顺序沉积 FeNC-Cu 串联二氧化碳还原电催化剂以实现低过电位生产 C2+ 醇

Nattaphon Hongrutai, Saurav Ch Sarma, Yuxiang Zhou, Simon Kellner, Angus Pedersen, Kari Adourian, Helen Tyrrell, Mary P Ryan, Joongjai Panpranot, Jesús Barrio
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引用次数: 0

摘要

串联二氧化碳还原电催化剂结合了选择性产生二氧化碳的材料和铜,能够在低过电位和高选择性条件下产生碳氢化合物。然而,控制 CO 生成催化剂的空间分布和催化活性仍是一项挑战。本研究提出了一种新型串联电催化剂,它克服了简单铜催化剂的局限性,即在低过电位下的选择性和效率。串联电催化剂是通过顺序喷涂协议制备的,使用掺杂 N 的 C 中的单原子铁(FeNC)作为选择性 CO 生成催化剂,并使用商用纳米铜粉。FeNC 对 CO 的高远电效率(在 -0.60 V 对 RHE 时观察到 99%)为 Cu 颗粒提供了高 CO 覆盖率,从而减少了氢气进化,并以比裸 Cu 低得多的过电位选择性地生成乙醇和正丙醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sequential deposition of FeNC–Cu tandem CO2 reduction electrocatalysts towards the low overpotential production of C2+ alcohols
Tandem CO2 reduction electrocatalysts that combine a material that selectively produces CO with Cu are capable of producing hydrocarbons at low overpotentials and high selectivity. However, controlling the spatial distribution and the catalytic activity of the CO-making catalyst remains a challenge. In this work, a novel tandem electrocatalyst that overcomes limitations of simple Cu catalysts, namely selectivity and efficiency at low overpotential, is presented. The tandem electrocatalysts are prepared through a sequential spray coating protocol, using a single atom Fe in N-doped C (FeNC) as the selective CO-producing catalyst and commercial Cu nanopowder. The high faradaic efficiency towards CO of FeNC (99% observed at −0.60 V vs. RHE) provides a high CO coverage to the Cu particles, leading to reduced hydrogen evolution and the selective formation of ethanol and n-propanol at a much low overpotential than that of bare Cu.
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