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具有晶格氢参与的钯氢化物金属烯气凝胶用于高效析氢反应。

Pd hydride metallene aerogels with lattice hydrogen participation for efficient hydrogen evolution reaction.

作者信息

Wang Hengjia, Qin Ying, Wu Yu, Qiu Yiwei, Ling Ling, Fang Qie, Wang Canglong, Hu Liuyong, Gu Wenling, Zhu Chengzhou

机构信息

State Key Laboratory of Green Pesticide, International Joint Research Center for Intelligent Biosensing Technology and Health, College of Chemistry, Central China Normal University, Wuhan, P. R. China.

Institute of Modern Physics, Chinese Academy of Science, Lanzhou, P. R. China.

出版信息

Nat Commun. 2024 Nov 27;15(1):10289. doi: 10.1038/s41467-024-54601-7.

Abstract

Hydrogen adsorption and desorption in single-phase catalysts often occur at a single catalytic site based on the traditional hydrogen evolution reaction (HER) pathway, which makes it difficult to break the limitation entailed by the Sabatier principle. Herein, β-Pd hydride metallene (β-PdHene) aerogels are synthesized as advanced HER catalysts. A lattice hydrogen-involved mechanism is reported to separate adsorption and desorption sites, which is thermodynamically favorable compared to the traditional reaction pathway. In situ differential electrochemical mass spectrometry and theoretical calculations reveal that lattice hydrogen as additional active sites directly participate in the HER process. Consequently, β-PdHene aerogels exhibit a low overpotential of only 20 mV at 10 mA cm and remarkable HER stability, which are even comparable to commercial Pt/C. Our work opens an avenue to rationally develop highly active HER catalysts, bypassing the design limitations of catalysts under traditional mechanisms.

摘要

基于传统析氢反应(HER)途径,单相催化剂中的氢吸附和解吸通常发生在单一催化位点,这使得突破萨巴蒂尔原理带来的限制变得困难。在此,合成了β-钯氢化物金属烯(β-PdHene)气凝胶作为先进的HER催化剂。据报道,一种涉及晶格氢的机制可分离吸附和解吸位点,与传统反应途径相比,该机制在热力学上更有利。原位差分电化学质谱和理论计算表明,晶格氢作为额外的活性位点直接参与HER过程。因此,β-PdHene气凝胶在10 mA cm时仅表现出20 mV的低过电位和出色的HER稳定性,甚至可与商业Pt/C相媲美。我们的工作开辟了一条合理开发高活性HER催化剂的途径,绕过了传统机制下催化剂的设计限制。

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