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LaSrCoO异质结构中原位局部相变的MoSe以及超过1000小时的稳定全水电解。

In-situ local phase-transitioned MoSe in LaSrCoO heterostructure and stable overall water electrolysis over 1000 hours.

作者信息

Oh Nam Khen, Kim Changmin, Lee Junghyun, Kwon Ohhun, Choi Yunseong, Jung Gwan Yeong, Lim Hyeong Yong, Kwak Sang Kyu, Kim Guntae, Park Hyesung

机构信息

Department of Energy Engineering, School of Energy and Chemical Engineering, Low Dimensional Carbon Materials Center, Perovtronics Research Center, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.

Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.

出版信息

Nat Commun. 2019 Apr 12;10(1):1723. doi: 10.1038/s41467-019-09339-y.

Abstract

Developing efficient bifunctional catalysts for overall water splitting that are earth-abundant, cost-effective, and durable is of considerable importance from the practical perspective to mitigate the issues associated with precious metal-based catalysts. Herein, we introduce a heterostructure comprising perovskite oxides (LaSrCoO) and molybdenum diselenide (MoSe) as an electrochemical catalyst for overall water electrolysis. Interestingly, formation of the heterostructure of LaSrCoO and MoSe induces a local phase transition in MoSe, 2 H to 1 T phase, and more electrophilic LaSrCoO with partial oxidation of the Co cation owing to electron transfer from Co to Mo. Together with these synergistic effects, the electrochemical activities are significantly improved for both hydrogen and oxygen evolution reactions. In the overall water splitting operation, the heterostructure showed excellent stability at the high current density of 100 mA cm over 1,000 h, which is exceptionally better than the stability of the state-of-the-art platinum and iridium oxide couple.

摘要

从实际角度来看,开发用于全水解的高效双功能催化剂具有重要意义,这些催化剂应储量丰富、成本效益高且耐用,以缓解与贵金属基催化剂相关的问题。在此,我们介绍一种由钙钛矿氧化物(LaSrCoO)和二硒化钼(MoSe)组成的异质结构,作为用于全水电解的电化学催化剂。有趣的是,LaSrCoO和MoSe异质结构的形成会在MoSe中诱导局部相变,从2H相转变为1T相,并且由于电子从Co转移到Mo,Co阳离子部分氧化使得LaSrCoO更具亲电性。连同这些协同效应,析氢反应和析氧反应的电化学活性均得到显著提高。在全水解操作中,该异质结构在100 mA cm²的高电流密度下超过1000小时表现出优异的稳定性,这比最先进的铂和氧化铱对的稳定性要好得多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53e9/6461638/e90a49f8690b/41467_2019_9339_Fig1_HTML.jpg

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