant nature. In this paper, bionic Ni x Se y /MoSe 2 coralline-liked heterogeneous structures were successfully prepared on 3D nickel foam (NF) via a simple solvothermal process complemented by hydrothermal strategy with selenization and alkali treatment. Furthermore, to overcome the less active sites and poor electrical conductivity of MoSe 2 , we learned from the coral structure for the inspiration, and reported a novel hollow rod-like structure with increased active sites. Also, 1 T-2H MoSe 2 improved the electrical conductivity of single phase MoSe 2. We first confirmed the multi-phase of catalyst by XPS analysis with Mo 3d 5/2 splited into two independent regions with the 2H and 1 T phase transition. The optimal ratio of Ni x Se y/ MoSe 2 /NF-5 exhibited excellent electrocatalytic activity towards HER in 1 M KOH, driving current densities of 10, 100 and 200 mA cm -2 at only 76, 165 and 194 mV with stability over 24 h. The work provides new ideas for the construction of transition metal selenides hollow rod array structures of efficient HER electrocatalysts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)