Xie Chenxu, Ji Zhengtong, Li Yutong, Wang Wenquan, Zhu Yongfu, Zhao Lijun
Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.
Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):291-299. doi: 10.1016/j.jcis.2024.12.062. Epub 2024 Dec 10.
As a clean energy source with high calorific value and clean products, the research and development of electrocatalysts for overall water splitting is a crucial step. In this study, a Mo-doped NiS modified CeO/Ni(OH) nanorod with oxygen-rich vacancies (CeO/Ni(OH)@Mo-NiS) was synthesized by hydrothermal method. The strong hybridization between Ni-3d and O-2p orbitals at deep energy levels can achieve overall metallic properties. Mo doping regulates the charge redistribution near the Fermi level and optimizes the adsorption of intermediates. Furthermore, the presence of oxygen vacancies facilitates to accelerate electron transfer. Hence, in 1 mol/L of KOH electrolyte, CeO/Ni(OH)@Mo-NiS-2 requires only an overpotential of 111 mV and 280 mV to achieve a current density of 10 mA cm for hydrogen evolution reaction (HER) and 50 mA cm for oxygen evolution reaction (OER), respectively. When used as both cathode and anode as a bifunctional catalyst for overall water splitting, only 1.62 V was required to achieve a current density of 10 mA cm.
作为一种具有高热值和清洁产物的清洁能源,用于全水分解的电催化剂的研发是关键一步。在本研究中,通过水热法合成了具有富氧空位的Mo掺杂NiS修饰CeO/Ni(OH)纳米棒(CeO/Ni(OH)@Mo-NiS)。在深能级处Ni-3d和O-2p轨道之间的强杂化可实现整体金属特性。Mo掺杂调节费米能级附近的电荷重新分布并优化中间体的吸附。此外,氧空位的存在有助于加速电子转移。因此,在1 mol/L的KOH电解质中,CeO/Ni(OH)@Mo-NiS-2在析氢反应(HER)中达到10 mA cm的电流密度仅需111 mV的过电位,在析氧反应(OER)中达到50 mA cm的电流密度仅需280 mV的过电位。当用作全水分解的双功能催化剂同时作为阴极和阳极时,达到10 mA cm的电流密度仅需1.62 V。