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Unveiling oscillatory nature for sustainable fuel production

National Science Review 2024年第5期11卷 90-91页

作者： Ning Han Ye Wang Bao-Lian Su Department of Materials Engineering State Key Laboratory of Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy Materials National Engineering Laboratory for Green Chemical Productions of Alcohols Ethers and Esters College of Chemistry and Chemical Engineering Xiamen University Laboratory of Inorganic Materials Chemistry(CMI) University of Namur State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology

A century ago, in 1923, Franz Fischer and Hans Tropsch introduced the groundbreaking Fischer–Tropsch (FT) synthesis, a heterogeneous catalytic process used to convert synthesis gas (syngas,CO+H2) into multi-carbon hydrocarbons [1]. Over the past 100 years, FT synthesis has emerged as a pivotal method for converting non-petroleum resources into exceptionally clean fuels or valuable chemicals via syngas [2–4].

关键词： production nature fuel oscillatory sustainable unveiling

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3D ordered macroporous sulfur-doped g-C_(3)N_(4)/TiO_(2)S-scheme photocatalysts for efficient H_(2)O_(2)production in pure water

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Journal of Materials Science & technology 2023年第31期162卷 1-10页

作者： Zicong Jiang Qing Long Bei Cheng Rongan He Linxi Wang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hunan Key Laboratory of Applied Environmental Photocatalysis Changsha UniversityChangsha 410022China Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074China

Photocatalytic hydrogen peroxide(H_(2)O_(2))production offers a clean and cost-efficient alternative to the traditional anthraquinone oxidation ***,a step-scheme(S-scheme)heterojunction photocat-alyst is fabricated by coupling TiO_(2)with three dimensionally ordered macroporous sulfur-doped graphitic carbon nitride(3DOM SCN/T)by electrostatic *** optimized photocatalyst achieved a high photocatalytic H_(2)O_(2)production activity with a yield of 2128μmol h^(−1)g^(−1)without the addition of hole *** remarkable performance was attributed to the synergy between the 3DOM framework and the S-scheme *** former enhances light harvesting and provides abundant active sites for surface reactions,while the latter promotes the spatial separation of photogenerated carriers and enhances the redox ***,the mechanism of photocatalytic H_(2)O_(2)production over the 3DOM SCN/T S-scheme composite is *** work provides novel insights into the development of effi-cient photocatalysts for H_(2)O_(2)production from water and O_(2).

关键词： Photocatalysis Step-scheme heterojunction Three dimensionally ordered macroporous Hydrogen peroxide O_(2)reduction reaction

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Multiscale Anion-Hybrid in Atomic Ni Sites for High-Rate Water Electrolysis: Insights into the Charge Accumulation Mechanism

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Journal of the American Chemical Society 2024年第20期146卷 14194-14202页

作者： Li, Yan Peng, Yanan Dong, Wenda Jiang, Xueyu Lu, Lijun Yang, Dali Hsu, Liang-Ching Li, Wu Su, Baolian Lei, Aiwen Wuhan University Hubei Wuhan430072 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Hubei Wuhan430070 China National Chung Hsing University Taichung40227 Taiwan

Single-atom catalysts, characterized by transition metal-(N/O)4 units on nanocarbon (M-(N/O)4-C), have emerged as efficient performers in water electrolysis. However, there are few guiding principles for accurately controlling the ligand fields of single atoms to further stimulate the catalyst activities. Herein, using the Ni-(N/O)4-C unit as a model, we develop a further modification of the P anion on the outer shells to modulate the morphology of the ligand. The catalyst thus prepared possesses high activity and excellent long-term durability, surpassing commercial Pt/C, RuO2, and currently reported single-atom catalysts. Notably, mechanistic studies demonstrated that the pseudocapacitive feature of multiscale anion-hybrid nanocarbon is considerable at accumulating enough positive charge [Q], contributing to the high oxygen evolution reaction (OER) order (β) through the rate formula. DFT calculations also indicate that the catalytic activity is decided by the suitable barrier energy of the intermediates due to charge accumulation. This work reveals the activity origin of single atoms on multihybrid nanocarbon, providing a clear experiential formula for designing the electronic configuration of single-atom catalysts to boost electrocatalytic performance. © 2024 American Chemical Society.

关键词： Catalyst activity

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Mitigating the capacity fading of Si nanoparticles through V_(2)O_(3) and carbon dual coatings

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Journal of Materials Science & technology 2024年第24期191卷 17-22页

作者： Ruhan He Hao Li Aoyuan Chen Liqiang Mai Liang Zhou State Key Laboratory 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 Hubei Longzhong Laboratory Wuhan University of Technology(Xiangyang Demonstration Zone)Xiangyang 441000China Hainan Institute Wuhan University of TechnologySanya 572000China

Nano-structured silicon(Si)has demonstrated high capacity for lithium storage;however,it suffers from unsatisfactory cycling stability caused by large volume change and poor interface ***,it is very important to construct functional coatings on nano-structured Si to buffer the volume change and improve the interface ***,we successfully construct V_(2)O_(3) and carbon(C)dual-layer coatings on Si nanoparticles with ultrathin and uniform thickness using a facile spray drying and chemical vapour deposition *** as-prepared Si@V_(2)O_(3)@C manifests a high specific capacity of 2230 mAh g^(-1) after 100 cycles under the current density of 200 mA g^(-1),showing its promising application prospect in lithium *** situ electrochemical impedance spectroscopy(EIS)results at different lithiation states and different cycles show a more stable interface resistance of Si@V_(2)O_(3)@C than pristine *** V_(2)O_(3) and C dual coating layers not only ensure the Si nanoparticles with high structural stability by buffering volume expansion and preventing electrolyte penetration,but also guarantee a superior electron transport rate because of the metallic V_(2)O_(3) as well as the highly conductive carbon layers.

关键词： Lithium-ion batteries Silicon anode Vanadium(Ⅲ)oxide Spray drying SEI layer

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High thermoelectric performance of flexible Ag/Ag_(2)Se composite film on nylon for low-grade energy harvesting

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Journal of Materials Science & technology 2024年第12期179卷 79-85页

作者： Ying Liu Jiajia Li Zixing Wang Ping Wei Wenyu Zhao Lidong Chen Kefeng Cai Key Laboratory of Advanced Civil Engineering Materials of Ministry of Education Shanghai Key Laboratory of Development and Application for Metal-Functional MaterialsSchool of Materials Science&EngineeringTongji UniversityShanghai 201804China State Key Laboratory of High Performance Ceramics and Superfine Microstructure Shanghai Institute of CeramicsChinese Academy of SciencesShanghai 200050China University of Chinese Academy of Sciences Beijing 100049China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

In this work,Ag/Ag_(2)Se composite films with excellent thermoelectric(TE)properties and flexibility are prepared based on a simple one-pot *** adjusting the nominal ratios of Ag/Se,an optimal Ag/Ag_(2)Se composite film shows a large power factor of~2275 μW m^(-1) K^(-2) at 300 *** an outstand-ing TE performance of the composite film is due to the unique microstructure and the synergistic effect between the Ag and Ag_(2)***,the composite film also shows outstanding flexibility(~91.8%of the initial electrical conductivity is maintained,and the S is unchanged after 1500 bending cycles with a bending radius of 4 mm).Furthermore,a 4-leg flexible TE generator assembled with the optimal film produces a voltage of 14.06 mV and 4.96 μW at a temperature difference of 30.4 *** work provides a new inspiration for the preparation of flexible Ag_(2)Se-based films with excellent TE performance near room temperature.

关键词： Thermoelectric Ag/Ag_(2)Se Flexible Film Power generator

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Revealing structural degradation in layered structure oxides cathode of lithium ion batteries via in-situ transmission electron microscopy

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Journal of Materials Science & technology 2023年第23期154卷 189-201页

作者： Fanjie Xia Weihao Zeng Haoyang Peng Hong Wang Congli Sun Ji Zou Jinsong Wu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan 430070 China Nanostructural Research Center (NRC) Wuhan University of Technology Wuhan 430070 China Hubei Longzhong Laboratory Xiangyang 441000 China

Transition metal oxides with layered structure have been widely used as cathode materials for lithium-ion batteries(LIBs)which have relatively high energy density,large capacity and long ***,in the long-term electrochemical cycle,the inevitable degradation of performance of LIBs due to structural degradation in cathodes severely restricts their large-scale practical *** the underlying mechanism of structural degradation is the most critical scientific ***,in situ transmission electron microscopy(TEM)has become a useful tool to study the structural and compositional evolutions at atomic scale in electrochemical reactions,which provided a unique and in-depth understanding of the structural *** this review,we discuss the recent advances in the in situ TEM,focusing on its role in revealing the structural degradation mechanisms in the four key places:(1)the interface between the cathodes and electrolyte;(2)the cathode surface;(3)the particle interior and(4)those induced by thermal *** insight gained by the in-situ TEM which is still developing at its fast pace is unique and expected to provide guidance for designing better layered cathode materials.

关键词： Li-ion battery Layered cathodes Structural degradations Electron microscopy In-situ

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In Situ-Constructed Li_(x)MoS_(2)with Highly Exposed Interface Boosting High-Loading and Long-Life Cathode for All-Solid-state Li-S Batteries

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Energy & Environmental Materials 2024年第4期7卷 163-174页

作者： Hao Li Rui Wang Jiangping Song Dan Liu Hongyang Gao Yimin Chao Haolin Tang A State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Department of Chemistry Chemical Engineeringand Life ScienceWuhan University of TechnologyWuhan 430070China Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan 528200China School of Chemistry University of East AngliaNorwich NR47TJUK

As the persistent concerns regarding sluggish reaction kinetics and insufficient conductivities of sulfur cathodes in all-solid-state Li-S batteries(ASSLSBs),numerous carbon additives and solid-state electrolytes(SSEs)have been incorporated into the cathode to facilitate ion/electron pathways around ***,this has resulted in a reduced capacity and decomposition of ***,it is worth exploring neotype sulfur hosts with electronic/ionic conductivity in the ***,we present a hybrid cathode composed of few-layered S/MoS_(2)/C nanosheets(<5 layers)that exhibits high-loading and long-life performance without the need of additional carbon additives in advanced *** multifunctional MoS_(2)/C host exposes the abundant surface for intimate contacting sites,in situ-formed LixMoS_(2)during discharging as mixed ion/electron conductive network improves the S/Li2S conversion,and contributes extra capacity for the part of active *** a high active material content(S+MoS_(2)/C)of 60 wt%in the S/MoS_(2)/C/Li_(6)PS_(5)Cl cathode composite(the carbon content is only~3.97 wt%),the S/MoS_(2)/C electrode delivers excellent electrochemical performance,with a high reversible discharge capacity of 980.3 mAh g^(-1)(588.2 mAh g^(-1)based on the whole cathode weight)after 100 cycles at 100 mA g^(-1).The stable cycling performance is observed over 3500 cycles with a Coulombic efficiency of 98.5%at 600 mA g^(-1),while a high areal capacity of 10.4 mAh cm^(-2)is achieved with active material loading of 12.8 mg cm^(-2).

关键词： all-solid-state lithium-sulfur batteries conversion/intercalation high-loading and long-life low carbon content mixed ionic/electronic conductivities

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Light-enhanced metal-support interaction for synergetic photo/thermal catalytic formaldehyde oxidation

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Journal of Materials Science & technology 2023年第36期167卷 74-81页

作者： Jiawei Ye Linxi Wang Bicheng Zhu Bei Cheng Rongan He Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hunan Key Laboratory of Applied Environmental Photocatalysis Changsha UniversityChangsha 410022China

The strong metal-support interaction(SMSI)plays a pivotal role in regulating electronic properties and activating surface oxygen *** this work,we report light-irradiation-modulated SMSI for enhanced formaldehyde(HCHO)***,the SMSI between Pt nanoparticles(NPs)and Bi_(2)MoO_(6)cre-ated surface-active oxygen at Pt-Bi_(2)MoO_(6)interfaces to activate HCHO to dioxymethylene(DOM).Notably,light irradiation boosted the SMSI and catalytic ***,photogenerated holes in Bi_(2)MoO 6 im-proved HCHO adsorption and activation,while photogenerated electrons migrated from Bi_(2)MoO_(6)to Pt NPs to promote O_(2)adsorption and activation,accelerating the oxidation of DOM to CO_(2)and H_(2)*** light-modulated SMSI and the synergy between photocatalysis and thermocatalysis lead to enhanced cat-alytic oxidation activity,providing a practical strategy for indoor volatile organic compound(VOC)de-composition under ambient conditions.

关键词： Formaldehyde oxidation Strong metal-support interaction Photocatalysis Photo-thermal synergy Electron transfer

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Probing the Nucleation and Growth Kinetics of Bismuth Nanoparticles via In-situ Transmission Electron Microscopy

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Journal of Wuhan University of technology(Materials Science) 2024年第4期39卷 877-887页

作者：王浪李超凡 RAN Maojin YUAN Manman 胡执一 LI Yu State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Nanostructure Research Centre(NRC) Wuhan University of TechnologyWuhan 430070China Institute of Chemistry Henan Academy of SciencesZhengzhou 450002China Henan Academy of Sciences Zhengzhou 450046China

The nucleation and growth mechanism of nanoparticles is an important theory,which can guide the preparation of ***,it is still lacking in direct observation on the details of the evolution of intermediate state structure during nucleation and *** this work,the evolution process of bismuth nanoparticles induced by electron beam was revealed by in-situ transmission electron microscopy(TEM)at atomic *** experimental results demonstrate that the size,stable surface and crystallographic defect have important influences on the growth of Bi *** non-classical growth paths including single crystal growth and polycrystalline combined growth,as well as,corresponding layer-by-layer growth mechanism along{012}stable crystal plane of Bi nanoparticles with dodecahedron structure were revealed by in-situ TEM *** results provide important guidance and a new approach for in-depth understanding of the nucleation and growth kinetics of nanoparticles.

关键词： bismuth nanoparticles crystal growth transmission electron microscopy in-situ electron microscopy

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Reshaping Electrolyte Solvation Structure for High-Energy Aqueous Batteries

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Energy & Environmental Materials 2022年第3期5卷 686-687页

作者： Shuailei Liu Jinping Liu School of Chemistry Chemical Engineering and Life ScienceState Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China

A highlight on reshaping aqueous electrolyte solvation structure for highenergy batteries is ***,the recent key design routes for regulating solvation structure to widen electrochemical stability window(ESW)of aqueous electrolyte are briefly ***,the groundbreaking work of Wang et *** reshaping electrolyte structure using urea as the diluent is ***,the significance of Wang's work is highlighted.

关键词： aqueous electrolyte structure CO(NH_2)_2 electrochemical stability window energy density

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