电催化剂
过电位
催化作用
材料科学
化学工程
质子交换膜燃料电池
纳米颗粒
阴极
离子交换
纳米技术
无机化学
电极
化学
电化学
离子
有机化学
物理化学
工程类
作者
S. Ramakrishnan,Subramanian Vijayapradeep,S. Selva Chandrasekaran,Jian Huang,S. Karthikeyan,Gutru Rambabu,Natarajan Logeshwaran,Tsuyoshi Miyazaki,Mohamed Mamlouk,Dong Jin Yoo
出处
期刊:Carbon
[Elsevier]
日期:2024-01-15
卷期号:220: 118816-118816
被引量:6
标识
DOI:10.1016/j.carbon.2024.118816
摘要
A high performance and durable electrocatalyst for the cathodic hydrogen evolution reaction (HER) in anion exchange membrane (AEM) water electrolyzers is crucial for the emerging hydrogen economy. Herein, we synthesized Pt–C core-shell nanoparticles (core: Pt nanoparticles, shell: N-containing carbon) were uniformly coated on hierarchical MoS2/GNF using pyrolysis of h-MoS2/GNF with a Pt-aniline complex. The synthesized Pt–C core-shell@h-MoS2/GNF (with 11.3 % Pt loading) showed HER activity with a lower overpotential of 30 mV at 10 mA cm−2 as compared to the benchmark catalyst 20 % Pt–C (41 mV at 10 mA cm−2) with improved durability over 94 h at 10 mA cm−2. Furthermore, we investigated the structural stability and hydrogen adsorption energy for Pt13 cluster, C90 molecule, h-MoS2 sheet, Pt13–C90 core-shell, and Pt13–C90 core-shell deposited h-MoS2 sheets using density functional theory (DFT) simulations. We investigated the Pt–C core-shell@h-MoS2/GNF catalyst active sites during HER performance using in-situ Raman analysis as well as DFT. We fabricated anion exchange membrane (AEM) water electrolyzers with cathode catalysts of Pt–C core-shell@h-MoS2/GNF and evaluated device performance with 0.1 and 1.0 M KOH at 20 and 60 °C. Our work provides a new pathway to design core-shell electrocatalysts for use in AEM water electrolyzers to generate green hydrogen.
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