催化作用
材料科学
化学工程
氢
纳米技术
制氢
可扩展性
化学
纳米颗粒
多相催化
金属
铂金
作者
Huijing Ma,Haifei Wang,Chengcheng Cai,Hongyu Song,Qianqing Guo,Xia Long,Xufang Qian,Yixin Zhao
标识
DOI:10.1038/s41467-026-71498-6
摘要
Low-platinum-loading electrocatalysts, offering both high activity and durability under practical conditions, are essential for sustainable hydrogen production. Here we report a scalable synthesis of a platinum single-site catalyst supported on Ni-N-doped carbon nanotubes, achieved via a facile Ni-driven one-step reduction-displacement of Pt4+. The catalyst NCNT-Ni/Pt features a N2-Pt-Cl2 initial coordination, where the dynamic evolution of Pt-Cl bonds regulates the hydrogen evolution reaction performance. Excitingly, the catalyst demonstrates an overpotential of 7.78 ± 0.86 mV at 10 mA cm–2. With a Pt loading of 6 μg cm–2, it enables industrially relevant proton exchange membrane water electrolysis at 1.63 V@1 A cm–2, with a degradation rate of 3.3 μV h–1, sustained over 4500 h. Coupled with a 21%-efficient photovoltaic module, it delivers a 16.06% solar-to-hydrogen efficiency at industrial-level current density. This study presents a practical strategy for minimizing precious-metal use in the synthesis of industrial-grade hydrogen evolution electrocatalysts. Platinum-based catalysts are essential for sustainable hydrogen production. Here, the authors report a scalable synthesis of a low-platinum catalyst supported on Ni-N-doped carbon nanotubes that maintains high activity and stability for over 4500 h in industrial-scale water electrolysis.
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