阴极
法拉第效率
锰
水溶液
溶解
阳极
锌
磷酸盐
电子转移
质子
材料科学
无机化学
解吸
电极
化学
化学工程
吸附
光化学
物理
有机化学
工程类
物理化学
量子力学
作者
Yaozhi Liu,Zengming Qin,Xianpeng Yang,Jie Liu,Xiaoxia Liu,Xiaoqi Sun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-04-26
卷期号:7 (5): 1814-1819
被引量:53
标识
DOI:10.1021/acsenergylett.2c00777
摘要
MnO2 cathodes typically undergo one-electron transfer in aqueous zinc batteries. The two-electron MnO2/Mn2+ reaction provides double capacity and higher voltage. However, this requires a highly acidic environment, which challenges the Zn metal anode. Herein, we present a proton reservoir for the MnO2/Mn2+ reaction. Zinc hydrophosphate is codeposited with MnO2 at the cathode. The former deprotonates to release protons and enhances the reduction of MnO2 to Mn2+. The resulting zinc phosphate further interacts with MnO2 and realizes spontaneous water desorption from the MnO2 surface as revealed by theoretical calculations, which facilitates the dissolution process. The hydrophosphate species is reversibly generated upon charge. Based on this reaction mechanism, the cathode achieves a high discharge voltage of 1.75 V. It also delivers 0.99 mAh cm–2 capacity with 99% Coulombic efficiency. Stable capacity retention is realized for over 3000 cycles. This work demonstrates an effective strategy to access the two-electron process of MnO2 cathode materials in aqueous zinc batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI