Wang Yijie, Luo Wenjie, Li Haojie, Cheng Chuanwei
Shanghai Key Laboratory of Special Artificial Microstructure Materials and Technology, School of Physics Science and Engineering, Tongji University, Shanghai 200092 P. R. China
Nanoscale Adv. 2021 Jul 22;3(17):5068-5074. doi: 10.1039/d1na00424g. eCollection 2021 Aug 25.
The construction of highly-active and stable electrocatalysts for the hydrogen evolution reaction (HER) is significant for efficient water splitting processes. Herein, we develop an efficient HER catalyst of ultrafine Ru nanoclusters supported on a N/S doped macroporous hollow carbon sphere (Ru/H-S,N-C). The N/S co-doping strategy not only facilitates the reduction of the Ru nanocluster sizes, but also regulates the electronic structure of metallic Ru, improving the HER activity of the metallic Ru catalyst. Due to the structural advantages of N/S-doped macroporous carbon spheres that provide a fast mass transfer process and the high intrinsic activity of Ru nanoclusters, the optimized Ru/H-S,N-C catalyst exhibits excellent HER performance in alkaline medium, with a low overpotential of 32 mV to reach 10 mA cm, fast HER kinetics (a Tafel slope of 24 mV dec) and excellent durability, superior to the performances of the Ru/H-N-C sample and commercial Pt/C catalyst. Our work offers some guidance on the design of efficient Ru-based electrocatalysts.
构建用于析氢反应(HER)的高活性和稳定的电催化剂对于高效的水分解过程具有重要意义。在此,我们开发了一种负载在N/S掺杂的大孔空心碳球(Ru/H-S,N-C)上的高效HER催化剂——超细Ru纳米团簇。N/S共掺杂策略不仅有助于减小Ru纳米团簇的尺寸,还能调节金属Ru的电子结构,提高金属Ru催化剂的HER活性。由于N/S掺杂的大孔碳球的结构优势提供了快速的传质过程以及Ru纳米团簇的高本征活性,优化后的Ru/H-S,N-C催化剂在碱性介质中表现出优异的HER性能,达到10 mA cm时过电位低至32 mV,HER动力学快(塔菲尔斜率为24 mV dec)且耐久性优异,优于Ru/H-N-C样品和商业Pt/C催化剂的性能。我们的工作为高效Ru基电催化剂的设计提供了一些指导。