Chen Qi, Wang Kefeng, Qin Jingjing, Wang Songzhu, Wei Wei, Wang Jingge, Shen Qi, Qu Peng, Liu Daosheng
College of Chemistry, Chemical Engineering and Environmental Engineering, Liaoning Shihua University Fushun 113001 Liaoning China
Henan Engineering Center of New Energy Battery Materials, Henan Key Laboratory of Biomolecular Recognition and Sensing, College of Chemistry and Chemical Engineering, Shangqiu Normal University Shangqiu 476000 Henan China
RSC Adv. 2019 May 1;9(24):13486-13493. doi: 10.1039/c9ra02873k. eCollection 2019 Apr 30.
Alkaline hydrogen evolution reaction (HER) requires highly efficient and stable catalytic materials, the engineering of which needs overall consideration of the water dissociation process as well as the intermediate hydrogen adsorption process. Herein, a Ru Se@MoS hybrid catalyst was synthesized by the decoration of MoS with Ru Se nanoparticles through a two-step hydrothermal reaction. Due to the bifunctionality mechanism in which Ru promotes the water dissociation and the nearby Se atoms, unsaturated Mo and/or S atoms act as active sites for the intermediate hydrogen adsorption, the hybrid catalyst exhibits an exceptional HER performance in basic media with a rather low overpotential of 45 mV at a current density of 10 mA cm and a small Tafel slope of 42.9 mV dec. The synergetic effect between Ru Se and MoS not only enables more catalytically active sites, but also increases the inherent conductivity of the hybrid catalyst, leading to more favorable HER kinetics under both alkaline and acidic conditions. As a result, Ru Se@MoS also demonstrates an enhanced catalytic activity toward HER in 0.5 M HSO in comparison with pure Ru Se and MoS, which requires an overpotential of 120 mV to deliver a 10 mA cm current density and gives a Tafel slope of 72.2 mV dec. In addition, the hybrid electrocatalyst also exhibits superior electrochemical stability during the long-term HER process in both acidic media and alkaline media.
碱性析氢反应(HER)需要高效且稳定的催化材料,其设计需要全面考虑水的解离过程以及中间氢吸附过程。在此,通过两步水热反应,用RuSe纳米颗粒修饰MoS合成了RuSe@MoS混合催化剂。由于Ru促进水的解离且附近的Se原子、不饱和Mo和/或S原子作为中间氢吸附的活性位点这种双功能机制,该混合催化剂在碱性介质中表现出优异的HER性能,在电流密度为10 mA cm时过电位相当低,仅为45 mV,塔菲尔斜率为42.9 mV dec。RuSe和MoS之间的协同效应不仅能产生更多催化活性位点,还能提高混合催化剂的固有导电性,从而在碱性和酸性条件下均导致更有利的HER动力学。结果,与纯RuSe和MoS相比,RuSe@MoS在0.5 M HSO中对HER也表现出增强的催化活性,后者在电流密度为10 mA cm时需要120 mV的过电位,塔菲尔斜率为72.2 mV dec。此外,该混合电催化剂在酸性介质和碱性介质中的长期HER过程中也表现出优异的电化学稳定性。