Guo Xiankun, He Xun, Liu Xuwei, Sun Shengjun, Sun Hang, Dong Kai, Li Tengyue, Yao Yongchao, Xie Ting, Zheng Dongdong, Luo Yongsong, Chen Jie, Liu Qian, Li Luming, Chu Wei, Jiang Zhenju, Sun Xuping, Tang Bo
College of Science, Xihua University, Chengdu, Sichuan, 610054, China.
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, Sichuan, 610054, China.
Small. 2024 Aug;20(31):e2400141. doi: 10.1002/smll.202400141. Epub 2024 Mar 3.
Seawater electrolysis holds tremendous promise for the generation of green hydrogen (H). However, the system of seawater-to-H faces significant hurdles, primarily due to the corrosive effects of chlorine compounds, which can cause severe anodic deterioration. Here, a nickel phosphide nanosheet array with amorphous NiMoO layer on Ni foam (NiP@NiMoO/NF) is reported as a highly efficient and stable electrocatalyst for oxygen evolution reaction (OER) in alkaline seawater. Such NiP@NiMoO/NF requires overpotentials of just 343 and 370 mV to achieve industrial-level current densities of 500 and 1000 mA cm, respectively, surpassing that of NiP/NF (470 and 555 mV). Furthermore, it maintains consistent electrolysis for over 500 h, a significant improvement compared to that of NiP/NF (120 h) and Ni(OH)/NF (65 h). Electrochemical in situ Raman spectroscopy, stability testing, and chloride extraction analysis reveal that is situ formed MoO /PO from NiP@NiMoO during the OER test to the electrode surface, thus effectively repelling Cl and hindering the formation of harmful ClO.
海水电解在绿色氢气(H)的生产方面具有巨大潜力。然而,海水制氢系统面临重大障碍,主要是由于氯化合物的腐蚀作用,这可能导致严重的阳极劣化。在此,报道了一种在泡沫镍(NiP@NiMoO/NF)上具有非晶态NiMoO层的磷化镍纳米片阵列,作为碱性海水中析氧反应(OER)的高效稳定电催化剂。这种NiP@NiMoO/NF分别达到500和1000 mA cm的工业级电流密度时,所需过电位仅为343和370 mV,超过了NiP/NF(470和555 mV)。此外,它能持续稳定电解超过500小时,与NiP/NF(120小时)和Ni(OH)/NF(65小时)相比有显著改善。电化学原位拉曼光谱、稳定性测试和氯离子萃取分析表明,在OER测试过程中,NiP@NiMoO会原位形成MoO /PO 到电极表面,从而有效排斥Cl并阻碍有害ClO的形成。