水溶液
还原(数学)
化学
催化作用
无机化学
材料科学
化学工程
物理化学
有机化学
几何学
数学
工程类
作者
Xiaofu Sun,Chunjun Chen,Shoujie Liu,Song Hong,Qinggong Zhu,Qingli Qian,Buxing Han,Jing Zhang,Lirong Zheng
标识
DOI:10.1002/anie.201900981
摘要
Electrochemical reduction of CO2 into energy-dense chemical feedstock and fuels provides an attractive pathway to sustainable energy storage and artificial carbon cycle. Herein, we report the first work to use atomic Ir electrocatalyst for CO2 reduction. By using α-Co(OH)2 as the support, the faradaic efficiency of CO could reach 97.6 % with a turnover frequency (TOF) of 38290 h-1 in aqueous electrolyte, which is the highest TOF up to date. The electrochemical active area is 23.4-times higher than Ir nanoparticles (2 nm), which is highly conductive and favors electron transfer from CO2 to its radical anion (CO2.- ). Moreover, the more efficient stabilization of CO2.- intermediate and easy charge transfer makes the atomic Ir electrocatalyst facilitate CO production. Hence, α-Co(OH)2 -supported atomic Ir electrocatalysts show enhanced CO2 activity and stability.
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