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DOI | 10.1039/d1ee00308a |
In situ built interphase with high interface energy and fast kinetics for high performance Zn metal anodes | |
Chu Y.; Zhang S.; Wu S.; Hu Z.; Cui G.; Luo J. | |
发表日期 | 2021 |
ISSN | 17545692 |
起始页码 | 3609 |
结束页码 | 3620 |
卷号 | 14期号:6 |
英文摘要 | In situconstruction of a multifunctional solid electrolyte interphase (SEI) for Zn anodes is promising to address the dendrite growth and side reactions (corrosion and hydrogen evolution) in aqueous Zn-ion batteries. However, there is a lack of constructive methods for choosing suitable SEI compounds and feasible implementation routes. Here, inspired by the SEI-design for Li-metal batteries, we identified that Zn3(PO4)2with high interface energy could suppress Zn dendrite growth effectively and ZnF2could accelerate the kinetics of Zn2+transference and deposition, and thus constructing a composite SEI mainly composed of Zn3(PO4)2and ZnF2(ZCS) is likely to improve interface deposition and electrode kinetics comprehensively. However, the high redox potential of Zn/Zn2+and H2/H+makes it difficult to develop anin situSEI for Zn anodes in aqueous electrolytesviatraditional electrochemical routes. Considering this dilemma, we take advantage of the instability of KPF6in an aqueous environment and buildin situZCS on the Zn anode through the PF6−anion-induced chemical strategy. Surprisingly, ZCS-Zn exhibits enhanced reversibility with a smooth and compact structure during long-term cycling. Both cumulative capacity (2020 mA h cm−2) and the product of the largest current density and areal capacity (10 mA cm−2× 20 mA h cm−2) applied to ZCS-Zn reach the highest levels compared with those reported in recent reports under mildly acidic conditions. This work paves a new way for designing a desirable SEI on the Zn anode and may also guide the interface engineering of other systems to overcome the intrinsic defects in constructing favorable interphases. © The Royal Society of Chemistry 2021. |
英文关键词 | Anodes; Corrosion; Deposition; Growth kinetics; Kinetics; Redox reactions; Solid electrolytes; Solid-State Batteries; Aqueous environment; Constructive methods; Cumulative capacity; Electrochemical routes; Hydrogen evolution; Interface deposition; Interface engineering; Solid electrolyte interphase; Zinc; aqueous solution; design; electrochemistry; electrode; electrolyte; equipment component; hydrogen; reaction kinetics; redox conditions; zinc |
语种 | 英语 |
来源期刊 | Energy & Environmental Science |
文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/190644 |
作者单位 | Shanghai Key Lab of Advanced High-Temperature Materials and Precision Forming, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China; Key Laboratory for Green Chemical Technology of Ministry of Education, State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin UniversityTianjin 300072, China; Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, China |
推荐引用方式 GB/T 7714 | Chu Y.,Zhang S.,Wu S.,et al. In situ built interphase with high interface energy and fast kinetics for high performance Zn metal anodes[J],2021,14(6). |
APA | Chu Y.,Zhang S.,Wu S.,Hu Z.,Cui G.,&Luo J..(2021).In situ built interphase with high interface energy and fast kinetics for high performance Zn metal anodes.Energy & Environmental Science,14(6). |
MLA | Chu Y.,et al."In situ built interphase with high interface energy and fast kinetics for high performance Zn metal anodes".Energy & Environmental Science 14.6(2021). |
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