Sun Jianpeng, Rao Jianan, Qin Shiyu, Li Xiang, Jia Ru, Huang Kelei, Zheng Yu, Meng Xiangchao
Key Laboratory of Marine Chemistry Theory and Technology (Ministry of Education), College of Chemistry & Chemical Engineering, Ocean University of China, Qingdao, Shandong, 266100, China.
Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, Nanning 530004, China.
Nanoscale. 2025 Jun 5;17(22):13842-13849. doi: 10.1039/d5nr01199j.
Optimizing the performance of in-plane S atoms of MoS is crucial to extend the breadth of application of MoS. Herein, using a simple hydrothermal method, we prepared a novel electrocatalyst of Ru incorporated into trinary-MoS (Ru-MoS) nanoflowers. Ru doping could promote preferential transition from the semiconducting (2H) phase to the metallic (1T and 1T') phase in the basal plane. Density functional theory (DFT) calculations confirmed that Ru incorporated into MoS could optimize the electronic structure, improve the conductivity and optimize H* adsorption in interfacial S sites of trinary-MoS, and facilitate the catalytic hydrogen evolution activity. Moreover, in-plane S sites on the Ru doping 2H/1T' heterostructure have been shown to be highly active sites for trinary-MoS. Benefiting from the good conductivity and activated interfacial S sites in trinary-MoS, the prepared Ru-MoS exhibited superior electrocatalytic activity at 10 mA cm and only required overpotentials of 89 mV and 112 mV in alkaline solution and alkaline seawater, respectively. This work provides a fresh insight into the design of highly-efficient trinary-MoS electrocatalysts.
优化MoS面内S原子的性能对于拓展MoS的应用广度至关重要。在此,我们采用简单的水热法制备了一种新型的钌掺入三元MoS(Ru-MoS)纳米花电催化剂。Ru掺杂可促进基面中从半导体(2H)相到金属(1T和1T')相的优先转变。密度泛函理论(DFT)计算证实,掺入MoS的Ru可优化电子结构、提高导电性并优化三元MoS界面S位点处的H*吸附,从而促进催化析氢活性。此外,Ru掺杂的2H/1T'异质结构上的面内S位点已被证明是三元MoS的高活性位点。得益于三元MoS良好的导电性和活化的界面S位点,制备的Ru-MoS在10 mA cm时表现出优异的电催化活性,在碱性溶液和碱性海水中分别仅需89 mV和112 mV的过电位。这项工作为高效三元MoS电催化剂的设计提供了新的见解。