Selective Electrochemical CO2 Reduction to Ethylene and Multi-carbon Products on Oxide-derived Porous CuO Micro-cages

被引:0
作者
Dabaro, Mintesinot Dessalegn [1 ]
Bandal, Harshad Anil [1 ]
Kim, Hern [1 ]
机构
[1] Myongji Univ, Environm Waste Recycle Inst, Dept Energy Sci & Technol, Yongin 17058, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Porous CuO micro-cages; CO2RR; Faradaic efficiency; Ethylene selectivity; Multi-carbon products; Hydroxide adsorption; CARBON-DIOXIDE; COPPER-CATALYSTS; ELECTROREDUCTION; CO3O4; GENERATION; EFFICIENCY;
D O I
10.1016/j.jiec.2024.10.071
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical reduction of CO2 (CO2RR) presents a dual benefit: it helps mitigate environmental pollution while producing valuable multi-carbon (C2+) chemicals and storing renewable energy in chemical fuels. However, there is an urgent need for efficient electrocatalysts that can selectively increase the production of ethylene and C2+ products for the wide-scale implementation of CO2RR. Herein, we have facilely synthesized porous micro-caged oxide-derived copper oxide (OD-Cu MC) using a one-pot hydrothermal approach followed by air- annealing at 350 degrees C. The resulting electrocatalyst exhibited excellent performance for ethylene (C2H4) production, achieving a faradaic efficiency (FE) of 44.8 % for C2H4 and cumulative FE of 73.1 % for C2+ products at current density (ID) of 300 mA cm- 2. At an ID of 400 mA cm- 2, OD-Cu MC demonstrated a turnover frequency (TOF) of 0.012 s-1 for ethylene, which is 7.8 times higher than the TOF observed for commercially available copper oxide (CuO-CM). Moreover, at an ID of 300 mA cm- 2, OD-Cu MC achieved a single-pass CO2 conversion (SPCC) of 35.2 % and a half-cell energy efficiency of 15.6 % for C2+ products. The catalyst also showed good stability, maintaining its performance for over 4 h at an ID of 200 mA cm- 2. This straightforward synthesis approach opens new avenues for enhancing C2+ product selectivity in CO2RR.
引用
收藏
页码:767 / 775
页数:9
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