Hydrogen evolution by a metal-free electrocatalyst
Data(s) |
28/04/2014
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Resumo |
Electrocatalytic reduction of water to molecular hydrogen via the hydrogen evolution reaction may provide a sustainable energy supply for the future, but its commercial application is hampered by the use of precious platinum catalysts. All alternatives to platinum thus far are based on nonprecious metals, and, to our knowledge, there is no report about a catalyst for electrocatalytic hydrogen evolution beyond metals. Here we couple graphitic-carbon nitride with nitrogen-doped graphene to produce a metal-free hybrid catalyst, which shows an unexpected hydrogen evolution reaction activity with comparable overpotential and Tafel slope to some of well-developed metallic catalysts. Experimental observations in combination with density functional theory calculations reveal that its unusual electrocatalytic properties originate from an intrinsic chemical and electronic coupling that synergistically promotes the proton adsorption and reduction kinetics. |
Identificador | |
Publicador |
Nature Publishing Group |
Relação |
DOI:10.1038/ncomms4783 Zheng, Yao, Jiao, Yan, Zhu, Yihan, Li, Lu Hua, Han, Yu, Chen, Ying, Du, Aijun, Jaroniec, Mietek, & Qiao, Shi Zhang (2014) Hydrogen evolution by a metal-free electrocatalyst. Nature Communications, 5(3783). |
Direitos |
Copyright 2014 Nature Publishing Group Author's Pre-print: author can archive pre-print (ie pre-refereeing) Author's Post-print: subject to Restrictions below, author can archive post-print (ie final draft post-refereeing) Restrictions: •6 months embargo Publisher's Version/PDF: author cannot archive publisher's version/PDF General Conditions: •Authors retain copyright •Published source must be acknowledged and DOI cited •Must link to publisher version •Publisher's version/PDF cannot be used •On author's personal website and institutional repository •If funding agency rules apply, authors may post authors version to their relevant funding body's archive, 6 months after publication |
Fonte |
School of Chemistry, Physics & Mechanical Engineering; Science & Engineering Faculty |
Tipo |
Journal Article |