Anion-functionalized interfacial layer for stable Zn metal anodes

被引:60
作者
Fan, Hefei [1 ,2 ]
Li, Min [1 ]
Wang, Erdong [1 ]
机构
[1] Chinese Acad Sci, Dalian Natl Lab Clean Energy, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Zn metal anodes; UIO-66-SO3H; Dendrites; Corrosion; Zn2+ flux; DESIGN; CHALLENGES; TRANSPORT; MEMBRANES; HYDROGEN; CATHODE; GROWTH;
D O I
10.1016/j.nanoen.2022.107751
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Zinc metal anodes suffer from severe dendrite growth and parasitic hydrogen evolution in aqueous electrolyte, which impede their practical application. Herein, a negatively charged protection layer combining metal-organic framework (UIO-66-SO3H) and flexible sulfonated poly (ether ether ketone) (SPEEK) binder is introduced on the Zn anode to suppress dendrites and side reactions (denoted as USL-Zn). The USL film with zincophilic -SO3- functional groups uniformizes the Zn2+ flux and guides even Zn deposition. In addition, this protective layer functions as a physical barrier and manipulates the local electrolyte structure to mitigate the hydrogen evolution reaction and passivation on Zn anode surface. As a result, USL-Zn electrodes deliver high cycling stability at various current densities and capacities (700 h at 5 mA cm(-2), 5 mAh cm(-2) and 300 h at 10 mA cm(-2), 10 mAh cm-2), and enable high average Coulombic efficiency of 99.34 % (1 mA cm-2 for 1 h). Moreover, enhanced rate capacity and prolonged lifespan can be attained in Zn//VO2 full cells. This proposed strategy provides insight into the design of SEI layers in aqueous batteries and promotes the potential application of Zn metal batteries.
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页数:9
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