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通过气-固合成法对金属间化合物纳米颗粒进行活性位点工程:用于析氢的炭黑负载碲化镍

Active site engineering of intermetallic nanoparticles by the vapour-solid synthesis: carbon black supported nickel tellurides for hydrogen evolution.

作者信息

Garstenauer Daniel, Guggenberger Patrick, Zobač Ondřej, Jirsa Franz, Richter Klaus W

机构信息

Department of Functional Materials & Catalysis, University of Vienna, Josef-Holaubek-Platz 2, 1090 Vienna, Austria.

Vienna Doctoral School in Chemistry, University of Vienna, Währinger Straße 42, 1090 Vienna, Austria.

出版信息

Nanoscale. 2024 Nov 7;16(43):20168-20181. doi: 10.1039/d4nr03397c.

DOI:10.1039/d4nr03397c
PMID:39400230
Abstract

The development and design of catalysts have become a major pillar of latest research efforts to make sustainable forms of energy generation accessible. The production of green hydrogen by electrocatalytic water splitting is dealt as one of the most promising ways to enable decarbonization. To make the hydrogen evolution reaction through electrocatalytic water splitting usable on a large scale, the development of highly-active catalysts with long-term stability and simple producibility is required. Recently, nickel tellurides were found to be an interesting alternative to noble-metal materials. Previous publications dealt with individual nickel telluride species of certain compositions due to the lack of broadly applicable synthesis strategies. For the first time, in this work the preparation of carbon black supported nickel telluride nanoparticles and their catalytic performance for the electrocatalytic hydrogen evolution reaction in alkaline media is presented. The facile vapour-solid synthesis strategy enabled remarkable control over the crystal structure and composition, demonstrating interesting opportunities of active site engineering. Both single- and multi-phase samples containing the Ni-Te compounds NiTe, NiTe, NiTe & NiTe were prepared. Onset potentials and overpotentials of -0.145 V RHE and 315 mV at 10 mA cm respectively were achieved. Furthermore, it was found that the mass activity was dependent on the structure and composition of the nickel tellurides following the particular order: NiTe > NiTe > NiTe > NiTe.

摘要

催化剂的开发和设计已成为近期研究工作的一大支柱,旨在实现可持续能源生成方式。通过电催化水分解生产绿色氢气被视为实现脱碳最具前景的途径之一。为使通过电催化水分解的析氢反应能够大规模应用,需要开发具有长期稳定性且易于生产的高活性催化剂。最近,碲化镍被发现是贵金属材料的一个有趣替代品。由于缺乏广泛适用的合成策略,以往的文献主要研究特定组成的单一碲化镍物种。在这项工作中,首次报道了炭黑负载碲化镍纳米颗粒的制备及其在碱性介质中电催化析氢反应的催化性能。这种简便的气-固合成策略能够对晶体结构和组成进行显著控制,展示了活性位点工程的有趣机遇。制备了包含Ni-Te化合物NiTe、NiTe、NiTe和NiTe的单相和多相样品。分别实现了-0.145 V(相对于可逆氢电极)的起始电位和10 mA cm²时315 mV的过电位。此外,发现质量活性取决于碲化镍的结构和组成,顺序为:NiTe > NiTe > NiTe > NiTe。

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