材料科学
电解质
电池(电)
阴极
阳极
离子电导率
氧化还原
储能
双功能
无机化学
化学工程
电极
催化作用
有机化学
物理化学
工程类
物理
功率(物理)
化学
冶金
量子力学
作者
Hua Zhang,Minshen Zhu,Hongmei Tang,Qiongqiong Lu,Ting Yang,Xiaoyu Wang,Bin Chen,Zhe Qu,Xia Wang,Minghao Yu,Daniil Karnaushenko,Daniil Karnaushenko,Yang Huang,Oliver G. Schmidt,Kai Zhang
标识
DOI:10.1016/j.ensm.2023.102791
摘要
Rechargeable Zn-air batteries promise safe energy storage. However, they are limited by the redox potential of O2/O2- chemistry in an alkaline electrolyte, resulting in low operating voltages and therefore insufficient energy density to compete with lithium-ion batteries. The O2/O2- redox potential increases by 0.8 V in an acidic medium, hinting at a way to boost the voltage: an asymmetric electrolyte configuration decoupling acidic and alkaline electrolytes for the air cathode and zinc anode. Such configuration requires a thin and ionically conductive membrane to separate two mutually incompatible electrolytes. Here, we report a Zn ion-exchange membrane with high ionic conductivity of 1.1 mS cm-1, which prevents acid-base neutralization. The highly reversible O2/O2- reaction in the acid is made possible by compositing a cobalt-coordinated porphyrin-based polymeric framework with MXene as a bifunctional electrocatalyst. The asymmetric Zn-air battery operates at voltages up to 1.85 V and cycles for more than 200 h with a material-level energy density of 1350 Wh kg-1, projected to a high device-level energy density of 50 Wh kg-1 (coin cell diameter: 20 mm). The asymmetric configuration withstands pressure up to 4 MPa (∼1200 N), demonstrating excellent structural stability for production and practical applications.
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