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用于在pH通用环境中高效析氢的铂修饰高熵稀土氧化物

Pt-Modified High Entropy Rare Earth Oxide for Efficient Hydrogen Evolution in pH-Universal Environments.

作者信息

Jiang Yong, Liang Zhong, Fu Hao, Sun Mingzi, Wang Siyuan, Huang Bolong, Du Yaping

机构信息

Tianjin Key Lab for Rare Earth Materials and Applications, Center for Rare Earth and Inorganic Functional Materials, Haihe Laboratory of Sustainable Chemical Transformations, Smart Sensing Interdisciplinary Science Center, School of Materials Science and Engineering, National Institute for Advanced Materials, Nankai University, Tianjin 300350, China.

Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR 999077, China.

出版信息

J Am Chem Soc. 2024 Apr 3;146(13):9012-9025. doi: 10.1021/jacs.3c13367. Epub 2024 Mar 22.

Abstract

The development of efficient and stable catalysts for hydrogen production from electrolytic water in a wide pH range is of great significance in alleviating the energy crisis. Herein, Pt nanoparticles (NPs) anchored on the vacancy of high entropy rare earth oxides (HEREOs) were prepared for the first time for highly efficient hydrogen production by water electrolysis. The prepared Pt-(LaCeSmYErGdYb)O showed excellent electrochemical performances, which require only 12, 57, and 77 mV to achieve a current density of 100 mA cm in 0.5 M HSO, 1.0 M KOH, and 1.0 M PBS environments, respectively. In addition, Pt-(LaCeSmYErGdYb)O has successfully worked at 400 mA cm @ 60 °C for 100 h in 0.5 M HSO, presenting the high mass activity of 37.7 A mg and turnover frequency (TOF) value of 38.2 s @ 12 mV, which is far superior to the recently reported hydrogen evolution reaction (HER) catalysts. Density functional theory (DFT) calculations have revealed that the interactions between Pt and HEREO have optimized the electronic structures for electron transfer and the binding strength of intermediates. This further leads to optimized proton binding and water dissociation, supporting the highly efficient and robust HER performances in different environments. This work provides a new idea for the design of efficient RE-based electrocatalysts.

摘要

开发在宽pH范围内用于电解水制氢的高效稳定催化剂对于缓解能源危机具有重要意义。在此,首次制备了锚定在高熵稀土氧化物(HEREOs)空位上的铂纳米颗粒(NPs)用于高效水电解制氢。制备的Pt-(LaCeSmYErGdYb)O表现出优异的电化学性能,在0.5 M H₂SO₄、1.0 M KOH和1.0 M PBS环境中分别仅需12、57和77 mV即可达到100 mA cm⁻²的电流密度。此外,Pt-(LaCeSmYErGdYb)O在0.5 M H₂SO₄中于60 °C、400 mA cm⁻²下成功工作100 h,呈现出37.7 A mg⁻¹的高质量活性和在12 mV时38.2 s⁻¹的周转频率(TOF)值,这远远优于最近报道的析氢反应(HER)催化剂。密度泛函理论(DFT)计算表明,Pt与HEREO之间的相互作用优化了电子转移的电子结构和中间体的结合强度。这进一步导致质子结合和水离解的优化,支持了在不同环境中高效且稳健的HER性能。这项工作为设计高效的稀土基电催化剂提供了新思路。

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