材料科学
双功能
海水
合金
休克(循环)
碳热反应
化学工程
冶金
催化作用
有机化学
海洋学
地质学
工程类
化学
内科学
医学
碳化物
作者
Jong Hun Ryu,Jaehyun Park,Jeongwoo Park,Jinhong Mun,Eunmi Im,Ho Jeong Lee,Sung You Hong,Kwangjin An,Geunsik Lee,Young‐Sik Kim,Pil Sung Jo,Seok Ju Kang
标识
DOI:10.1016/j.ensm.2021.11.036
摘要
Seawater batteries consisting of Na anode, Na super-ionic conductor separators, and seawater catholytes have received wide attention because of their theoretical specific capacity of 1160 mAh g −1 and cost-effective Na anode in comparison to rare-earth Li. However, large overpotential during charge and discharge caused by parasitic reactions limits their practical applications. In this work, we employ the bifunctional Pt-Co alloy electrocatalysts produced by carbothermal shock (CTS) method to improve the oxygen evolution and reduction reaction activities of seawater batteries. The CTS induced Pt-Co alloy nanoparticles are well synthesized and dispersed on a carbon current collector within a few s, resulting in improved overpotential and cycle endurance of seawater batteries compared to pristine carbon cathode. In particular, the cell can operate for over 500 h in a seawater catholyte at a fixed capacity of 0.25 mA cm −2 without significant performance degradation. Furthermore, CTS can be readily applied to large-area prismatic seawater battery cells. We observe excellent cyclability in a large-scale seawater battery, suggesting that bifunctional Pt-Co alloy electrocatalysts produced by CTS are viable for use in seawater batteries.
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