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用于水分解的原子尺度电催化剂的结构与性能之间的关系

Relationship between Structure and Performance of Atomic-Scale Electrocatalysts for Water Splitting.

作者信息

Choi Jungsue, Seo Sohyeon, Kim Minsu, Han Yeonsu, Shao Xiaodong, Lee Hyoyoung

机构信息

Department of Chemistry, Sungkyunkwan University (SKKU), Suwon, 16419, Republic of Korea.

Creative Research Institute (CRI), Sungkyunkwan University (SKKU), Suwon, 16419, Republic of Korea.

出版信息

Small. 2024 Sep;20(39):e2304560. doi: 10.1002/smll.202304560. Epub 2023 Aug 6.

Abstract

Atomic-scale electrocatalysts greatly improve the performance and efficiency of water splitting but require special adjustments of the supporting structures for anchoring and dispersing metal single atoms. Here, the structural evolution of atomic-scale electrocatalysts for water splitting is reviewed based on different synthetic methods and structural properties that create different environments for electrocatalytic activity. The rate-determining step or intermediate state for hydrogen or oxygen evolution reactions is energetically stabilized by the coordination environment to the single-atom active site from the supporting material. In large-scale practical use, maximizing the loading amount of metal single atoms increases the efficiency of the electrocatalyst and reduces the economic cost. Dual-atom electrocatalysts with two different single-atom active sites react with an increased number of water molecules and reduce the adsorption energy of water derived from the difference in electronegativity between the two metal atoms. In particular, single-atom dimers induce asymmetric active sites that promote the degradation of HO to H or O evolution. Consequently, the structural properties of atomic-scale electrocatalysts clarify the atomic interrelation between the catalytic active sites and the supporting material to achieve maximum efficiency.

摘要

原子尺度的电催化剂极大地提高了水分解的性能和效率,但需要对支撑结构进行特殊调整,以锚定和分散金属单原子。在此,基于不同的合成方法和结构特性,对用于水分解的原子尺度电催化剂的结构演变进行了综述,这些合成方法和结构特性为电催化活性创造了不同的环境。析氢或析氧反应的速率决定步骤或中间状态通过与支撑材料中单个原子活性位点的配位环境在能量上得到稳定。在大规模实际应用中,最大化金属单原子的负载量可提高电催化剂的效率并降低经济成本。具有两个不同单原子活性位点的双原子电催化剂与更多数量的水分子发生反应,并因两个金属原子之间电负性的差异而降低水的吸附能。特别是,单原子二聚体诱导出不对称活性位点,促进了羟基分解为氢气或氧气的过程。因此,原子尺度电催化剂的结构特性阐明了催化活性位点与支撑材料之间的原子相互关系,以实现最高效率。

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