材料科学
铜
纳米孔
碳纤维
乙烯
电解
化学工程
无机化学
纳米技术
催化作用
有机化学
冶金
电极
复合材料
物理化学
复合数
化学
电解质
工程类
作者
Panagiotis Papangelakis,Ali Shayesteh Zeraati,Colin P. O’Brien,Loann Bonnenfant,Roham Dorakhan,Christine M. Gabardo,Daniel Young,Jonathan Kong,Zahra Azimi Dijvejin,Amin Morteza Najarian,Sungjin Park,Heejong Shin,Rui Kai Miao,Alexander H. Ip,Kevin B. Golovin,Edward Hartley Sargent,David A. Sinton
标识
DOI:10.1002/aenm.202400763
摘要
Abstract Electrochemical carbon dioxide (CO2) reduction offers a low‐carbon route to ethylene, when powered from renewable energy. Yet, the best‐performing CO2 electrolysis systems employ neutral or alkaline electrolytes, resulting in low conversion efficiencies, which increases downstream separation costs. High conversion rates can be achieved with acidic electrolytes, albeit at the cost ethylene faradaic efficiency (FE < 45%). As a result, achieving high ethylene selectivity simultaneously with high conversion efficiency is an unmet challenge. Here, a 3D‐nanoporous catalyst is designed to modulate water and CO2 concentration at the catalyst surface, reaching higher ethylene selectivity in a forward‐bias bipolar MEA that recovers unreacted CO2. An ethylene FE of 63% at 150 mA cm−2 is reported, and by optimizing for conversion efficiency, an ethylene FE of 58% along with an overall conversion efficiency of 82% is achieved. Stable performance for > 65 h at industrial current densities combined with a high ethylene concentration in the product stream showcases promising industrial viability.
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