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Hollow V-Doped CoMx (M = P, S, O) Nanoboxes as Efficient OER Electrocatalysts for Overall Water Splitting

机译:空心V掺杂Comx(M = P,S,O)纳米氧氧氧氧氧氧氧氧氧氧氧氧氧氧氧皂组用于整体水分裂的高效Oer电催化剂

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摘要

Hollow nanostructures with intricate interior and catalytic effects have been the focus of researchers in energy conversion and storage. Although tremendous efforts have been made, the fabrication of well-defined hollow nanostructures has been rarely reported due to the limitations of the synthetic methods. Herein, we have proposed a general synthetic strategy for the construction of V-doped CoMx (M = P, S, O) nanoboxes (NBs), where the doped V effectively modifies the electronic structure of CoMx to provide a favorable surface electrochemical environment for the adsorption of reaction intermediates (*O, *OH, and *OOH), leading to a significant enhancement in electrocatalytic performance. More importantly, the hollow nanostructures can expose abundant surface active areas and promote the chemical adsorption of reactants and intermediates, greatly contributing to the promotion of electrocatalytic performance. Impressively, the optimal V-doped CoS2 NBs show excellent electrocatalytic oxygen evolution reaction (OER) performance with an overpotential of only 290 mV at 10 mA cm(-2), along with outstanding overall water-splitting performance. This work supplies pivotal insights for constructing high-performance OER catalysts on the basis of electronic and geometric engineering.
机译:具有复杂的内部和催化作用的空心纳米结构一直是能量转换和储存研究人员的重点。虽然已经进行了巨大的努力,但由于合成方法的局限性,很少报告定义的空心纳米结构的制造。在此,我们提出了一种用于构建V掺杂Comx(M = P,S,O)纳米氧氧氧氧化物(NBS)的一般合成策略,其中掺杂V有效地改变了Comx的电子结构以提供有利的表面电化学环境反应中间体的吸附(* O,* OH和* OOH),导致电催化性能显着提高。更重要的是,中空纳米结构可以暴露丰富的表面活性区域并促进反应物和中间体的化学吸附,极大地有助于促进电催化性能。令人印象深刻地,最佳的V掺杂COS2 NBS显示出优异的电催化氧气进化反应(OER)性能,其过电位仅为10 mA cm(-2),以及出色的整体水分裂性能。这项工作为在电子和几何工程的基础上提供了构建高性能OER催化剂的关键洞察。

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