Liu Pengfei, Cheng Xuetao, Zhao Huilin, Bai Fenghua, Wang Yan-Qin
Inner Mongolia Key Laboratory of Rare Earth Catalysis College of Chemistry and Chemical Engineering Inner Mongolia University Hohhot 010021, P. R. China.
ACS Appl Mater Interfaces. 2025 Jan 8;17(1):980-990. doi: 10.1021/acsami.4c16144. Epub 2024 Dec 18.
Electrocatalytic nitrate reduction (ENORR) for ammonia production is one of the potential alternatives to Haber-Bosch technology for the realization of artificial ammonia synthesis. However, efficient ammonia production remains challenging due to the complex electron transfer process in ENORR. In this study, we fabricated a CuP/CoP heterostructure on carbon cloth (CC) by electrodeposition and vapor deposition, which exhibits an exceptional ENORR performance in alkaline medium, and showcases a Faradaic efficiency of ammonia (FE) and an ammonia yield rate as high as 97.95% and 17,637.3 μg h cm at -0.9 V vs RHE. Moreover, CuP/CoP also has excellent catalytic activity for nitrite reduction to ammonia, with an FE up to 98.31% at -0.7 V vs RHE. The experimental and theoretical calculations reveal and confirm that the formation of a heterogeneous interface between CuP and CoP effectively promotes the electron transfer, where CuP as an electron donor induces the decrease of electron density around Cu and results in an enhancement of NO adsorption, thereby accelerating the ENORR process while inhibiting the competitive hydrogen evolution reaction (HER). Moreover, the metal phosphide catalyst facilitates the water dissociation, which accelerates the abundant *H generation, thus enhancing the subsequent hydrogenation process toward ENORR.
用于氨生产的电催化硝酸盐还原(ENORR)是实现人工合成氨的哈伯-博施法的潜在替代方法之一。然而,由于ENORR中复杂的电子转移过程,高效生产氨仍然具有挑战性。在本研究中,我们通过电沉积和气相沉积在碳布(CC)上制备了CuP/CoP异质结构,该结构在碱性介质中表现出优异的ENORR性能,在相对于可逆氢电极(RHE)为-0.9 V时,氨的法拉第效率(FE)和氨产率高达97.95%和17637.3 μg h cm。此外,CuP/CoP对亚硝酸盐还原为氨也具有优异的催化活性,在相对于RHE为-0.7 V时,FE高达98.31%。实验和理论计算揭示并证实,CuP和CoP之间异质界面的形成有效地促进了电子转移,其中CuP作为电子供体导致Cu周围电子密度降低,从而增强了NO吸附,进而加速了ENORR过程,同时抑制了竞争性析氢反应(HER)。此外,金属磷化物催化剂促进了水的解离,加速了大量*H的生成,从而增强了随后向ENORR的氢化过程。