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Current Progress and Future Perspectives of Electrolytes for Rechargeable Aluminum-Ion Batteries
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作者 Dongwei Ma Du Yuan +3 位作者 Carlos Ponce de Leon Zheng Jiang Xin Xia Jiahong Pan 《Energy & Environmental Materials》 SCIE EI CAS CSCD 2023年第1期25-42,共18页
Aluminum-ion batteries(AIBs)with Al metal anode are attracting increasing research interest on account of their high safety,low cost,large volumetric energy density(≈8046 mA h cm−3),and environmental friendliness.Spe... Aluminum-ion batteries(AIBs)with Al metal anode are attracting increasing research interest on account of their high safety,low cost,large volumetric energy density(≈8046 mA h cm−3),and environmental friendliness.Specifically,the reversible Al electrostripping/deposition is achieved with the rapid development of room temperature ionic liquids,and rapid progress has been made in fabricating high-performance and durable AIBs during the past decade.This review provides an integrated comprehension of the evolution of AIBs and highlights the development of various non-aqueous and aqueous electrolytes including high-temperature molten salts,room temperature ionic liquids,and gel–polymer electrolytes.The critical issues on the interplay of electrolytes are outlined in terms of the voltage window span,the effective ion species during charge storage(Al 3+or Al x Cl?y)and their underlying charge transfer(e.g.,interfacial transfer and diffusion),and the solid electrolyte interface formation and its role.Following the critical insight,future perspectives on how to practically design feasible AIBs are given. 展开更多
关键词 aluminum-ion batteries electrochemical energy storage electrolytes ionic liquids solid electrolyte interface
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Surface states in TiO2 submicrosphere films and their effect on electron transport 被引量:3
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作者 Li'e Mo Wangchao Chen +4 位作者 Ling Jiang Yong Ding Zhaoqian Li Linhua Hu Songyuan Dai 《Nano Research》 SCIE EI CAS CSCD 2017年第11期3671-3679,共9页
Owing to their special three-dimensional network structure and high specific surface area,TiO2 submicrospheres have been widely used as electron conductors in photoanodes for solar cells.In recent years,utilization of... Owing to their special three-dimensional network structure and high specific surface area,TiO2 submicrospheres have been widely used as electron conductors in photoanodes for solar cells.In recent years,utilization of TiO2 submicrospheres in solar cells has greatly boosted the photovoltaic performance.Inevitably,however,numerous surface states in the TiO2 network affect electron transport.In this work,the surface states in TiO2 submicrospheres were thoroughly investigated by charge extraction methods,and the results were confirmed by the cyclic voltammetry method.The results showed that ammonia can effectively reduce the number of surface states in TiO2 submicrospheres.Furthermore,in-depth characterizations indicate that ammonia shifts the conduction band toward a more positive potential and improves the interfacial charge transfer.Moreover,charge recombination is effectively prevented.Overall,the cell performance is essentially dependent on the effect of the surface states,which affects the electron transfer and recombination process. 展开更多
关键词 surface states TiO2 submicrospheres solar cells charge extraction methods cyclic voltammetry
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有机小分子自组装凝胶网络对准固态染料敏化太阳电池电子动力学的影响机制(英文)
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作者 王露 霍志鹏 +4 位作者 桃李 朱俊 陈双宏 潘旭 戴松元 《Science China Materials》 SCIE EI CSCD 2016年第10期787-796,共10页
本文合成了N,N'-1,5-戊二基双月桂酰胺作为有机小分子凝胶剂,并将其应用于准固态染料敏化太阳电池(QS-DSSC)的电解质材料中.通过偏光显微镜观察到凝胶剂分子在液态电解质中形成交联凝胶网络的原位自组装过程.一方面,凝胶网络对氧化... 本文合成了N,N'-1,5-戊二基双月桂酰胺作为有机小分子凝胶剂,并将其应用于准固态染料敏化太阳电池(QS-DSSC)的电解质材料中.通过偏光显微镜观察到凝胶剂分子在液态电解质中形成交联凝胶网络的原位自组装过程.一方面,凝胶网络对氧化还原电对物理扩散的阻碍效应,加速了电解质/TiO_2光阳极界面的电子复合.另一方面,Li+与凝胶剂分子的酰胺基团发生锂键相互作用,减少了Li+在TiO_2表面的吸附,使TiO_2薄膜内的电子传输加快,电子注入效率(ηinj)降低,TiO_2导带边发生负移.测试表明,凝胶电池的开路电压(Voc)、单色光转化效率(IPCE)和短路电流密度(Jsc)均低于液态电解质制备的染料敏化太阳电池(L-DSSC),与上述分析结果符合,且说明电解质/TiO_2光阳极界面电子复合起了主导作用.108°C的相转变温度保证了凝胶电解质的本征稳定性,使得准固态电池在50°C和一个太阳光照条件下连续1000 h的加速老化实验中表现出优良的光热稳定性. 展开更多
关键词 dye-sensitized solar cells quasi-solid-state low molecular mass organogelator electron kinetics stability
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