材料科学
双功能
海水
合金
休克(循环)
化学工程
冶金
催化作用
有机化学
海洋学
医学
内科学
地质学
工程类
化学
作者
Jong Hun Ryu,Jaehyun Park,Jeongwoo Park,Jinhong Mun,Eunmi Im,Ho-Jeong Lee,Sung You Hong,Kwangjin An,Geunsik Lee,Youngsik 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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