Affiliation:
1. College of Chemistry and Environmental Engineering Shenzhen University Shenzhen Guangdong 518060 P. R. China
2. Global Innovative Center of Advanced Nanomaterials College of Engineering Science and Environment University of Newcastle Callaghan NSW 2308 Australia
Abstract
AbstractSpinel oxides with tunable chemical compositions have emerged as versatile electrocatalysts, however their performance is greatly limited by small surface area and low electron conductivity. Here, ultrathin high‐entropy Fe‐based spinel oxides nanosheets are rationally designed (i.e., (Co0.2Ni0.2Zn0.2Mg0.2Cu0.2)Fe2O4; denotes A5Fe2O4) in thickness of ≈4.3 nm with large surface area and highly exposed active sites via a modified sol–gel method. Theoretic and experimental results confirm that the bandgap of A5Fe2O4 nanosheets is significantly smaller than that of ordinary Fe‐based spinel oxides, realizing the transformation of binary spinel oxide from semiconductors to metalloids. As a result, such A5Fe2O4 nanosheets manifest excellent performance for the nitrate reduction reaction (NO3−RR) to ammonia (NH3), with a NH3 yield rate of ≈2.1 mmol h−1 cm−2 at −0.5 V versus Reversible hydrogen electrode, outperforming other spinel‐based electrocatalysts. Systematic mechanism investigations reveal that the NO3−RR is mainly occurred on Fe sites, and introducing high‐entropy compositions in tetrahedral sites regulates the adsorption strength of N and O‐related intermediates on Fe for boosting the NO3−RR. The above findings offer a high‐entropy platform to regulate the bandgap and enhance the electrocatalytic performance of spinel oxides.
Funder
National Natural Science Foundation of China
Department of Education of Guangdong Province
Cited by
8 articles.
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