Lili Wang , Wurigamula He , Duanduan Yin , Qianli Ma , Wensheng Yu , Ying Yang , Xiangting Dong
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引用次数: 0
Abstract
Urea electrolysis can replace water electrolysis as the anode reaction, reducing the voltage required for hydrogen production and mitigating urea-induced environmental pollution. In this work, we synthesized NMOH (NiMoO4·xH2O) nanorod arrays on nickel foam (NF) via a hydrothermal method and then constructed an NMOH@Pi heterostructure through high-temperature phosphating, where Pi represented phosphate components of the shell. The heterointerface between NMOH and Pi enhances electronic interactions, improving electrical conductivity, intermediate adsorption, and reaction kinetics. Additionally, the super-hydrophilicity and super-aerophobicity of NMOH@Pi/NF enhance electrolyte immersion and bubble detachment, promoting mass transport. The Ni active sites are modulated by Mo, P, and O atoms, preventing further oxidation of Ni2+ during urea oxidation. Phosphorus doping stabilizes oxygen vacancies (Ov), improving catalytic performance. By the aid of the above designed favorable factors, the NMOH@Pi/NF catalyst achieves UOR and HER current densities of 100 mA cm−2 at only 1.410 and 0.176 V, respectively. This work provides new insights for designing bimetallic or multimetallic synergistic electrocatalysts.
尿素电解可以代替水电解作为阳极反应,降低制氢所需的电压,减轻尿素引起的环境污染。本文通过水热法在泡沫镍(NF)上合成了NMOH (NiMoO4·xH2O)纳米棒阵列,并通过高温磷化构建了NMOH@Pi异质结构,其中Pi代表壳的磷酸盐组分。NMOH和Pi之间的异质界面增强了电子相互作用,改善了电导率、中间吸附和反应动力学。此外,NMOH@Pi/NF的超亲水性和超疏气性增强了电解质浸泡和气泡脱离,促进了质量的运输。Ni活性位点由Mo、P和O原子调节,防止了尿素氧化过程中Ni2+的进一步氧化。磷的掺杂稳定了氧空位(Ov),提高了催化性能。在上述有利因素的帮助下,NMOH@Pi/NF催化剂在1.410 V和0.176 V下的UOR和HER电流密度分别达到100 mA cm - 2。本研究为双金属或多金属协同电催化剂的设计提供了新的思路。
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