Affiliation:
1. International Institute for Carbon‐Neutral Energy Research (wpi‐I2CNER) Kyushu University Motooka 744, Nishi‐ku 819‐0395 Fukuoka Japan
2. Department of Applied Chemistry Faculty of Engineering Kyushu University Motooka 744, Nishi‐Ku 819‐0395 Fukuoka Japan
3. International Research Center for Hydrogen Energy Kyushu University Motooka 744, Nishi‐ku 819‐0395 Fukuoka Japan
Abstract
AbstractThe versatility of the spinel (AB2O4) oxides means they are of great interest for a variety of catalysis and energy conversion applications, involving gas reactions and reforming. CuFe2O4 spinel is identified as a highly efficient fuel electrode for CO2/H2O co‐electrolysis due to its promising electrocatalytic activity. To identify the actual active sites, the electrochemical characteristics, composition, chemical state, and microstructure are systematically investigated while optimizing the electrolysis performance by varying the feed gas composition. Markedly enhanced electrolysis current density is achieved under a CO2‐enriched composition of 50%CO2/10%H2O‐Ar. This promising performance is attributed to the in situ exsolution of heterostructural “Cu/Fe3O4” nanoparticles on the parent CuFe2O4 surface during co‐electrolysis. Interestingly, a strong correlation of the electrolysis performance with the amount of the formed heterostructural cermet is observed. The exsolved cermet heterostructure plays a crucial role in CO2/H2O electroreduction, as also confirmed by density‐functional‐theory studies. The self‐exsolved Cu/Fe3O4 nanoparticles present exceptional strength due to a strong interaction between the formed metallic Cu and Fe3O4, enabling the electrode to remain active and stable under such high electrical polarization. The excellent durability and stability of the self‐exsolved heterostructural nanoparticles are clearly confirmed by long‐term operation at high‐working voltage with an outstanding Faradaic efficiency (nearly 100%).
Funder
New Energy and Industrial Technology Development Organization
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment
Cited by
1 articles.
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