法拉第效率
电解质
溶解
阴极
插层(化学)
扩散
化学工程
四氟硼酸盐
沉积(地质)
化学
材料科学
无机化学
电极
离子液体
催化作用
物理化学
热力学
物理
工程类
古生物学
生物
生物化学
沉积物
作者
Xinzhe Xue,Zhen Liu,Samuel Eisenberg,Qiu Ren,Dun Lin,Wei Wang,Heng Zhang,Jin Z. Zhang,Xiao Wang,Yat Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-10-13
卷期号:8 (11): 4658-4665
被引量:10
标识
DOI:10.1021/acsenergylett.3c01354
摘要
Electrolytic MnO2 batteries store charges via the Mn2+/MnO2 two-electron transfer process with higher capacity and voltage than conventional one-electron (Zn2+ or H+) intercalation reactions. Yet, the opposite effect of interfacial H+ on the dissolution/deposition processes and the role of interfacial H2O are rarely discussed. Here we introduce tetrafluoroborate (BF4–) into the sulfate-based electrolyte to regulate interfacial H+ and H2O activity. First, BF4– hydrolysis increases the electrolyte's acidity, promoting MnO2 dissolution. Second, BF4– forms H-bond networks with interfacial H2O that assist H+ diffusion while retaining a sufficient H2O supply to facilitate MnO2 deposition. As a result, the cathode-free Zn//MnO2 electrolytic cell achieves a high platform of ∼1.92 V and energy efficiency of ∼84.23%. Significantly, the cell delivers 1000 cycles at 1 C with ∼100% Coulombic efficiency and a high energy efficiency retention of 93.65%. Our findings disclose a new strategy to promote Mn2+/MnO2 platform voltage and energy efficiency.
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