Reversible proton conversion manipulating charge engineering for highly stable Zn anode

被引:8
作者
Zheng, Sinan [1 ,2 ]
Zhang, Kun [2 ,3 ]
Luo, Bin [1 ,2 ]
Sun, Leilei [1 ,2 ]
Bao, Zhean [1 ,2 ]
Duan, Guosheng [1 ,2 ]
Huang, Jingyun [1 ,2 ]
Gu, Zhenli [4 ]
Ye, Zhizhen [1 ,2 ]
Wang, Yang [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon & Adv Semicond Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Wenzhou, Wenzhou Key Lab Novel Optoelect & Nano Mat, Wenzhou 325006, Peoples R China
[3] Zhejiang Univ, Inst Thermal Sci & Power Syst, Hangzhou 310027, Peoples R China
[4] XREGEN Res Inst, Hangzhou 310056, Peoples R China
基金
中国国家自然科学基金;
关键词
Zinc ion batteries; Charge engineering; Proton -mediated conversion; Preferred (101) deposition; Interlayer Zn growth; BATTERIES;
D O I
10.1016/j.ensm.2024.103588
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
Grievous Zn dendrites and intricate parasitic reactions tremendously hamper the commercialization of Aqueous Zn metal batteries (AZMBs). Herein, the reversible proton conversion mechanism is reported to achieve longterm stable Zn anode by introducing niacin (NAC) additive into electrolyte. The highly responsive NAC can simultaneously assist Zn2+ transport, manipulate interfacial electrodeposition behaviors, and mitigate waterinduced side reactions. Specifically, protonated NAC (NACH+) tendentiously occupy active water sites to construct an electrostatic shield, adaptively modulating charge carriers (H+ and Zn2+) distribution and reduction barrier of Zn2+ to favor dendrite-free Zn (101) deposition. With the deeper cycling, NAC, the deprotonation of NACH+, further coordinates with Zn2+ to guarantee sufficient Zn2+ transport toward electrodeposition interface through phonon exchange with adsorbed NACH+. The as-modified electrolyte enables a remarkable lifespan of over 3900 h and achieves 750 h under deep cycling (10 mA cm-2, 10 mAh cm-2). This work paves a brand-new path toward achieving high-performance AZMBs.
引用
收藏
页数:10
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