Manipulating Interfacial Dissolution-Redeposition Dynamics to Resynthesize Electrode Surface Chemistry

被引:4
作者
Hu, Anyang [1 ]
Zhang, Yuxin [1 ]
Yang, Fan [2 ]
Hwang, Sooyeon [3 ]
Sainio, Sami [4 ,5 ]
Nordlund, Dennis [4 ]
Maxey, Evan [6 ]
Dai, Qilin [7 ]
Gu, Jing [2 ]
Li, Luxi [6 ]
Lin, Feng [1 ]
机构
[1] Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA
[2] San Diego State Univ, Dept Chem & Biochem, San Diego, CA 92181 USA
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[4] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA 94025 USA
[5] Univ Oulu, Fac Informat Technol & Elect Engn, Microelect Res Unit, Oulu 90570, Finland
[6] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[7] Jackson State Univ, Dept Chem Phys & Atmospher Sci, Jackson, MS 39217 USA
基金
欧盟地平线“2020”; 美国国家科学基金会;
关键词
LI-ION BATTERIES; CATHODE MATERIALS;
D O I
10.1021/acsenergylett.2c01186
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 solid-liquid electrochemical interface offers a reactive environment for interfacial reactions to tailor electrode surface chemistry under operating conditions. Herein, we demonstrate that the dissolution and redeposition kinetics of transition metal cations, a ubiquitous phenomenon at the electrochemical interface, can be manipulated to regulate the chemical composition and crystal structure of the electrode surface, as well as the overall electrochemical performance. Foreign cations (e.g., Ti4+) either added as electrolyte additives or dissolved from surface coatings, can rapidly participate in the electrode dissolution-redeposition process and facilitate the establishment of the dissolution-redeposition equilibrium. Our work expands the control over the electrochemical reactions at the solid-liquid interface and provides new insights into interfacial studies in electrochemistry and surface science.
引用
收藏
页码:2588 / 2594
页数:7
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