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原位多孔化的MoS纳米岛增强析氢反应/析氧反应双功能电催化

In Situ Porousized MoS Nano Islands Enhance HER/OER Bifunctional Electrocatalysis.

作者信息

Chen Bo, Hu Ping, Yang Fan, Hua Xingjiang, Yang Fairy Fan, Zhu Fei, Sun Ruiyan, Hao Ke, Wang Kuaishe, Yin Zongyou

机构信息

School of Metallurgy Engineering, National and Local Joint Engineering Research Center for Functional Materials Processing, Xi'an University of Architecture and Technology, Xi'an, 710055, China.

Research School of Chemistry, The Australian National University, Canberra, ACT, 2601, Australia.

出版信息

Small. 2023 Apr;19(14):e2207177. doi: 10.1002/smll.202207177. Epub 2023 Jan 26.

Abstract

2D molybdenum disulfide (MoS ) is developed as a potential alternative non-precious metal electrocatalyst for energy conversion. It is well known that 2D MoS has three main phases 2H, 1T, and 1T'. However, the most stable 2H-phase shows poor electrocatalysis in its basal plane, compared with its edge sites. In this work, a facile one-step hydrothermal-driven in situ porousizing of MoS into self-supporting nano islands to maximally expose the edges of MoS grains for efficient utilization of the active stable sites at the edges of MoS is reported. The results show that such active, aggregation-free nano islands greatly enhance MoS 's hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) bifunctional electrocatalytic activities. At a low overpotential of 248 and 300 mV, the porous MoS nano islands can generate a current density of 10 mA cm in HER and OER, which is much better than typical nanosheet morphology. Surprisingly, the porous MoS nano islands even exhibit better performance than the current commercial RuO catalyst in OER. This discovery will be another effective strategy to promote robust 2H-phase, instead of 1T/1T'-phase, MoS to achieve efficient endurable bifunctional HER/OER, which is expected to further replace precious metal catalysts in industry.

摘要

二维二硫化钼(MoS₂)被开发为一种潜在的用于能量转换的非贵金属替代电催化剂。众所周知,二维MoS₂有2H、1T和1T'三种主要相。然而,最稳定的2H相在其基面的电催化性能与其边缘位点相比很差。在这项工作中,报道了一种简便的一步水热驱动原位使MoS₂多孔化形成自支撑纳米岛的方法,以最大程度地暴露MoS₂晶粒的边缘,从而有效利用MoS₂边缘的活性稳定位点。结果表明,这种活性的、无聚集的纳米岛极大地增强了MoS₂的析氢反应(HER)和析氧反应(OER)双功能电催化活性。在248和300 mV的低过电位下,多孔MoS₂纳米岛在HER和OER中可产生10 mA cm⁻²的电流密度,这比典型的纳米片形态要好得多。令人惊讶的是,多孔MoS₂纳米岛在OER中甚至表现出比目前商业RuO₂催化剂更好的性能。这一发现将是促进稳定的2H相而非1T/1T'相MoS₂实现高效持久双功能HER/OER的另一种有效策略,有望在工业中进一步替代贵金属催化剂。

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