Xu Li, Liu Tong, Liu Dong, Xu Airong, Wang Sicong, Huang Hui, Liu Xiaokang, Sun Mei, Luo Qiquan, Zheng Xusheng, Ding Tao, Yao Tao
National Synchrotron Radiation Laboratory, School of Nuclear Science and Technology, University of Science and Technology of China, Hefei, 230029, P.R. China.
Key Laboratory of Precision and Intelligent Chemistry, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei 230026, P.R. China.
Nano Lett. 2024 Jan 31;24(4):1197-1204. doi: 10.1021/acs.nanolett.3c04049. Epub 2024 Jan 16.
Electrocatalytic reduction of nitrate to ammonia (NORR) is gaining attention for low carbon emissions and environmental protection. However, low ammonia production rate and poor selectivity have remained major challenges in this multi-proton coupling process. Herein, we report a facile strategy toward a novel Fe-based hybrid structure composed of Fe single atoms and FeC atomic clusters that demonstrates outstanding performance for synergistic electrocatalytic NORR. By synchrotron Fourier transform infrared spectroscopy and theoretical computation, we clarify that Fe single atoms serve as the active site for NORR, while FeC clusters facilitate HO dissociation to provide protons (*H) for continued hydrogenation reactions. As a result, the Fe-based electrocatalyst exhibits ammonia Faradaic efficiency of nearly 100%, with a corresponding production rate of 24768 μg h cm at -0.4 V vs RHE, exceeding most reported metal-based catalysts. This research provides valuable guidance toward multi-step reactions.
将硝酸盐电催化还原为氨(NORR)因低碳排放和环境保护而受到关注。然而,在这个多质子耦合过程中,低氨产率和差的选择性仍然是主要挑战。在此,我们报道了一种简便的策略,用于制备由铁单原子和FeC原子簇组成的新型铁基杂化结构,该结构在协同电催化NORR方面表现出优异的性能。通过同步辐射傅里叶变换红外光谱和理论计算,我们阐明了铁单原子作为NORR的活性位点,而FeC簇促进HO解离以提供质子(*H)用于持续的氢化反应。结果,该铁基电催化剂表现出近100%的氨法拉第效率,在相对于可逆氢电极(RHE)为-0.4 V时,相应的产率为24768 μg h cm,超过了大多数报道的金属基催化剂。这项研究为多步反应提供了有价值的指导。