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Synthesis of a MoS(x)–O–PtO(x) Electrocatalyst with High Hydrogen Evolution Activity Using a Sacrificial Counter‐Electrode

Water splitting is considered to be a very promising alternative to greenly produce hydrogen, and the key to optimizing this process is the development of suitable electrocatalysts. Here, a sacrificial‐counter‐electrode method to synthesize a MoS(x)/carbon nanotubes/Pt catalyst (0.55 wt% Pt loading)...

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Detalles Bibliográficos
Autores principales: Zhan, Yingxin, Li, Yi, Yang, Zhi, Wu, Xiongwei, Ge, Mengzhan, Zhou, Xuemei, Hou, Junjie, Zheng, Xiannuo, Lai, Yuchong, Pang, Rongrong, Duan, Huan, Chen, Xi'an, Nie, Huagui, Huang, Shaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402408/
https://www.ncbi.nlm.nih.gov/pubmed/30886796
http://dx.doi.org/10.1002/advs.201801663
Descripción
Sumario:Water splitting is considered to be a very promising alternative to greenly produce hydrogen, and the key to optimizing this process is the development of suitable electrocatalysts. Here, a sacrificial‐counter‐electrode method to synthesize a MoS(x)/carbon nanotubes/Pt catalyst (0.55 wt% Pt loading) is developed, which exhibits a low overpotential of 25 mV at a current density of 10 mA cm(−2), a low Tafel slope of 27 mV dec(−1), and excellent stability under acidic conditions. The theory calculations and experimental results confirm the high hydrogen evolution activity that is likely due to the fact that the S atoms in MoS(x) can be substituted with O atoms during a potential cycling process when using Pt as a counter‐electrode, where the O atoms act as bridges between the catalytic PtO(x) particles and the MoS(x) support to generate a MoS(x)–O–PtO(x) structure, allowing the Pt atoms to donate more electrons thus facilitating the hydrogen evolution reaction process.