化学
电化学
催化作用
二氧化碳
二氧化碳电化学还原
电解
膜
化学工程
无机化学
电极
有机化学
一氧化碳
物理化学
生物化学
电解质
工程类
作者
Bhavin Siritanaratkul,Mark Forster,Francesca Greenwell,Preetam K. Sharma,Eileen Hao Yu,Alexander J. Cowan
摘要
The scaling-up of electrochemical CO2 reduction requires circumventing the CO2 loss as carbonates under alkaline conditions. Zero-gap cell configurations with a reverse-bias bipolar membrane (BPM) represent a possible solution, but the catalyst layer in direct contact with the acidic environment of a BPM usually leads to H2 evolution dominating. Here we show that using acid-tolerant Ni molecular electrocatalysts selective (>60%) CO2 reduction can be achieved in a zero-gap BPM device using a pure water and CO2 feed. At a higher current density (100 mA cm-2), CO selectivity decreases, but was still >30%, due to reversible product inhibition. This study demonstrates the importance of developing acid-tolerant catalysts for use in large-scale CO2 reduction devices.
科研通智能强力驱动
Strongly Powered by AbleSci AI