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Single-Entity Collisional Electrochemistry at the Micro-and/or Nano-Interface Between Two Immiscible Electrolyte Solutions
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作者 Li-Fang Yang Jun-Jie Chen +7 位作者 Ling-Yu Chen Si-Qi Jin Tao-Xiong Fang Si-Jia He Liang-Jun Shen Xin-Jian Huang Xiao-Hang Sun Hai-Qiang Deng 《电化学(中英文)》 CAS 2024年第11期1-16,I0001,共17页
Single-entity collisional electrochemistry(SECE)is a branch of single-entity electrochemistry.It can directly characterize entities/particles with single particle resolution through random collisions between particles... Single-entity collisional electrochemistry(SECE)is a branch of single-entity electrochemistry.It can directly characterize entities/particles with single particle resolution through random collisions between particles and electrodes in a solution,and obtain rich physicochemical information,thus becoming one of the frontiers of electroanalytical chemistry in the past two decades.Interestingly,the(micro/nanoscale)sensing electrodes have evolved from a polarizable liquid/liquid(mercury/liquid)interface to a solid/liquid interface and then to a liquid/liquid interface(i.e.,an interface between twoimmiscible electrolyte solutions,ITIES),as if they have completed a cycle(but in fact they have not).ITIES has become the latest sensing electrode in the booming SECE due to its polarizability(up to 1.1 V at the water/a,a,a-trifluorotoluene interface)and high reproducibility.The four measurement modes(direct electrolysis,mediated electrolysis,current blockade,and charge displacement)developed in the realm of SECE at solid/liquid interfaces have also been fully realized at the miniature ITIES.This article will discuss these four modes at the ITIES from the perspectives of basic concepts,operating mechanisms,and latest developments(e.g.,discovery of ionosomes,blockade effect of Faradaic ion transfer,etc.),and look forward to the future development and direction of this emerging field. 展开更多
关键词 Single-entity collisional electrochemistry Interface between two immiscible electrolyte solutions Charge transfer
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A review of strategies to produce a fast-charging graphite anode in lithium-ion batteries
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作者 LIANG Jin QIN Ze +4 位作者 QUAN Zhong HAO Jing QIN Xian-ying LI Bao-hua KANG Fei-yu 《新型炭材料(中英文)》 北大核心 2025年第4期738-765,共28页
Lithium-ion batteries(LIBs)are an electrochemical energy storage technology that has been widely used for portable electrical devices,electric vehicles,and grid storage,etc.To satisfy the demand for user convenience e... Lithium-ion batteries(LIBs)are an electrochemical energy storage technology that has been widely used for portable electrical devices,electric vehicles,and grid storage,etc.To satisfy the demand for user convenience especially for electric vehicles,the development of a fast-charging technology for LIBs has become a critical focus.In commercial LIBs,the slow kinetics of Li+intercalation into the graphite anode from the electrolyte solution is known as the main restriction for fast-charging.We summarize the recent advances in obtaining fast-charging graphite-based anodes,mainly involving modifications of the electrolyte solution and graphite anode.Specifically,strategies for increasing the ionic conductivity and regulating the Li+solvation/desolvation state in the electrolyte solution,as well as optimizing the fabrication and the intrinsic activity of graphite-based anodes are discussed in detail.This review considers practical ways to obtain fast Li+intercalation kinetics into a graphite anode from the electrolyte as well as analysing progress in the commercialization of fast-charging LIBs. 展开更多
关键词 Fast charging GRAPHITE Lithium-ion batteries electrolyte solution SOLVATION
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