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Ru-S-Sb/ 黑磷协同界面工程高效电解中性电解质制氢

Interfacial engineering of Ru-S-Sb/antimonene electrocatalysts for highly efficient electrolytic hydrogen generation in neutral electrolyte.

机构信息

Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China.

出版信息

Chem Commun (Camb). 2019 Sep 10;55(73):10884-10887. doi: 10.1039/c9cc05522c.

DOI:10.1039/c9cc05522c
PMID:31436764
Abstract

The development of high-kinetic catalysts for the hydrogen evolution reaction (HER) in a neutral electrolyte is of great importance but unfortunately remains a challenge so far. Herein, we report hybrids with abundant Ru-S-Sb bonds and engineered ultrathin antimonene (Ru-S-Sb/antimonene) as highly kinetic, active, stable electrocatalysts for the HER in an aqueous neutral electrolyte. Experiments and density functional theory (DFT) calculations reveal that Ru-S-Sb bonds coupling with antimonene synergistically work to promote HER activity. The present study brings us one step closer to understand the structure-composition-property relationships and practical electrolytic H2 production.

摘要

发展中性电解质中析氢反应 (HER) 的高动力学催化剂非常重要,但迄今为止,这仍然是一个挑战。在此,我们报告了具有丰富 Ru-S-Sb 键和工程化超薄碲化锑 (Ru-S-Sb/碲化锑) 的混合物,它们作为在水中性电解质中具有高动力学、活性和稳定性的 HER 电催化剂。实验和密度泛函理论 (DFT) 计算表明,Ru-S-Sb 键与碲化锑耦合协同作用,促进了 HER 活性。本研究使我们更进一步地理解了结构-组成-性能关系和实际的电解制氢。

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