材料科学
法拉第效率
电催化剂
乙烯
催化作用
电解
化学工程
铜
无机化学
镍
电极
电化学
冶金
有机化学
化学
电解质
工程类
物理化学
作者
Yi‐Rung Lin,Dong Un Lee,Shunquan Tan,David M. Koshy,Tiras Y. Lin,Lei Wang,Daniel Corral,Jaime E. Avilés Acosta,José A. Zamora Zeledón,V. A. Beck,Sarah E. Baker,Eric B. Duoss,Christopher Hahn,Thomas F. Jaramillo
标识
DOI:10.1002/adfm.202113252
摘要
Abstract Ethylene is particularly attractive due to its major importance as a feedstock for various applications including the polymer industry. As such, catalyst and electrolyzer developments are crucial to achieve industrially relevant ethylene production and efficiency levels. Here, a tandem electrocatalyst composed of copper nanocubes and nickel‐coordinated nitrogen‐doped carbon (NiNC) is presented, which is integrated into gas diffusion electrodes (GDEs) for direct conversion of vapor‐fed CO 2 into ethylene. Evaluation of tandem GDEs in the vapor‐fed flow electrolyzer shows significantly increased ethylene selectivity in terms of faradaic efficiency and C 2 H 4 /CO ratio compared to a non‐tandem copper GDE. The enhancements are attributed to the increased local CO availability near the copper surface via effective CO 2 to CO conversion on neighboring NiNC. The experimental results are validated by 3D resolved continuum simulations, which show increased flux of higher‐order products with the added CO flux from NiNC. The practical viability of Cu/NiNC catalyst is further evaluated in a membrane electrode assembly electrolyzer, achieving 40% FE toward ethylene at 150 mA cm −2 and 3.2 V. These findings highlight the high selectivity and formation rate of ethylene achieved by successful device integration of the Cu/NiNC catalyst, demonstrating the potential for implementation in large‐scale sustainable CO 2 electrolyzers.
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