Chen Zhaoyang, Li Lingtong, Chu Youqun, Zhao Fengming, Zhu Yinghong, Tong Shaoping, Zheng Huajun
Cooperation Base of Energy Materials and Application, Petroleum and Chemical Industry Key Laboratory of Organic Electrochemical Synthesis, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang, 310014, China.
Small. 2024 Jun;20(26):e2309675. doi: 10.1002/smll.202309675. Epub 2024 Jan 23.
This study presents a novel approach to enhance the catalytic activity of composite materials by promoting active surface exposure and improving hydrogen transfer performance. Through a self-assembly route involving tailored gas-solid and galvanic replacement reactions, Pt-WC/CNT catalysts with superhydrophilicity and coronavirus-like structure are synthesized. These unique structural features contribute to a remarkable enhancement in the electrocatalytic performance of the hydrogen evolution reaction (HER). Notably, the Pt-WC/CNT catalyst exhibits an outstanding intrinsic activity and efficient bubble transfer properties, leading to a high turnover frequency of 34.97 H·s at an overpotential of 100 mV. This value is 4.8 times higher than that achieved by commercial Pt/C catalysts (7.30 H·s), establishing Pt-WC/CNT as one of the most active catalysts reported to date. Moreover, the combination of gas-solid and galvanic replacement reactions in the synthesis process offers a scalable route for the production of Pt-loading controllable composite catalysts, thus challenging the dominance of commercial Pt/C catalysts.
本研究提出了一种通过促进活性表面暴露和改善氢转移性能来提高复合材料催化活性的新方法。通过涉及定制气固和电化学生成置换反应的自组装路线,合成了具有超亲水性和类冠状病毒结构的Pt-WC/CNT催化剂。这些独特的结构特征显著提高了析氢反应(HER)的电催化性能。值得注意的是,Pt-WC/CNT催化剂表现出出色的本征活性和高效的气泡转移性能,在100 mV的过电位下实现了34.97 H·s的高周转频率。该值比商业Pt/C催化剂(7.30 H·s)高出4.8倍,使Pt-WC/CNT成为迄今为止报道的活性最高的催化剂之一。此外,合成过程中气固和电化学生成置换反应的结合为生产Pt负载可控的复合催化剂提供了一种可扩展的途径,从而挑战了商业Pt/C催化剂的主导地位。