材料科学
电池(电)
阴极
Atom(片上系统)
催化作用
密度泛函理论
化学工程
分解
纳米技术
物理化学
热力学
计算化学
有机化学
工程类
嵌入式系统
物理
功率(物理)
化学
计算机科学
作者
Kaige Zhu,Xin Li,Junyoung Choi,Changhyeok Choi,Song Hong,Xinyi Tan,Tai‐Sing Wu,Y. L. Soo,Leiduan Hao,Alex W. Robertson,Yousung Jung,Zhenyu Sun
标识
DOI:10.1002/adfm.202213841
摘要
Abstract The rechargeable Li–CO 2 battery shows great potential in civil, military, and aerospace fields due to its high theoretical energy density and CO 2 capture capability. To facilitate the practical application of Li–CO 2 battery, the design of efficient, low‐cost, and robust non‐noble metal cathodes to boost CO 2 reduction/evolution kinetics is highly desirable yet remains a challenge. Herein, single‐atom cadmium is reported with a Cd‐N 4 coordination structure enable rapid kinetics of both the discharge and recharge process when employed as a cathode catalyst, and thus facilitates exceptional rate performance in a Li–CO 2 battery, even up to 10 A g −1 , and remains stable at a high current density (100 A g −1 ). An unprecedented discharge capacity of 160045 mAh g −1 is attained at 500 mA g −1 . Excellent cycling stability is maintained for 1685 and 669 cycles at 1 A g −1 and capacities of 0.5 and 1 Ah g −1 , respectively. Density functional theory calculations reveal low energy barriers for both Li 2 CO 3 formation and decomposition reactions during the respective discharge and recharge process, evidencing the high catalytic activity of single Cd sites. This study provides a simple and effective avenue for developing highly active and stable single‐atom non‐precious metal cathode catalysts for advanced Li–CO 2 batteries.
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