Metal-coordination chemistry guiding preferred crystallographic orientation for reversible zinc anode

被引:164
作者
Qiu, Meijia [1 ,2 ]
Sun, Peng [2 ]
Qin, Aimiao [3 ]
Cui, Guofeng [1 ]
Mai, Wenjie [2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Key Lab Polymer Composite & Funct Mat, Key Lab Low Carbon Chem & Energy Conservat Guangdo, Guangzhou 510275, Peoples R China
[2] Jinan Univ, Guangdong Prov Engn Technol Res Ctr Vacuum Coating, Dept Phys, Siyuan Lab,Guangzhou Key Lab Vacuum Coating Techno, Jinan 510632, Guangdong, Peoples R China
[3] Guilin Univ Technol, Coll Mat Sci & Engn, Key Lab New Proc Technol Nonferrous Met & Mat, Minist Educ, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-coordination chemistry; Texture modification; Stable Zn anode; ZN; ELECTRODEPOSITION; ELECTROLYTE; MECHANISM; SORBITOL; FILMS;
D O I
10.1016/j.ensm.2022.04.018
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 long-term reversible plating/stripping of Zn anodes is one of the decisive parts inside various Zn based aqueous batteries, but originally restricted by irregular dendrite/by-products issues. Guided by the metal-coordination chemistry, a novel additive, sorbitol (SBT), is introduced into the traditional ZnSO4 electrolyte to achieve preferred (002) orientation growth with stably invertible Zn deposition, while modulate the primary solvation structure for Zn2+ through expelling some active H2O molecules to alleviate common side reactions, simultanously. The robust Zn2+-SBT compound enables a much weaker interaction with (002) than (100) and (101), inducing its slower growth and resulting in its ultimate exposure. With a lower surface energy, the primary (002) on Zn anode surface effectively impedes the occurrence of Zn dendrite and several by-products. Excellent stabilities have finally been realized in Zn-Zn symmetric cells and several kinds of full cells, elucidating its potential in future Zn based devices.
引用
收藏
页码:463 / 470
页数:8
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