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Rapid and controllable in-situ self-assembly of main-group metal nanofilms for highly efficient CO_(2)electroreduction to liquid fuel in flow cells

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Nano Research 2024年第6期17卷 5718-5725页

作者： Miao Wang Huaizhu Wang Yaoda Wang Junchuan Liang Mengfei Zhu Jiarui Li Zuoxiu Tie Zhong Jin State Key Laboratory of Coordination Chemistry MOE Key Laboratory of Mesoscopic ChemistryMOE Key Laboratory of High Performance Polymer Materials and TechnologyJiangsu Key Laboratory of Advanced Organic MaterialsTianchang New Materials and Energy Technology Researc

The electrocatalytic reduction of CO_(2)is a promising pathway to generate renewable fuels and ***,its advancement is impeded by the absence of electrocatalysts with both high selectivity and ***,we present a scalable in-situ thermal evaporation technique for synthesizing series of Bi,In,and Sn nanofilms on carbon felt(CF)substrates with a high-aspect-ratio *** resulting main-group metal nanofilms exhibit a homogeneously distributed and highly exposed catalyst surface with ample active sites,thereby promoting mass transport and ad-/desorption of reaction *** from the unique fractal morphology,the Bi nanofilms deposited on CF exhibit optimal catalytic activities for CO_(2)electroreduction among the designed metal nanofilms electrodes,with the highest Faradaic efficiency of 96.9%for formate production at−1.3 V *** hydrogen electrode(RHE)in *** an industrially relevant current density of 221.4 mA·cm−2 in flow cells,the Bi nanofilms retain a high Faradaic efficiency of 81.7%at−1.1 V(***)and a good long-term stability for formate ***,a techno-economic analysis(TEA)model shows the potential commercial viability of electrocatalytic CO_(2)conversion into formate using the Bi nanofilms *** results offer a green and convenient approach for in-situ fabrication of stable and inexpensive thin-film catalysts with a fractal structure applicable to various industrial settings.

关键词： CO_(2)electroreduction non-noble metal nanofilms flow cells efficiency and selectivity techno-economic analysis

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Low-temperature rapid sintering for the fabrication of biphasic Si3N4 ceramics with outstanding mechanical properties

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Journal of advanced Ceramics 2025年第3期14卷 143-150页

作者： Shuo Zhao Songmo Du Shijia Zhang Dengke Zhao Binbin Fan Bohan Wang Fei Li Kexin Chen Guanghua Liu State Key Laboratory of New Ceramic Materials School of Materials Science and EngineeringTsinghua UniversityBeijing 100084China State Key Laboratory for Advanced Metals and Materials University of Science and Technology BeijingBeijing 100083China

The fabrication of Si3N4 ceramics typically requires high temperatures(above 1700℃)and prolonged sintering time to achieve densification,resulting in high energy consumption and increased manufacturing ***,reports on the fabrication of dense Si3N4 ceramics with good mechanical properties under MPa-level pressure and low temperatures are *** this work,we propose a low-temperature rapid spark plasma sintering strategy involving the introduction of fine-grainedβ-Si3N4 powder with high lattice strain energy as an“additive”.Dense biphasic Si3N4 ceramics,predominantlyα-Si3N4,were successfully fabricated at a mechanical pressure of 200 MPa and a temperature of 1300℃,achieving a relative density of 97%.The application of high pressure promoted particle rearrangement and uniform liquid‒phase distribution,providing additional driving forces for *** introduction ofβ-Si3N4 seeds facilitated an in-situ solution–reprecipitation process,enabling rapid densification with a minimal liquid phase and without significant grain growth,resulting in nanometer-scale *** Si3N4 sample prepared at 1350℃ exhibited a desirable combination of high hardness(18.5±0.3 GPa)and fracture toughness(6.7±0.2 MPa·m_(1/2)).The results demonstrate that by adjusting the sintering temperature and time,the phase composition and mechanical properties of the ceramics can be flexibly *** work holds significant potential for industrial manufacturing and provides valuable insights into low-temperature strategies for ceramic fabrication.

关键词： low temperature sintering silicon nitride β-Si3N4 seeds spark plasma sintering(SPS)

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Rare Earth Elements(La,Ce,Pr)Modified Co/NC Catalyst for Efficient and Stable Ammonia Decomposition to Hydrogen Production

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Journal of Wuhan University of technology(Materials Science) 2024年第6期39卷 1372-1378页

作者： ZHU Yi PAN Hongfei State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China National Energy Key Laboratory for New Hydrogen-ammonia Energy Technologies Foshan Xianhu LaboratoryFoshan 528200China

Co/NC catalysts modified with rare earth elements(La,Ce,Pr)were prepared by pyrolysis of rare earth elements doped *** experimental results show that the modification of rare earth elements significantly improves the ammonia decomposition activity and stability of the Co/NC *** La-Co/NC catalyst can achieve an 82.3%ammonia decomposition and 18.4 mmol hydrogen production rate at 550℃with a GHSV of 20000 cm^(3)·h^(-1).Furthermore,no obvious performance degradation is observed after 72 hours of reaction for all rare earth elements modified *** is shown that the modification of rare earth elements significantly improves the surface alkalinity and surface chemical state of the catalyst,and thus improves the ammonia decomposition activity of the catalyst.A new type of high-performance ammonia decomposition Co-based catalyst is proposed,and the promoting effect of rare earth elements on the activity of ammonia decomposition is revealed.

关键词： hydrogen carrier hydrogen production ammonia decomposition rare earth elements cobalt-based catalysts

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Construction of a BiOI/ZnO heterojunction on biomass Juncus effusus fiber for photodegradation of organic pollutants

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Journal of Environmental Sciences 2024年第12期146卷 28-38页

作者： Sijie Zhou Na Zhu Pei Lyu Chunhua Zhang Zhuan Fu Junyao Gong Zhaozixuan Zhou Liangjun Xia State Key Laboratory of New Textile Materials and Advanced Processing Technologies Wuhan Textile UniversityWuhan 430200China College of Textiles Donghua UniversityShanghai 201620China School of Fashion and Textiles The Hong Kong Polytechnic UniversityHong Kong 999077China

Semiconductor heterojunction engineering and three-dimensional(3D)architecture con-struction have been considered highly desirable strategies to enhance photocatalytic ***,a BiOI/ZnO composite photocatalyst with a 3D flower-like architecture was successfully prepared,whichwas stably immobilized on three-dimensional porous lignocel-lulosic biomass Juncus effusus(JE)*** outstanding photocatalytic performance of the BiOI/ZnO-JE fiber was confirmed by the degradation of tetracycline hydrochloride(TC,90%),ciprofloxacin(CIP,79%),and norfloxacin(NOR,81%).The enhanced photocatalytic activities were mainly attributed to the synergistic absorption performance of the lignocellulosic JE and the effective transfer and separation of ***,the hydroxyl(·OH)and super-oxide radicals(·O_(2)^(−))are themain reactive species in the photocatalytic process according to the *** work may provide a novel perspective for constructing high-performance lignocellulosic-based photocatalytic materials.

关键词： Heterojunction BiOI/ZnO Organic pollutants Biomass-based Juncus effusus fiber Photodegradation

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Unraveling the impacts of intermolecular interaction on morphology evolution for highly efficient organic solar cells and modules

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Science China Chemistry 2025年第1期68卷 264-272页

作者： Xueqing Ma Yingying Cheng Yuqiang Liu Xinming Zheng Guangliu Ran Hongxiang Li Xinyue Cui Andong Zhang Wenkai Zhang Pei Cheng Wenchao Huang Zhishan Bo Beijing Key Laboratory of Energy Conversion and Storage Materials College of ChemistryBeijing Normal UniversityBeijing 100875China College of Textiles and Clothing State Key Laboratory of Bio-fibers and Eco-textilesQingdao UniversityQingdao 266071China Key State Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China Department of Physics and Applied Optics Beijing Area Major Laboratory Center for Advanced Quantum StudiesBeijing Normal UniversityBeijing 100875China State Key Laboratory of Polymer Materials Engineering College of Polymer Science and EngineeringSichuan UniversityChengdu 610065China

Understanding the effect of intermolecular interaction on the growth dynamic of active layers is critical for advancing organic solar cells(OSCs).However,the diverse structure of donors and acceptors makes the research *** with customizable structures and properties could simplify this ***,we meticulously tailor two additives of 3,4-ethylenedioxythiophene(EDOT)and 2,5-dibromo-3,4-ethylenedioxythiophene(DBEDOT),possessing distinct intermolecular interaction features to elaborate the inherent *** is found that varied interaction strengths can alter film formation *** enhanced intermolecular interaction between the DBEDOT and non-fullerene acceptor BTP-e C9-4F results in pre-aggregation and longer crystallization duration of BTP-e C9-4F,facilitating the formation of films with compact molecular packing and decent phase ***,exciton dissociation and charge transport become more ***,devices processed with DBEDOT exhibit a remarkable power conversion efficiency of 19.35%in small-area OSCs and 14.11%in bladecoated 5 cm×5 cm organic solar ***,OSCs can maintain 80%of their initial efficiency after continuous annealing at 85℃for over 2,100 h.

关键词： organic solar cell non-fullerene acceptor film growth molecular packing intermolecular interaction

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Facile and effective synthesis strategy for terbium-doped hydroxyapatite toward photoelectric devices and flexible functional fibers

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Rare Metals 2024年第4期43卷 1713-1723页

作者： Xiao-Dong Zhang Kun Nie Zi-Yao Hu Ran-Ran Zhou Xiu-Qiang Duan Wu-Bin Dai Song-Song Nie Song-Jun Yao Luo-Xin Wang Le-Fu Mei Hua Wang Yi-Yi Yao Xiao-Xue Ma Hubei Key Laboratory for New Textile Materials and Applications and State Key Laboratory of New Textile Materials and Advanced Processing Technology School of Materials Science and EngineeringWuhan Textile UniversityWuhan430200China Key Laboratory of Testing and Tracing of Rare Earth Products for State Market Regulation Jiangxi University of Science and TechnologyGanzhou341000China Hubei Key Laboratory of Plasma Chemistry and Advanced Materials and Key Laboratory of Green Chemical Engineering Process of Ministry of Education Wuhan Institute of TechnologyWuhan430205China

As a material with good biocompatibility,hydroxyapatite(HAP)can have optical properties after doping with various rare earth *** a biocompatible fluorescent material,doped HAP could have broad applications in biological probes,drug delivery,optoelectronic materials,fluorescence anti-counterfeiting,and other *** this paper,we put forward the preparation of HAP doped with terbium(Ⅲ)ions(Tb^(3+))by hydrothermal *** controlling the Tb^(3+)doping content in reaction and the reaction time,the changes in HAP's structure,morphology,and luminescence properties under different conditions were *** the doping amount of Tb^(3+)reached an optimal value,the dipole-quadrupole would occur and the concentration would be *** control experiment showed that the optimal Tb3+content was 7.5×10^(-5)mol,which showed the best fluorescence ***,a non-luminous material,was rarely used in the field of fluorescent anti-counterfeiting and photoelectric *** proposed to prepare a luminescent aramid/polyphenylene sulfide(ACFs/PPS)fiber paper and a new light-emitting diode(LED)using the Tb-doped HAP *** composite sample exhibited an excellent stability and fluorescence performance,which also demonstrated a possibility of HAP applications in anticounterfeiting and *** introduction of Tb3+dopant HAP was done to give HAP optical properties and broaden the application range of HAP.

关键词： Hydroxyapatite Rare earth luminescence Photoelectric device Aramid Polyphenylene sulfide fiber paper Luminescent fiber

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Homologous CoS2 interface with directed electron transfer and strong chloridion repulsion for efficient seawater oxidation

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Science China Chemistry 2025年第5期68卷 1869-1878页

作者： Yuan Tian Jiang-Bo Chen Jie Ying Ge Tian Yu-Xuan Xiao Yi Lu Si-Ming Wu Wei Geng Ling Shen Xiao-Yu Yang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and School of Materials Science and Engineeringand Shenzhen Research Institute & Laoshan LaboratoryWuhan University of Technology School of Chemical Engineering and Technology Sun Yat-sen University National Energy Key Laboratory for New Hydrogen-Ammonia Energy Technologies Foshan Xianhu Laboratory

Seawater electrolysis is a highly promising method to produce high energy density hydrogen,especially in dry areas that have scarce freshwater ***,application of seawater electrolysis is confronted by two major problems associated with catalysts employed for the anodic oxygen evolution reaction（OER） including the competitive hypochlorite evolution reaction（HCER） and strong chloridion（Cl-） triggered *** studies aimed at overcoming these problems,a facile method has been developed to synthesize a homologous CoS2heterojunction as an OER *** to a difference in work functions at the interface and increased electron density,this material has directed electron transfer and strong chloridion repulsion properties,*** have shown that CoS2achieves low overpotentials of 289 and 322 mV at 10 mA cm-2current density in respective alkaline（1 M KOH） and alkaline simulated seawater ***,the outstanding stability of CoS2is reflected in a negligible decline in activity during promotion of the OER for 100 *** of density functional theory calculations reveal that the homologous CoS2heterojunction promotes directed electron transport for optimizing adsorption/desorption of reactive species and heightens the Cl-adsorption energy for strongly repulsing Cl-,phenomena that enhance OER performance in alkaline simulated seawater.

关键词： metal sulfide homologous heterojunction directed transfer chloride ion repulsion seawater electrolysis

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Chiral electrolytes for rechargeable metal batteries

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Journal of Energy Chemistry 2025年第3期102卷 834-841页

作者： Lan-Qing Wu Yu-Jie Ning Zhen-Yu Fan Zhe Li Kun Li Jia Li Shuang-Xin Ren Dubin Huang Yang Yang Weiwei Xie Huan Wang Qing Zhao Frontiers Science Center for New Organic Matter Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education)State Key Laboratory of Advanced Chemical Power SourcesCollege of ChemistryNankai UniversityTianjin 300071China Beijing Golden Feather New Energy Technology Co. LtdBeijing 100080China

Charge transfer at the liquid(electrolyte)-solid(metal)interfaces is of fundamental importance to metal electrochemical deposition that further determines the reversibility and kinetics of energy-dense rechargeable metal batteries(RMBs).We demonstrate the fast charge transfer at the electrolyte-metal interfaces for lithium metal by designing and synthesizing electrolytes with chiral solvents:R(or S)-1,2-dimethoxy pro pane(R-DMP or S-DMP)and R(or S)-4-methyl-1,3-dioxolane(R-MDOL or S-MDOL).The chiral-induced spin selectivity is considered to produce spin-polarized metal surfaces,enabling the improvement in charge transfer rate and *** deposited Li metal in chiral electrolytes shows smooth and uniform morphologies,as well as high initial(>95%)and average(~99.2%)Coulombic efficiency for Li metal stripping/plating process,thus prolonging the life-span of batteries using thin lithium anode(50μm)to 400 cycles till 80%capacity *** work provides a distinct approach to regulate metal deposition beyond the limitation of ion de-solvation.

关键词： Chiral ether electrolytes Electrode kinetics Li metal batteries Metal deposition Solvation structures

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Photoexcitation-induced passivation of SnO2 thin film for efficient perovskite solar cells

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National Science Review 2023年第11期10卷 183-191页

作者： Nianyao Chai Xiangyu Chen Zhongle Zeng Ruohan Yu Yunfan Yue Bo Mai Jinsong Wu Liqiang Mai Yi-Bing Cheng Xuewen Wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of Technology National Energy Key Laboratory for New Hydrogen-Ammonia Energy Technologies Foshan Xianhu Laboratory

A high-quality tin oxide electron transport layer(ETL) is a key common factor to achieve high-performance perovskite solar cells(PSCs). However, the conventional annealing technique to prepare high-quality ETLs by continuous heating under near-equilibrium conditions requires high temperatures and a long fabrication time. Alternatively, we present a non-equilibrium, photoexcitation-induced passivation technique that uses multiple ultrashort laser pulses. The ultrafast photoexcitation and following electron–electron and electron–phonon scattering processes induce ultrafast annealing to efficiently passivate surface and bulk defects, and improve the crystallinity of Sn O2, resulting in suppressing the carrier recombination and facilitating the charge transport between the ETL and perovskite interface. By rapidly scanning the laser beam, the annealing time is reduced to several minutes, which is much more efficient compared with conventional thermal annealing. To demonstrate the university and scalability of this technique, typical antisolvent and antisolvent-free processed hybrid organic–inorganic metal halide PSCs have been fabricated and achieved the power conversion efficiency(PCE) of 24.14% and 22.75% respectively, and a12-square-centimeter module antisolvent-free processed perovskite solar module achieves a PCE of 20.26%,with significantly enhanced performance both in PCE and stability. This study establishes a new approach towards the commercialization of efficient low-temperature manufacturing of PSCs.

关键词： photoexcitation-induced passivation ultrafast laser carrier management electron transport layer perovskite solar cells

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High-strength,electrically insulated industrial meta-aramid paper reinforced with polyethylene terephthalate microfibre pulp in a sandwich structure

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High Voltage 2024年第6期9卷 1402-1413页

作者： Meijun Chen Songjun Yao Guobin Zhu Mengyun Wu Zhiying Li Siwei Xiong Shiwen Yang Hua Wang Liangbo Zhu Luoxin Wang State Key Laboratory of New Textile Materials&Advanced Processing Technology College of Materials Science and EngineeringWuhan Textile UniversityWuhanChina High-Tech Organic Fibers Key Laboratory of Sichuan Province ChengduSichuanChina

The weak interfacial strength and porous structure of the meso-aramid paper cause mechanical and insulating *** density,regulating pore structure,and improving interfacial interactions of meso-aramid are crucial for promoting the perfor-mance of meso-aramid papers.A PMIA/polyethylene terephthalate(PET)composite paper was prepared using the wet method with meso-aramid short cut fibres(PMIA)and PET pulp as raw *** sandwich-structured PMIA/PET paper was achieved by covering PET microfiber non-wovens served as the surface layer while the PMIA/PET composite paper acted as the core *** the high-temperature hot pressing process,the PET pulp transformed into a viscous melt that coated on aramid fibres in between layers,forming a typical‘reinforced concrete’interface structure within the core layer of the PMIA/PET composite *** PET non-wovens on top and bottom surfaces were converted into a dense PET film that filled and covered the holes and defects in the PMIA/PET composite *** unique structure enabled the sandwich-structured PMIA/PET composite paper to exhibit excellent tensile strength(80.41 N/cm)and breakdown strength(56.35 kV/mm),surpassing most reported performances of meso-aramid papers in *** work not only provides novel insights for pre-paring high-performance meso-aramid papers,but also shows potential applications for other materials and structures.

关键词： strength structure sandwich

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