Reinforcing an interfacial molecular dam through a multifunctional organic electrolyte additive for stable Zn anodes

被引:0
|
作者
Lin, Zhenxin [1 ]
Zhang, Yufei [1 ,2 ]
Lin, Xiaoting [1 ]
Ding, Hanlin [1 ]
Ye, Minghui [1 ,2 ]
Wen, Zhipeng [1 ,2 ]
Tang, Yongchao [1 ,2 ]
Liu, Xiaoqing [1 ,2 ]
Li, Cheng Chao [1 ,2 ]
机构
[1] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[2] Jieyang Ctr, Guangdong Prov Lab Chem & Fine Chem Engn, Jieyang 515200, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1039/d4ta04446k
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
The durability of aqueous zinc-ion batteries (AZIBs) is still impeded due to issues such as dendrite growth, byproduct formation and hydrogen evolution reactions in Zn metal anodes. Herein, we proposed a polydentate ligand, triazole (Ta), as an effective electrolyte additive to prolong the anode stability by its selective adsorption preference and enhanced zinc ion coordination and proton buffering ability. Specifically, Ta induces the formation of an interfacial molecular dam that not only mitigates corrosion via the H2O-deficient electric double-layer (EDL) but also facilitates uniform Zn deposition through its large conjugated planes and zincophilic properties. As a result, a symmetrical cell with the Ta additive exhibits a highly reversible cycle life for 2200 h at 1 mA cm-2 with a capacity of 1 mA h cm-2. Notably, using the Ta/ZnSO4 electrolyte enables stable cycling for 400 h at a high depth-of-discharge (DOD) level of 85%, leading to improved performance in the Zn//alpha-MnO2 full cell with a lifetime of over 2000 cycles. Triazole obstructs water induced corrosion and modulates Zn ion flux through its hydrophobic and zincophilic properties.
引用
收藏
页码:24226 / 24236
页数:11
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