Lin Huanlei, Shi Zhangping, He Sina, Yu Xiang, Wang Sinong, Gao Qingsheng, Tang Yi
Department of Chemistry , Jinan University , Guangzhou 510632 , China . Email:
Department of Chemistry , Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials , Laboratory of Advanced Materials and Collaborative Innovation Center of Chemistry for Energy Materials , Fudan University , Shanghai 200433 , China . Email:
Chem Sci. 2016 May 1;7(5):3399-3405. doi: 10.1039/c6sc00077k. Epub 2016 Feb 12.
Exploring efficient noble-metal free electrocatalysts for the hydrogen evolution reaction (HER) is one of the most promising pathways for facing the energy crisis. Herein, MoC-MoC heteronanowires composed of well-defined nanoparticles were accomplished controlled carbonization, showing excellent HER activity, fast kinetic metrics and outstanding stability in both acid and basic electrolytes. In particular, the optimal one consisting of 31.4 wt% MoC displayed a low overpotential ( = 126 and 120 mV for reaching a current density of -10 mA cm), a small Tafel slope (43 and 42 mV dec) and a low onset overpotential (38 and 33 mV) in 0.5 M HSO and 1.0 M KOH, respectively. Such prominent performance, outperforming most of the current noble-metal free electrocatalysts, was ascribed to the carbide surface with an optimized electron density, and the consequently facilitated HER kinetics. This work elucidates a feasible way toward efficient electrocatalysts heteronanostructure engineering, shedding some light on the exploration and optimization of catalysts in energy chemistry.
探索用于析氢反应(HER)的高效无贵金属电催化剂是应对能源危机最有前景的途径之一。在此,通过可控碳化制备了由明确的纳米颗粒组成的MoC-MoC异质纳米线,其在酸性和碱性电解质中均表现出优异的析氢活性、快速的动力学参数和出色的稳定性。特别是,由31.4 wt% MoC组成的最佳样品在0.5 M H₂SO₄和1.0 M KOH中分别显示出低过电位(达到-10 mA cm⁻²电流密度时分别为126和120 mV)、小塔菲尔斜率(43和42 mV dec⁻¹)和低起始过电位(38和33 mV)。这种突出的性能优于目前大多数无贵金属电催化剂,归因于具有优化电子密度的碳化物表面以及由此促进的析氢动力学。这项工作阐明了一种通过异质纳米结构工程制备高效电催化剂的可行方法,为能源化学中催化剂的探索和优化提供了一些启示。