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NiFeRuO_(x)nanosheets on Ni foam as an electrocatalyst for efficient overall alkaline seawater splitting

Frontiers of Chemical Science and Engineering 2023年第11期17卷 1698-1706页

作者： Yu Liu Lin Chen Yong Wang Yuan Dong Liang Zhou Susana ICórdoba de Torresi Kenneth IOzoemena Xiao-Yu Yang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing&International School of Materials Science and Engineering&School of Materials Science and Engineering&Shenzhen Research Institute&Laoshan Laboratory Wuhan University of TechnologyWuhan 430070China Instituto de Química Universidade de São Paulo05508-080 São PauloBrazil Molecular Sciences Institute School of ChemistryUniversity of the WitwatersrandJohannesburg 2050South Africa

The electrocatalyst NiFeRuO_(x)/NF,comprised of NiFeRuO_(x)nanosheets grown on Ni foam,was synthesized using a hydrothermal process followed by thermal ***_(x)/NF displays high electrocatalytic activity and stability for overall alkaline seawater splitting:98 mV@10 mA∙cm^(−2)in hydrogen evolution reaction,318 mV@50 mA∙cm^(−2)in oxygen evolution reaction,and a cell voltage of 1.53 V@10 mA∙cm^(−2),as well as 20 h of durability.A solar-driven system containing such a bifunctional NiFeRuO_(x)/NF has an almost 100%Faradaic *** NiFeRuO_(x)coating around Ni foam is an anti-corrosion layer and also a critical factor for enhancement of bifunctional performances.

关键词： NiFeRuO_(x)nanosheets Ni foam electrocatalysis overall seawater splitting solar-driven system

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Threee-dimensionally ordered macroporous materials for pollutants abatement,environmental sensing and bacterial inactivation

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中国科学：化学（英文版） 2023年第7期66卷 1886-1904页

作者： Yang Ding Chun-Hua Wang Jia-Song Zhong Qi-Nan Mao Run-Tian Zheng Yun Hau Ng Ming-Hui Sun Soumyajit Maitra Li-Hua Chen Bao-Lian Su Center of Advanced Optoelectronic Materials College of Materials and Environmental EngineeringHangzhou Dianzi UniversityHangzhou 310018China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium School of Energy and Environment City University of Hong KongHong Kong 999000China Center of Advanced Optoelectronic Materials College of Materials and Environmental EngineeringHangzhou Dianzi UniversityHangzhou 310018China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Materials University of OxfordOxford OX1 3PHUK Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Clare Hall University of CambridgeCambridge CB2 1EWUK

Owing to their facile reactants migration channels,large surface area,maximized exposure of reaction sites and efficient light utilization,three-dimensionally ordered macroporous(3DOM)materials have been extensively adopted in environmental fields such as pollutants removal,environmental detection as well as bacterial *** this review,the up-to-date 3DOM materials,the corresponding synthesis protocols and the related environmental applications involving photo/electrocatalytic pollutants decomposition,thermocatalytic volatile organic compounds(VOCs)elimination,hazardous substances sensing and bacteria inactivation are completely ***,the inherent advantages and mechanisms of 3DOM materials in different environmental utilization are thoroughly demonstrated and ***,the improved performance of environmental applications and the methods of fabricating 3DOM materials are correlated in depth,being favorable for readers to obtain the fundamental knowledge and to motivate some innovative thoughts for modifying 3DOM materials with further elevated environmental remediation ***,the current difficulties and prospects of 3DOM materials for large-scale and commercial applications are *** critical review is anticipated to promote the optimization of 3DOM materials and to ripen the related environmental remediation techniques.

关键词： 3DOM environmental remediation catalysis VOCs disinfection

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Self-assembled monolayers(SAMs)in inverted perovskite solar cells and their tandem photovoltaics application

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Interdisciplinary materials 2024年第2期3卷 203-244页

作者： Zijun Yi Xin Li Yuchen Xiong Guibin Shen Wenguang Zhang Yihuai Huang Qinghui Jiang Xin Ren Ng Yubo Luo Jianghui Zheng Wei Lin Leong Fan Fu Tongle Bu Junyou Yang State Key Laboratory of Material Processing and Die&Mould Technology Huazhong University of Science and TechnologyWuhanChina China‐Eu Institute for Clean and Renewable Energy Huazhong University of Science and TechnologyWuhanChina School of Electrical and Electronic Engineering Nanyang Technological UniversitySingaporeSingapore Department of Chemistry National University of SingaporeSingaporeSingapore School of Physics The University of SydneySydneyNew South WalesAustralia Laboratory for Thin Films and Photovoltaics Empa‐Swiss Federal Laboratories for Materials Science and TechnologyDübendorfSwitzerland State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhanChina

Self-assembled monolayers(SAMs)employed in inverted perovskite solar cells(PSCs)have achieved groundbreaking progress in device efficiency and stability for both single-junction and tandem configurations,owing to their distinctive and versatile ability to manipulate chemical and physical interface *** this regard,we present a comprehensive review of recent research advancements concerning SAMs in inverted perovskite singlejunction and tandem solar cells,where the prevailing challenges and future development prospects in the applications of SAMs are *** thoroughly examine the mechanistic roles of diverse SAMs in energy-level regulation,interface modification,defect passivation,and charge *** is achieved by understanding how interfacial molecular interactions can be finely tuned to mitigate charge recombination losses in inverted *** this comprehensive review,we aim to provide valuable insights and references for further investigation and utilization of SAMs in inverted perovskite single‐junction and tandem solar cells.

关键词： inverted perovskite solar cells power conversion efficiency self-assembled monolayers tandem

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Sodium vanadium oxides:From nanostructured design to high-performance energy storage materials

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Journal of materials Science & technology 2022年第26期121卷 80-92页

作者： Yifan Dong Shuolei Deng Ziting Ma Ge Yin Changgang Li Xunlong Yuan Huiyun Tan Jing Pan Liqiang Mai Fan Xia Engineering Research Center of Nano-Geomaterials of Ministry of Education Faculty of Material Science and ChemistryChina University of GeosciencesWuhan 430074China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan 430070China

Developing high-capacity and low-cost cathode materials for metal-ion rechargeable batteries is the mainstream trend and is also the key to providing breakthroughs in making high-energy rechargeable *** has a variety of valence states and can form a variety of vanadate *** a typical positive electrode material,vanadate has abundant ion adsorption sites,a unique“pillar”framework,and a typical layered ***,it has the advantages of high specific capacity and excellent rate performance,possessing the prospect of being a large-capacity energy storage *** this review,we focus on applications of sodium vanadium oxides(NVO)in electrical energy storage(EES)devices and summarize sodium vanadate materials from three aspects,including crystal structure,electrochemical performance,and energy storage *** recent progress of NVO-based highperformance energy storage materials along with nanostructured design strategies was provided and discussed as *** review is intended to serve as general guidance for researchers to develop desirable sodium vanadate materials.

关键词： Sodium vanadate Nanostructured materials Rechargeable metal-ion batteries Energy storage mechanism

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Boosting Li-ion storage in Li2MnO_(3) by unequal-valent Ti4+-substitution and interlayer Li vacancies building

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Chinese Chemical Letters 2023年第4期34卷 564-569页

作者： Yu Tian Yuling Zhao Fanqi Meng Kaicheng Zhang Yanyuan Qi Yujie Zeng Congcong Cai Yuli Xiong Zelang Jian Yang Sun Lin Gu Wen Chena School of Materials Science and Engineering Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Materials Shenzhen Campus of Sun Yat-sen UniversityShenzhen 518107China C Innovation Laboratory Contemporary Amperex Technology Ltd.(CATL)Ningde 352100China Institute of Physics Chinese Academy of SciencesBeijing 100190China Sanya Science and Education Innovation Park of Wuhan University of Technology Wuhan 430070China

Lithium rich layered oxide(LRLO) has been considered as one of the promising cathodes for lithium-ion batteries(LIBs). The high voltage and large capacity of LRLO depend on Li2MnO_(3)phase. To ameliorate the electrochemical performance of Li2MnO_(3), also written as Li(Li1/3Mn2/3)O_(2), we propose a strategy to substitute Mn4+and Li+in Mn/Li transition metal layer with Ti4+, which can stabilize the structure of Li2MnO_(3)by inhibiting the excessive oxidation of O_(2)-above 4.5 V. More significantly, the unequal-valent substitution brings about the emergence of interlayer Li vacancies, which can promote the Li-ion diffusion based on the enlarged interlayer and increase the capacity by activating the Mn3+/4+redox. We designed Li0.7[Li1/3Mn2/3]0.7Ti0.3O_(2)with high interlayer Li vacancies, which presents a high capacity(290 m Ah/g at 10 m A/g) and stable cycling performance(84% over 60 cycles at 50 m A/g). We predict that this strategy will be helpful to further improve the electrochemical performance of LRLOs.

关键词： Lithium-ion batteries Li2MnO_(3) Unequal-valent Ti4+-substitution Interlayer Li vacancies Activated Mn3+/4+redox

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Uniform Metal Sulfide@N-doped Carbon Nanospheres for Sodium Storage: Universal synthesis Strategy and Superior Performance

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Energy & Environmental materials 2023年第2期6卷 389-396页

作者： Kai Yang Hao Fu Yixue Duan Manxiang Wang Minh Xuan Tran Joong Kee Lee Woochul Yang Guicheng Liu Department of Physics Dongguk UniversitySeoul 04620Korea Shaanxi Key Laboratory of Chemical Additives for Industry Shaanxi University of Science and TechnologyXi’an 710021China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China College of Physics and Electronic Information Yan’an UniversityYan’an 716000China Center for Energy Storage Research Clean Energy InstituteKorea Institute of Science and Technology(KIST)Seoul 02792Korea

Nitrogen-doped carbon-coated transition-metal sulfides(TMS@NCs)have been considered as efficient anodes for sodium-ion ***,the uncontrollable morphology and weak core-shell binding forces significantly limit the sodium storage performance and ***,based on the reversible ring-opening reaction of the epoxy group of the tertiary amino group-rich epoxide cationic polyacrylamide(ECP)at the beginning of hydrothermal process(acidic environment)and the irreversible ring-opening(cross-linking reactions)at the late hydrothermal period(alkaline environment),47 nm-sized ZnS@NCs were prepared via a one-pot hydrothermal *** this process,the covalent bonds formed between the ZnS core and elastic carbon shell significantly improved the mechanical and chemical stabilities of ZnS@*** from the nanosize,fast ion/electron transfer,and high stability,ZnS@NC exhibited a high reversible capacity of 421.9 mAh g^(−1) at a current density of 0.1 A g^(−1) after 1000 cycles and a superior rate capability of 273.8 mAh g^(−1) at a current density of 5 A g^(−1).Moreover,via this universal synthesis strategy,a series of TMS@NCs,such as MoS_(2)@NC,NiS@NC,and CuS@NC were developed with excellent capacity and cyclability.

关键词： anode materials core-shell structure nitrogen-doped carbon ring-opening reaction transition-metal sulfide

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Engineering surface framework TiO6 single sites for unprecedented deep oxidative desulfurization

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National Science Review 2024年第5期11卷 303-314页

作者： Shen Yu Zhan Liu Jia-Min Lyu Chun-Mu Guo Xiao-Yu Yang Peng Jiang Yi-Long Wang Zhi-Yi Hu Ming-Hui Sun Yu Li Li-Hua Chen Bao-Lian Su Laboratory of Living Materials at the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Nanostructure Research Center Wuhan University of Technology School of Chemistry Chemical Engineering and Life ScienceWuhan University of Technology Laboratory of Inorganic Materials Chemistry University of Namur

Catalytic oxidative desulfurization（ODS） using titanium silicate catalysts has emerged as an efficient technique for the complete removal of organosulfur compounds from automotive fuels. However, the precise control of highly accessible and stable-framework Ti active sites remains highly challenging. Here we reveal for the first time by using density functional theory calculations that framework hexa-coordinated Ti（TiO6） species of mesoporous titanium silicates are the most active sites for ODS and lead to a lower-energy pathway of ODS. A novel method to achieve highly accessible and homogeneously distributed framework TiO6active single sites at the mesoporous surface has been developed. Such surface framework TiO6species exhibit an exceptional ODS performance. A removal of 920 ppm of benzothiophene is achieved at60°C in 60 min, which is 1.67 times that of the best catalyst reported so far. For bulky molecules such as4,6-dimethyldibenzothiophene（DMDBT）, it takes only 3 min to remove 500 ppm of DMDBT at 60°C with our catalyst, which is five times faster than that with the current best catalyst. Such a catalyst can be easily upscaled and could be used for concrete industrial application in the ODS of bulky organosulfur compounds with minimized energy consumption and high reaction efficiency.

关键词： electrostatic interactions framework hexa-coordinated Ti site oxidative desulfurization mesoporous materials self-assembly

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Atomic Level Dispersed Metal–Nitrogen–Carbon Catalyst toward Oxygen Reduction Reaction: synthesis Strategies and Chemical Environmental Regulation

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Energy & Environmental materials 2021年第1期4卷 5-18页

作者： Hengbo Yin Huicong Xia Shuyan Zhao Kexie Li Jianan Zhang Shichun Mu College of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

For development and application of proton exchange membrane fuel cell(PEMFC) energy transformation technology, the cost performance must be elevated for the catalyst. At present, compared with noble metal-based catalysts, such as Pt-based catalysts, atomically dispersed metal–nitrogen–carbon(M–N–C) catalysts are popularity and show great potential in maximizing active site density, high atom utilization and high activity,making them the first choice to replace Pt-based catalysts. In the preparation of atomically dispersed metal–nitrogen–carbon catalyst, it is difficult to ensure that all active sites are uniformly dispersed, and the structure system of the active sites is not optimal. Based on this, we focus on various approaches for preparing M–N–C catalysts that are conducive to atomic dispersion, and the influence of the chemical environmental regulation of atoms on the catalytic sites in different catalysts. Therefore, we discuss the chemical environmental regulation of the catalytic sites by bimetals, atom clusters, and heteroatoms(B, S, and P). The active sites of M–N–C catalysts are explored in depth from the synthesis and characterization, reaction mechanisms, and density functional theory(DFT)calculations. Finally, the existing problems and development prospects of the current atomic dispersion M–N–C catalyst are proposed in detail.

关键词： atomic-level catalyst chemical environmental effects metal-nitrogen-carbon oxygen reduction reaction synthesis strategy

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Bioinspired urchin-like murray carbon nanostructure with protection shell for advanced lithium-sulfur batteries

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Journal of Energy Chemistry 2023年第10期85卷 1-10,I0002页

作者： Ya-Wen Tian Yong Yu Liang Wu Min Yan Wen-Da Dong Chen-Yang Wang Hemdan S.H.Mohamed Zhao Deng Li-Hua Chen Tawfique Hasan Yu Li Bao-Lian Su State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina School of Automotive Engineering Xiangyang PolytechnicXiangyang 441050HubeiChina Hubei Key Laboratory of Plasma Chemistry and Advanced Materials Hubei Engineering Technology Research Center of Optoelectronic and New Energy MaterialsSchool of Materials Science and EngineeringWuhan Institute of TechnologyWuhan 430205HubeiChina Physics Department Faculty of ScienceFayoum UniversityEl Gomhoria Street63514 FayoumEgypt Cambridge Graphene Centre University of CambridgeCambridge CB30FAUnited Kingdom Laboratory of Inorganic Materials Chemistry(CMI) University of Namur61 rue de BruxellesB-5000 NamurBelgium

Commercial application of lithium-sulfur(Li-S) batteries is hindered by the insulating nature of sulfur and the dissolution of polysulfides. Here, a bioinspired 3D urchin-like N-doped Murray's carbon nanostructure(N-MCN) with interconnected micro-meso-macroporous structure and a polydopamine protection shell has been designed as an effective sulfur host for high-performance Li-S batteries. The advanced 3D hierarchically porous framework with the characteristics of the generalized Murray's law largely improves electrolyte diffusion, facilitates electrons/ions transfer and provides strong chemisorption for active species, leading to the synergistic structural and chemical confinement of polysulfides. As a result,the obtained P@S/N-MCN electrode with high areal sulfur loading demonstrates high capacity at high current densities after long cycles. This work reveals that following the generalized Murray's law is feasible to design high-performance sulfur cathode materials for potentially practical Li-S battery applications.

关键词： Li-S batteries Murray’s law Hierarchically porous framework N-doped carbon Structural-chemical confinement

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Bioactive calcium and mangnesium phosphate bone adhesive for enhanced vascularization and bone regeneration

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Journal of materials Science & technology 2023年第33期164卷 246-257页

作者： Jiawei Liu Honglei Kang Wenying Wei Rong Tu Takashi Goto Feng Li Honglian Dai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Biomedical Materials and Engineering Research Center of Hubei ProvinceWuhan University of TechnologyWuhan 430070China Department of Orthopedics Tongji HospitalTongji Medical CollegeHuazhong University of Science and TechnologyWuhan 430030China Chaozhou Branch of Chemistry and Chemical Engineering Guangdong Laboratory Chaozhou 521000China New Industry Creation Hatchery Center Tohoku UniversitySendai 980-8579Japan

Bone adhesive is a promising material for the treatment of bone fractures,which is helpful for the fast and effective reduction and fixation of broken ***,the existing adhesives bond weakly to bone tissues,and are non-absorbable,or hard to cure under wet ***,inspired by the cement-based adhesive used in the industry field,we report a bioactive calcium and magnesium phosphate bone adhesive(MPBA)with the properties of facile preparation,robust adhesion,and *** is equipped with similar strength to cancellous bones and shows reliable bonding performance for various interfaces,such as Ti6Al4V,Al2O3,and poly(ether-ether-ketone).MPBA achieves excellent bonding ability for the above interfaces with the bonding strengths of 2.28±0.47,2.32±0.15,and 1.44±0.38 MPa,***,it also shows reliable fixation ability for bovine bone *** bonding behavior to materials and bones suggests that MPBA could be used for both fracture treatment and implant ***,MPBA possesses good biological activity,which could promote the vascularization process and osteogenic ***,in vivo experiments confirmed MPBA can effectively restore bone strength and promote bone regeneration.

关键词： Fracture Calcium magnesium phosphate cement Bone adhesives

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