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Energy Storage: Porous One‐Dimensional Nanomaterials: Design, Fabrication and Applications in Electrochemical Energy Storage (Adv. Mater. 20/2017)

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advanced materials 2017年第20期29卷

作者： Qiulong Wei Fangyu Xiong Shuangshuang Tan Lei Huang Esther H. Lan Bruce Dunn Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and Engineering Wuhan 430070 P. R. China Department of Materials Science and Engineering University of California Los Angeles Los Angeles CA 90095–1595 USA

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A Ternary Solvent Method for Large‐Sized Two‐Dimensional Perovskites

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Angewandte Chemie 2017年第9期129卷

作者： Junnian Chen Lin Gan Fuwei Zhuge Huiqiao Li Jizhong Song Haibo Zeng Tianyou Zhai State Key Laboratory of Material Processing and Die & Mould Technology School of Materials Science and Engineering Huazhong University of Science and Technology Wuhan 430074 P.R. China MIIT Key Laboratory of Advanced Display Materials and Devices Institute of Optoelectronics & Nanomaterials College of Materials Science and Engineering Nanjing University of Science and Technology Nanjing 210094 P.R. China

Recent reports demonstrate that a two‐dimensional (2D) structural characteristic can endow perovskites with both remarkable photoelectric conversion efficiency and high stability, but the synthesis of ultrathin 2D perovskites with large sizes by facile solution methods is still a challenge. Reported herein is the controlled growth of 2D (C 4 H 9 NH 3 ) 2 PbBr 4 perovskites by a chlorobenzene‐dimethylformide‐acetonitrile ternary solvent method. The critical factors, including solvent volume ratio, crystallization temperature, and solvent polarity on the growth dynamics were systematically studied. Under optimum reaction condition, 2D (C 4 H 9 NH 3 ) 2 PbBr 4 perovskites, with the largest lateral dimension of up to 40 μm and smallest thickness down to a few nanometers, were fabricated. Furthermore, various iodine doped 2D (C 4 H 9 NH 3 ) 2 PbBr x I 4− x perovskites were accessed to tune the optical properties rationally.

关键词： Kristallwachstum Oberflächenchemie Perowskite Synthesemethoden Ternäre Lösungsmittel

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Perovskite Solar Cells: Solvent‐Mediated Dimension Tuning of Semiconducting Oxide Nanostructures as Efficient Charge Extraction Thin Films for Perovskite Solar Cells with Efficiency Exceeding 16% (Adv. Energy Mater. 7/2016)

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advanced Energy materials 2016年第7期6卷

作者： Wu‐Qiang Wu Fuzhi Huang Dehong Chen Yi‐Bing Cheng Rachel A. Caruso Particulate Fluids Processing Centre School of Chemistry The University of Melbourne Melbourne VIC 3010 Australia State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Department of Materials Science and Engineering Monash University VIC 3800 Australia CSIRO Manufacturing Private Bag 10 Clayton South VIC 3169 Australia

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Ammonium Ion Batteries: material, Electrochemistry and Strategy

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Angewandte Chemie (International ed. in English) 2023年第23期62卷 e202301629页

作者： Runtian Zheng Yuhang Li Haoxiang Yu Xikun Zhang Ding Yang Lei Yan Yu Li Jie Shu Bao-Lian Su School of Materials Science and Chemical Engineering Ningbo University Ningbo 315211 Zhejiang China. Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 rue de Bruxelles 5000 Namur Belgium. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 Hubei China.

Ammonium-ion batteries (AIBs) have recently attracted increasing attention in the field of aqueous batteries owing to their high safety and fast diffusion kinetics. The NH storage mechanism is quite different from that of spherical metal ions (e.g. Li , Na , K , Mg , and Zn ) because of the formation of hydrogen bonds between NH and host materials. Although many materials have been proposed as electrode materials for AIBs, their performances hardly meet the requirement of future electrochemical energy storage devices. It is thus urgent to design and exploit advanced materials for AIBs. This review highlights the state-of-the-art research on AIBs. The insights into the basic configuration, operating mechanism and recent progress of electrode materials and corresponding electrolytes for AIBs have been comprehensively outlined. The electrode materials are classified and compared according to different NH storage behaviour in the structure. The challenges, design strategies and perspectives are also discussed for the future development of AIBs.

关键词： Ammonium-Ion Batteries Aqueous Electrolytes Electrode materials Hydrogen Bond Operating Mechanisms

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Carbon Nanocage Supported Asymmetrically Coordinated Nickle Single-Atom for Enhanced CO2Electroreduction in Membrane Electrode Assembly

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Angewandte Chemie 2024年第2期137卷

作者： Yingxi Lin Chenfeng Xia Zhaozhao Zhu Junjie Wang Huiting Niu Shuning Gong Zhao Li Na Yang Prof. Jun Song Chen Dr. Rui Wu Bao Yu Xia School of Materials and Energy University of Electronic Science and Technology of China Chengdu 610054 China School of Chemistry and Chemical Engineering State Key Laboratory of Materials Processing and Die & Mould Technology Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure Wuhan National Laboratory for Optoelectronics Huazhong University of Science and Technology (HUST) 1037 Luoyu Road Wuhan 430074 China Interdisciplinary Materials Research Center Institute for Advanced Study Chengdu University Chengdu 610106 China

Designing efficient catalysts for operating CO 2 electroreduction in membrane electrode assembly (MEA) faces significant obstacles. Herein, we propose an asymmetrically coordinated Ni single-atom catalyst featuring axial Br coordination at NiN 4 Br sites anchoring onto hollow Br/N co-doped carbon nanocages, achieved through a NaBr-assisted confined-pyrolysis strategy. The Ni-NBr-C catalyst exhibits a high CO Faradaic efficiency (FE CO >97 %) over the current density range of 50 to 350 mA cm −2 in the MEA device. Furthermore, Ni-NBr-C shows a stable cell voltage of 2.66±0.2 V while delivering a large current density of 350 mA cm −2 over an 85-hour long-term operation, demonstrating its potential for industrial-scale applications. advanced characterization techniques and theoretical calculations reveal that the coordination and doping of Br not only enhance the intrinsic activity but also highlight that the unique pore structure improves mass transfer efficiency.

关键词： CO2 electroreduction Membrane electrode assembly Carbon nanocages Single atom Asymmetrical coordination

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Confining Conversion Chemistry in Intercalation Host for Aqueous Batteries

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Angewandte Chemie 2024年第38期136卷

作者： Qiuyue Gui Wenjun Cui Deliang Ba Prof. Xiahan Sang Prof. Yuanyuan Li Jinping Liu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology Wuhan Hubei 430070 China Nanostructure Research Center Wuhan University of Technology Wuhan Hubei 430070 China School of Integrated Circuits Huazhong University of Science and Technology Wuhan Hubei 430074 China

Conversion-type anode materials with high theoretical capacities play a pivotal role in developing future aqueous rechargeable batteries (ARBs). However, their sustainable applications have long been impeded by the poor cycling stability and sluggish redox kinetics. Here we show that confining conversion chemistry in intercalation host could overcome the above challenges. Using sodium titanates as a model intercalation host, an integrated layered anode material of iron oxide hydroxide-pillared titanate (FeNTO) is demonstrated. The conversion reaction is spatially and kinetically confined within sub-nano interlayer, enabling superlow redox polarization (ca. 4–6 times reduced), ultralong lifespan (up to 8700 cycles) and excellent rate performance. Notably, the charge compensation of interlayer via universal cation intercalation into host endows FeNTO with the capability of operating well in a broad range of aqueous electrolytes (Li + , Na + , K + , Mg 2+ , Ca 2+ , etc.). We further demonstrate the large-scale synthesis of FeNTO thin film and powder, and rational design of quasi-solid-state high-voltage ARB pouch cells powering wearable electronics against extreme mechanical abuse. This work demonstrates a powerful confinement means to access disruptive electrode materials for next-generation energy devices.

关键词： conversion chemistry intercalation host sub-nano confinement aqueous rechargeable batteries wearable pouch cell

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Annealing effects on structure and mechanical properties of CoCrFeNiTiAlx high-entropy alloys

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IOP Conference Series: materials Science and Engineering 2011年第1期20卷

作者： K B Zhang Z Y Fu J Y Zhang W M Wang S W Lee K Niihara State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Department of Materials Engineering SunMoon University Asan ChungNam 336-708 South Korea Extreme Energy-Density Research Institute Nagaoka University of Technology 1603-1 Nagaoka Niigata 940-2188 Japan

Novel CoCrFeNiTiAlx(x:molar ratio, other elements are equimolar) high-entropy alloys were prepared by vacuum arc melting and these alloys were subsequently annealed at 1000 °C for 2 h. The annealing effects on structure and mechanical properties were investigated. Compared with the as-cast alloys, there are many complex intermetallic phases precipitated from the solid solution matrix in the as-annealed alloys with Al content lower than Al1.0. Only simple BCC solid solution structure appears in the as-annealed Al1.5 and Al2.0 alloys. This kind of alloys exhibit high resistance to anneal softening. Most as-annealed alloys possess even higher Visker hardness than the as-cast ones. The as-annealed Al0.5 alloys shows the highest compressive strength while the Al0 alloy exhibits the best ductility, which is about 2.6 GPa and 13%, respectively. The CoCrFeNiTiAlx high-entropy alloys possess integrated high temperature mechanical property as well.

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Regulated High-Spin state and Constrained Charge Behavior of Active Cobalt Sites in Covalent Organic Frameworks for Promoting Electrocatalytic Oxygen Reduction

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Angewandte Chemie 2023年第27期135卷

作者： Zhi-yuan Mei Genfu Zhao Chenfeng Xia Sheng Cai Qi Jing Xuelin Sheng Han Wang Xiaoxiao Zou Lilian Wang Prof. Hong Guo Prof. Bao Yu Xia International Joint Research Center for Advanced Energy Materials of Yunnan Province Yunnan Key Laboratory of Carbon Neutrality and Green Low-carbon Technologies School of Materials and Energy Yunnan University 650091 Kunming China Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure State Key Laboratory of Materials Processing and Die & Mould Technology School of Chemistry and Chemical Engineering Huazhong University of Science and Technology (HUST) 1037 Luoyu Road 430074 Wuhan China

A novel type of covalent organic frameworks has been developed by assembling definite cobalt-nitrogen-carbon configurations onto carbon nanotubes using linkers that have varying electronic effects. This innovative approach has resulted in an efficient electrocatalyst for oxygen reduction, which is understood by a combination of in situ spectroelectrochemistry and the bond order theorem. The strong interaction between the electron-donating carbon nanotubes and the electron-accepting linker mitigates the trend of charge loss at cobalt sites, while inducing the generation of high spin state. This enhances the adsorption strength and electron transfer between the cobalt center and reactants/intermediates, leading to an improved oxygen reduction capability. This work not only presents an effective strategy for developing efficient non-noble metal electrocatalysts through reticular chemistry, but also provides valuable insights into regulating the electronic configuration and charge behavior of active sites in designing high-performance electrocatalysts.

关键词： Covalent Organic Framework Electrocatalyst Molecule Oxygen Reduction Spin state

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Applications of hierarchically structured porous materials from energy storage and conversion, catalysis, photocatalysis, adsorption, separation, and sensing to biomedicine

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Chemical Society reviews 2016年第12期45卷 3479-563页

作者： Ming-Hui Sun Shao-Zhuan Huang Li-Hua Chen Yu Li Xiao-Yu Yang Zhong-Yong Yuan Bao-Lian Su State Key Laboratory of Advanced Technology for Material Synthesis and Processing Wuhan University of Technology Luoshi Road 122 Wuhan 430070 China. chenlihua@*** baoliansu@***. Collaborat Innovat. Ctr. Chem. Sci. & Engn. Tianjin Key Lab. Adv. Energy Mat. Chem. Minist. Educ. Coll. Chem. Nankai Univ. Tianjin 300071 China. State Key Laboratory of Advanced Technology for Material Synthesis and Processing Wuhan University of Technology Luoshi Road 122 Wuhan 430070 China. chenlihua@*** baoliansu@*** and Laboratory of Inorganic Materials Chemistry (CMI) University of Namur 61 rue de Bruxelles B-5000 Namur Belgium. bao-lian.su@unamur.be and Clare Hall University of Cambridge Cambridge CB2 1EW UK. bls26@cam.ac.uk.

Over the last decade, significant effort has been devoted to the applications of hierarchically structured porous materials owing to their outstanding properties such as high surface area, excellent accessibility to active sites, and enhanced mass transport and diffusion. The hierarchy of porosity, structural, morphological and component levels in these materials is key for their high performance in all kinds of applications. The introduction of hierarchical porosity into materials has led to a significant improvement in the performance of materials. Herein, recent progress in the applications of hierarchically structured porous materials from energy conversion and storage, catalysis, photocatalysis, adsorption, separation, and sensing to biomedicine is reviewed. Their potential future applications are also highlighted. We particularly dwell on the relationship between hierarchically porous structures and properties, with examples of each type of hierarchically structured porous material according to its chemical composition and physical characteristics. The present review aims to open up a new avenue to guide the readers to quickly obtain in-depth knowledge of applications of hierarchically porous materials and to have a good idea about selecting and designing suitable hierarchically porous materials for a specific application. In addition to focusing on the applications of hierarchically porous materials, this comprehensive review could stimulate researchers to synthesize new advanced hierarchically porous solids.

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Hydrogen/Electron Amphiphilic Bi-Functional Water Molecular Inactivator-Assisted Interface Stabilization in Highly Reversible Zn Metal Batteries

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Angewandte Chemie 2024年第7期137卷

作者： Wenwei Zhang Dr. Shaohua Zhu Tong Yang Lu Wu Jinghao Li Jiang Liang Dr. Yu Liu Lianmeng Cui Chen Tang Xinran Chen Huiqing Zhou Fan Qiao Min Zhou Prof. Ping Luo Fengtong Chi Dr. Xiaobin Liao Prof. Lei Zhang Prof. Qinyou An State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China The State Key Laboratory of Refractories and Metallurgy and Institute of Advanced Materials and Nanotechnology Wuhan University of Science and Technology Wuhan 430081 China School of Chemistry and Chemical Engineering Shanghai Jiao Tong University 800 Dongchuan Road Shanghai 200240 China School of Materials and Chemical Engineering Hubei University of Technology Wuhan 430068 China Hubei Longzhong Laboratory Wuhan University of Technology (Xiangyang Demonstration Zone) Xiangyang Hubei 441000 China Zhongyu Feima New Material Technology Innovation Center (Zhengzhou) Co. Ltd. High Technology Industrial Development Zone Zhengzhou 450001 China

Continuous hydrogen-bond-network in aqueous electrolytes can lead to uncontrollable hydrogen transfer, and combining the interfacial parasitic electron consumption cause the side reaction in aqueous zinc metal batteries (AZMBs). Herein, hydrogen/electron amphiphilic bi-functional 1,5-Pentanediol (PD) molecule was introduced to stabilize the electrode/electrolyte interface. Stronger proton affinity of -OH in PD can break bulk-H 2 O hydrogen-bond-network to inhibit the activity of water, and electron affinity can enhance electron acceptation capability, which ensures that PD is preferentially bound to electrode material over H 2 O. Besides, the participation of PD in the Zn 2+ solvation structure reduces water content at the solid–liquid interface and promotes uniform deposition process by optimizing Zn 2+ de-solvation energy. Accordingly, dense and vertical zinc texture based on intrinsic steric hindrance effect of PD and formed SEI protective layer to induce stable Zinc anode-electrolyte interface. Moreover, an organic–inorganic shielding water layer was formed at the cathode side to suppress vanadium dissolution in vanadium Oxide. Consequently, Zn//Zn symmetric cell could cycle for more than 5600 hours at 1 mAh cm −2 @1 mA cm −2 (more than 250 hours at 50 °C). Besides, the VO 2 and I 2 cathode all achieved stable cycling performance and former pouch cell could reach average capacity of 0.13 Ah.

关键词： Electrode/electrolyte interface Active-water SEI Electron and proton affinity Cathode dissolution

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