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High performance wide bandgap perovskite solar cell with low V_(OC) deficit less than 0.4 V

Journal of Energy Chemistry 2024年第4期91卷 313-322页

作者： Haikuo Guo Fuhua Hou Xuli Ning Xiaoqi Ren Haoran Yang Rui Liu Tiantian Li Chengjun Zhu Ying Zhao Wei Li Xiaodan Zhang School of Physical Science and Technology Key Laboratory of Semiconductor Photovoltaic Technology and Energy Materials at Universities of Inner Mongolia Autonomous RegionInner Mongolia UniversityHohhot 010021Inner MongoliaChina Institute of Photoelectronic Thin Film Devices and Technology of Nankai University Key Laboratory of Photoelectronic Thin Film Devices and Technology of TianjinSolar Energy Research Center of Nankai UniversityTianjin 300350China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430000HubeiChina

Wide bandgap perovskite solar cells(PSCs)have attracted significant attention because they can be applied to the top cells of tandem solar ***,high open-circuit voltage(V_(OC))deficit(>0.4 V)result from poor crystallization and high non-radiative recombination losses become a serious limitation in the pursuit of high ***,the relevance between different Pbl_(2)proportions and performance parameters are revealed through analysis of surface morphology,residual stress,and *** increase of Pbl_(2)proportion promotes crystal growth and reduces the work function of the perovskite film surface and promotes the energy level alignment with the carrier transport layer,which decreased the V_(OC)***,residual PbI_(2)exacerbated the stress level of perovskite film,and the resulting lattice disorder deteriorated the photostability of the ***,after the synergistic passivation of residual PbI_(2)and PEAI,the V_(OC)achieves 1.266 V and V_(OC)deficit is less than 0.4 V,the record value in wide bandgap PSCs.

关键词： Pb management Perovskite solar cell Strain Wide bandgap Stability

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Garnet-type solid electrolyte:Advances of ionic transport performance and its application in all-solid-state batteries

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Journal of advanced Ceramics 2021年第5期10卷 933-972页

作者： P.M.GONZALEZ PUENTE Shangbin SONG Shiyu CAO Leana Ziwen RANNALTER Ziwen PAN Xing XIANG Qiang SHEN Fei CHEN State Key Lab of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China International School of Materials Science and Engineering Wuhan University of TechnologyWuhan 430070China

All-solid-state lithium batteries(ASSLBs),which use solid electrolytes instead of liquid ones,have become a hot research topic due to their high energy and power density,ability to solve battery safety issues,and capabilities to fulfill the increasing demand for energy storage in electric vehicles and smart grid ***-type solid electrolytes have attracted considerable interest as they meet all the properties of an ideal solid electrolyte for *** garnet-type Li_(7)La_(3)Zr_(2)O_(12)(LLZO)has excellent environmental stability;experiments and computational analyses showed that this solid electrolyte has a high lithium(Li)ionic conductivity(10^(-4)-10^(-3) S·cm^(-1)),an electrochemical window as wide as 6 V,stability against Li metal anode,and compatibility with most of the cathode *** this review,we present the fundamentals of garnet-type solid electrolytes,preparation methods,air stability,some strategies for improving the conductivity based on experimental and computational results,interfacial issues,and finally applications and challenges for future developments of LLZO solid electrolytes for ASSLBs.

关键词： Li_(7)La_(3)Zr_(2)O_(12)(LLZO) solid electrolytes lithium ionic conductivity lithium concentration mobility of lithium-ion air stability solid-state batteries

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Preparation and Thermal Stability of AlMoON Based Solar Selective Absorption Coating

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Journal of Wuhan University of technology(materials Science) 2024年第4期39卷 854-862页

作者：闵捷 YUAN Wenxu CHEN Yufei LAN Yapeng YAN Mengdi LIU Hanze CHENG Xudong 代路 Hubei Provincial Key Laboratory of Green Materials for Light Industry Hubei University of TechnologyWuhan 430068China Col-laborative Innovation Center of Green Light-weight Materials and Processing Hubei University of TechnologyWuhan 430068China School of Materials and Chemical Engineering Hubei University of TechnologyWuhan 430068China School of Industrial Design Hu-bei University of TechnologyWuhan 430068China State Key Laboratory of Advanced Technology for Materials Synthesis and Process-ing Wuhan University of TechnologyWuhan 430070China Science and Technology on Thermal Energy and Power Laboratory Wuhan Second Ship Design&Research InstituteWuhan 430205China

AlMoON based solar selective absorption coatings were deposited on stainless steel substrate by magnetron *** coatings included infrared reflection layer Mo,absorption layer AlMoN,absorption layer AlMoON and antireflection layer AlMoO from bottom to *** surface of the deposited coatings is flat without obvious *** absorptivity and emissivity are 0.896 and 0.09,respectively,and the quality factor is *** heat treatment at 500℃-36 h,the surface roughness of the coating increases,a small number of cracks and other defects appear,and the broken part is still attached to the coating surface.A certain degree of element diffusion occurs in the coatings,resulting in the decline of the optical properties of the *** absorptivity and emissivity are 0.883 and 0.131,respectively,the quality factor is 7.06,and the PC value is *** coatings do not fail under this condition and have certain thermal stability.

关键词： AlMoON coating preparation thermal stability

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Realizing high-voltage aqueous zinc-ion batteries with expanded electrolyte electrochemical stability window

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Chinese Chemical Letters 2023年第2期34卷 129-140页

作者： Buke Wu Yongbiao Mu Zheng Li Ming Li Lin Zeng Tianshou Zhao Shenzhen Key Laboratory of Advanced Energy Storage Southern University of Science and TechnologyShenzhen 518055China Department of Mechanical and Energy Engineering Southern University of Science and TechnologyShenzhen 518055China SUSTech Energy Institute for Carbon Neutrality Southern University of Science and TechnologyShenzhen 518055China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Aqueous zinc-ion batteries(AZIBs) have aroused significant research interest around the world in the past decade. The use of low-cost aqueous electrolytes and a metallic Zn anode with a suitable redox potential and high energy density make AZIBs a potential alternative to commercial Li-ion batteries in the development of next-generation batteries. However, owing to the narrow electrochemical stability window(ESW) of aqueous electrolytes, the choice of cathode materials is limited, because of which AZIBs exhibit a relatively low operating voltage and energy density. Hence, expanding the ESW of aqueous electrolytes is important for the development of practical AZIBs. This paper systematically reviews the electrolyte engineering strategies being explored to broaden the ESW of AZIBs. An in-depth analysis of high-voltage AZIBs is also presented. We suggest that the realization of high-voltage AZIBs depends on the synergistic development of suitable electrolytes and cathode materials. In addition, the cost associated with their fabrication as well as the use of standardized electrochemical tests should be considered during the design of high-voltage AZIBs.

关键词： High voltage Aqueous zinc ion batteries Electrolytes Cathodes Electrochemical stability window

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Revealing the origin of single-atom W activity in H_(2)O_(2) electrocatalytic production:Charge symmetry-breaking

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Carbon Energy 2024年第10期6卷 289-300页

作者： Changfei Jing Junyang Ding Peipei Jia Mengmeng Jin Lihui Zhou Xijun Liu Jun Luo Sheng Dai Institute for New Energy Materials&Low-Carbon Technologies School of Materials Science and EngineeringTianjin University of TechnologyXiqingTianjinChina ShenSi Lab Shenzhen Institute for Advanced StudyUniversity of Electronic Science and Technology of ChinaLonghuaShenzhenChina Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular EngineeringFrontiers Science Center for Materiobiology and Dynamic ChemistryInstitute of Fine ChemicalsSchool of Chemistry and Molecular EngineeringEast China University of Science&TechnologyXuhuiShanghaiChina State Key Laboratory of Featured Metal Materials and Life−cycle Safety for Composite Structures Guangxi Key Laboratory of Processing for Non-ferrous Metals and Featured MaterialsMOE Key Laboratory of New Processing Technology for Nonferrous Metals and MaterialsSchool of ResourcesEnvironment and MaterialsGuangxi UniversityNanningGuangxiChina

The low-energy electrochemical production of hydrogen peroxide(H_(2)O_(2))has garnered significant attention as a viable alternative to traditional industrial routes,with the goal of achieving carbon *** their H_(2)O_(2) selectivity in the two-electron oxygen reduction reaction(ORR),the coordination environment of tungsten(W)-based materials is *** this study,atomically dispersed W single atoms were immobilized on N-doped carbon substrates by a facile pyrolysis method to obtain a W single-atom catalyst(W-SAC).The coordination environment of an isolated W single atom with a tetra-coordinated porphyrin-like structure in W-SAC was determined by X-ray photoelectron spectroscopy and X-ray absorption spectroscopy ***,the as-prepared W-SAC showed superior two-electron ORR activity in 0.1 M KOH solution,including high onset potential(0.89 V),high H_(2)O_(2) selectivity(82.5%),and excellent *** using differential phase contrast-scanning transmission electron microscopy and density functional theory calculations,it is revealed that the charge symmetry-breaking of W atoms changes the adsorption behavior of the intermediates,leading to enhanced reactivity and selectivity for two-electron *** work broadens the avenue for understanding the charge transfer of W-based electrocatalytic materials and the in-depth reaction mechanism of SACs in two-electron ORR.

关键词： charge symmetry-breaking density functional theory scanning transmission electron microscopy tungsten single-atom catalyst two-electron oxygen reduction reaction

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In-situ selective surface engineering of graphene micro-supercapacitor chips

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Nano Research 2022年第2期15卷 1492-1499页

作者： Yiming Chen Minghao Guo Lin Xu Yuyang Cai Xiaocong Tian Xiaobin Liao Zhaoyang Wang Jiashen Meng Xufeng Hong Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200China Faculty of Materials Science&Chemistry China University of GeosciencesWuhan 430074China

Surface modification of graphene oxide(GO)is a powerful strategy to develop its energy density for electrochemical energy ***,pre-modified GO always exhibits unsatisfactory hydrophilia and its ink-relevant utilization is extremely *** GO ink is widely utilized in fabricating micro energy storage devices via extrusion-based 3D-printing,simultaneously obtaining satisfactory hydrophilia and high energy density still remains a *** this work,an in-situ surface engineering strategy was employed to enhance the performance of GO micro-supercapacitor *** dimensionally printed GO micro-supercapacitor chips were treated with pyrrole monomer to achieve selective and spontaneous anchoring of polypyrrole on the microelectrodes without affecting interspaces between the finger *** interface-reinforced graphene scaffolds were edge-welded and exhibited a considerably improved specific capacitance,from 13.6 to 128.4 mF·cm^(-2).These results are expected to provide a new method for improving the performance of micro-supercapacitors derived from GO inks and further strengthen the practicability of 3D printing techniques in fabricating energy storage devices.

关键词： 3D-printing in-situ modification selective surface engineering edge-welded graphene micro-supercapacitors

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Defect engineering in molybdenum-based electrode materials for energy storage

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eScience 2022年第3期2卷 278-294页

作者： Weixiao Wang Fangyu Xiong Shaohua Zhu Jinghui Chen Jun Xie Qinyou An State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan430070China State Key Laboratory of Silicate Materials for Architectures Wuhan University of TechnologyWuhan430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Foshan528200China

Molybdenum-based materials have stepped into the spotlight as promising electrodes for energy storage systems due to their abundant valence states,low cost,and high theoretical ***,the performance of conventional molybdenum-based electrode materials has been limited by slow diffusion dynamics and deficient *** defect engineering to molybdenum-based electrode materials is a viable method for overcoming these intrinsic limitations to realize superior electrochemical performance for energy ***,we systematically review recent progress in defect engineering for molybdenum-based electrode materials,including vacancy modulation,doping engineering,topochemical substitution,and *** particular,the essential optimization mechanisms of defect engineering in molybdenum-based electrode materials are pre-sented:accelerating ion diffusion,enhancing electron transfer,adjusting potential,and maintaining structural *** also discuss the existing challenges and future objectives for defect engineering in molybdenum-based electrode materials to realize high-energy and high-power energy storage devices.

关键词： Energy storage Molybdenum-based electrode materials Defect engineering

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Fast preparation and thermoelectric performance of AgSTe based materials via plasma activated sintering

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materials Chemistry and Physics 2024年 323卷

作者： Melzi, Bachir Yang, Dongwang Zheng, Yu Zhang, Mingqi Jun, Li Cui, JingJing Jia, Yongzhong Pan, Zhicheng Zhong, Shenglong Yan, Yonggao State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China

AgSTe based materials have recently been identified as promising thermoelectric materials that have favorable properties at room temperature. They are usually obtained by conventional processes involving melting, annealing, and sintering, which incur significant energy and time expenditures. The present investigation involved the synthesis of Ag20S7Te3 compounds by a fast non-equilibrium methodology, i.e., plasma activated sintering from raw elemental powders. The monoclinic Ag20S7Te3 phase crystal was successfully formed at a temperature of 673 K, accompanied by the presence of a secondary monoclinic phase, Ag2S. The Ag20S7Te3 phase predominated in the monoclinic form, constituting a significant percentage at temperature of 873 K. Furthermore, the thermoelectric figure of merit (zT) of the AgSTe phase at 873 K was determined to be 0.42. The rapid sample synthesis described herein has the potential to significantly reduce the duration required for material synthesis, hence presenting a conspicuous advantage in the context of manufacturing on a wide scale. © 2024 Elsevier B.V.

关键词： Tellurium compounds

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Nitrogen doped porous carbon-based bifunctional oxygen electrocatalyst with controllab.e phosphorus content for zinc-air battery

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Nano Research 2023年第4期16卷 5887-5893页

作者： Shichang Cai Zihan Meng Gaojie Li Yu An Yapeng Cheng Erjun Kan Bo Ouyang Haining Zhang Haolin Tang School of Material Science and Engineering Henan University of TechnologyZhengzhou 450001China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong LaboratoryXianhu Hydrogen ValleyFoshan 528200China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Applied Physics and Institution of Energy and Microstructure Nanjing University of Science and TechnologyNanjing 210094China

The controllab.e construction of non-noble metal based bifunctional catalysts with high activities towards oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)is of great significance,but remains a ***,we reported an effective method to synthesize cobalt-nitrogen doped mesoporous carbon-based bifunctional oxygen electrocatalyst with controllab.e phosphorus content(Co-N-P_(X)-MC,X=0.5,1.0,1.5,2.0).The mesoporous carbon substrate endowed the asprepared samples with more exposed active surface(236.50 m^(2)·g^(−1))and the most appropriate doping ratio of phosphorus had been investigated to be 1.5(Co-N-P1.5-MC).For ORR,Co-N-P1.5-MC exhibited excellent catalytic activity with more positive onset potential(1.01 V)and half-wave potential(0.84 V)than the other *** OER,Co-N-P1.5-MC also showed a low overpotential of 415 *** experimental results and density-functional theory(DFT)calculations,the outstanding bifunctional catalytic performance of Co-N-P1.5-MC was due to the synergistic cooperation between the P and N dopants,which could reduce the reaction barriers and was favorable for ORR and ***,the Zn-air battery using Co-N-P1.5-MC as the cathode showed remarkable battery performance with high stability(could operate stably for over 160 h at 10 mA·cm^(−2))and maximum power density(119 mW·cm^(−2)),demonstrating its potential for practical *** work could provide significant enlightenment towards the design and construction of bifunctional oxygen electrocatalyst for next-generation electrochemical devices.

关键词： cobalt-nitrogen doped porous carbon phosphorus doping bifunctional electrocatalyst oxygen reduction reaction(ORR)and oxygen evolution reaction(OER) Zn-air battery

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Application of in-situ characterization techniques in modern aqueous batteries

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Rare Metals 2024年第8期43卷 3553-3575页

作者： Jia-Hao Wu Hong-Wei Cai Zhao-Hui Deng Jean-Jacques Gaumet Yu Bao Wen Luo Department of Physics State Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingSchool of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China Laboratoire de Chimie Et Physique:Approche Multi-Echelles Des Milieux Complexes(LCP-A2MC)Institut Jean BarriolUniversitéde Lorraine57070MetzFrance Department of Medicinal Chemistry Hubei College of Chinese MedicineJingzhou 434020China

The development of high-performance aqueous batteries calls for an in-depth knowledge of their chargedischarge redox and failure mechanism,as well as a systematic understanding of the dynamic evolution of microstructure,phase composition,chemical composition,and local chemical environment of the materials for ***-situ characterization technology is expected to understand and reveal the problems faced by aqueous rechargeable batteries,such as the dissolution of electrode materials,the growth of metal negative electrode dendrites,passivation,corrosion,side reactions and a series of *** on this,typical in-situ characterization techniques and their basic mechanisms are summarized,including in-situ optical visualization,in-situ microscopy techniques(in-situ scanning electron microscopy(SEM),in-situ transmission electron microscopy(TEM)),in-situ X-ray techniques(in-situ X-ray diffraction(XRD),in-situ X-ray photoelectron spectroscopy(XPS),in-situ near-edge structural X-ray absorption spectroscopy(XANES)),and in-situ spectroscopy techniques(in-situ Raman spectroscopy,in-situ Fourier transform infrared(FTIR)).Moreover,some emerging techniques concerning aqueous battery research,especially gas evolution and materials dissolution issues,such as in-situ electrochemical quartz crystal microbalance(EQCM).in-situ fiber-optic sensing,in-situ gas chromatography(GC) are *** last,the applications of advanced in-situ characterizations in future research of aqueous batteries are emphasized and discussed,along with some of the remaining challenges and possible solutions.

关键词： Aqueous battery In-situ characterization Phase transformation Solid electrolyte interphase Zinc dendrite growth

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