4.6 Article

MoS2 nanoflowers coupled with ultrafine Ir nanoparticles for efficient acid overall water splitting reaction

Journal

JOURNAL OF ENERGY CHEMISTRY
Volume 87, Issue -, Pages 144-152

Publisher

ELSEVIER
DOI: 10.1016/j.jechem.2023.08.017

Keywords

Ultrafine Ir nanoparticles; MoS2 nanoflowers; Bi-functional electrocatalysts; Water splitting reaction

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In this study, an efficient Ir/MoS2 nanoflowers catalyst was reported for acidic water electrolysis. The catalyst exhibited good catalytic activity and stability, reducing the electrolysis overpotential and achieving a kinetic current density of 10 mA cm-2. The strong metal-support interaction changed the electronic structure of Ir metal and promoted the synergistic catalytic effect between Ir and MoS2 nanoflowers.
Bi-functional electrocatalysts for acid overall water splitting reactions are crucial but still challenging to the development of proton exchange membrane water electrolysis. Herein, an efficient bi-functional cat-alyst of Ir/MoS2 nanoflowers (Ir/MoS2 NFs) catalyst was reported for acidic water electrolysis which can be constructed by coupling three-dimensionally interconnected MoS2 NFs with ultrafine Ir nanoparticles. A more suitable adsorption ability for the H* and *OOH intermediates was revealed, where the Ir sites were proposed as the main active center and MoS2 promoted the charge relocation to electronically mod-ify the interfacial structure. The significant interfacial charge redistribution between the MoS2 NFs and the Ir active sites synergistically induced excellent catalytic activity and stability for the water electrol-ysis reaction. Specifically, the catalyst required overpotentials of 270 and 35 mV to reach a kinetic current density of 10 mA cm-2 for OER and HER, respectively, loading on the glass carbon electrode, with high catalytic kinetics, stability, and catalytic efficiency. A two-electrode system constructed by Ir/MoS2 NFs drove 10 mA cm-2 at a cell voltage of 1.55 V, about 70 mV lower than that of the commercial Pt/C|| IrO2 system. In addition, partial surface oxidation of Ir nanoparticles to generate high-valent Ir species was also found significant to accelerate OER. The enhanced catalytic performance was attributed to the strong metal-support interaction in the Ir/MoS2 NFs catalyst system that changed the electronic structure of Ir metal and promoted the synergistic catalytic effect between Ir and MoS2 NFs. The work presented a novel platform of Ir-catalyst for proton exchange membrane water electrolysis.(c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

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