Coupling electrocatalytic CO2 reduction with glucose oxidation for concurrent production of formate with high efficiency

格式化 过电位 析氧 电解质 材料科学 催化作用 无机化学 法拉第效率 阳极 化学工程 限制电流 阴极 化学 电极 电化学 有机化学 物理化学 工程类
作者
Runyao Zhao,Yiding Wang,Guipeng Ji,Fengtao Zhang,Yuepeng Wang,Yanfei Zhao,Buxing Han,Zhimin Liu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:486: 150280-150280 被引量:4
标识
DOI:10.1016/j.cej.2024.150280
摘要

Electrocatalytic reduction of CO2 (CO2ER) coupled with the oxygen evolution reaction (OER) is an energy-intensive process that generates low-value oxygen, limiting its industrial application. To overcome this limitation, here we report a membrane electrode assembly (MEA) system that combines CO2ER with glucose electrooxidation (GEOR) to simultaneously produce formate using bismuth subcarbonate and carbon nanotube hybrid (BOC-CNT) and nickel cobalt oxide decorated on carbon fiber paper (NCO-CFP) as the cathode and anode catalysts, respectively. The BOC-CNT catalyst showed excellent electrocatalytic performance for CO2ER to formate, affording a high FEHCOO- of 97.9 % with current density of 360 mA cm−2 at −0.77 V vs. RHE (-580 mV overpotential), and the NCO-CFP catalyst achieved GEOR at 0.99 V (vs. RHE) with FEHCOO- >98 %. The coupled CO2ER//GEOR MEA exhibits a low onset cell voltage of 1.20 V and reaches ultrahigh apparent Faraday efficiency of formate (>190 %) in a wide range from 1.8 to 2.4 V, achieving ∼ 33.3 % energy savings compared to CO2ER//OER with a high formate yield of 0.92 mol g-1h−1 at 100 mA cm−2. Besides, all generated formate can be collected from the electrolyte on the anode side due to the spontaneous migration of formate under electric field, thus reducing cross-contamination from CO2 and alkaline electrolytes. In addition, the coupled CO2ER//GEOR system exhibited good electrocatalytic stability for at least 32 h. This strategy provides an innovative and promising approach for the co-electrolytic transformation of biomass derivatives and CO2 to formate.
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