Concurrent Electrolysis under Pressured CO2 for Simultaneous CO2 Reduction and Hazardous SO2 Removal

被引:6
|
作者
Pei, Yuhou [1 ]
Wang, Chunling [1 ]
Zhong, Heng [1 ,2 ]
Jin, Fangming [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Ctr Hydrogen Sci, Shanghai 200240, Peoples R China
[3] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
来源
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
electrochemical CO2 reduction; sulfite electrooxidation reaction; high pressure; formate production; concurrent system; HYDROGEN-PRODUCTION; ELECTROCATALYTIC OXIDATION; AQUEOUS-SOLUTIONS; GOLD; NIO; ABSORPTION; DESORPTION; DITHIONATE; CONVERSION; DIOXIDE;
D O I
10.1021/acssuschemeng.2c03407
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although elevating CO2 pressure facilitates electrochemical CO2 reduction reaction (CO2RR), the paired anodic oxygen evolution reaction (OER) can hardly gain the benefit due to its sluggish kinetics at near-neutral pH. Here, we replaced the OER with sulfite electrooxidation reaction (SOR) at near-neutral pH to realize a CO2/sulfite concurrent system, which can serve as a promising strategy for the dual treatments of CO2 and SO2 in flue gas. The anodic SOR reaction catalyzed by the non-noble nanoporous NiO supported on the nickel foam electrode exhibited a voltage saving by similar to 1 V in contrast to the OER at 50 mA cm(-2). On the other hand, BiOI-catalyzed cathodic CO2-to-formate conversion at 20 bar CO2 offered a remarkably broadened potential range and enhanced current density in contrast to the results tested at 1 bar CO2. An overall electricity-to-formate energy conversion efficiency of 65% for the CO2RR + SOR system was successfully obtained at a cell voltage of 1.8 V, which is 20% higher than that of the CO2RR + OER system. Based on these, an efficient and energy-saving full electrolysis system for concurrent electrolysis of CO2RR and SOR at 20 bar CO2 has been successfully constructed.
引用
收藏
页码:12670 / 12678
页数:9
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