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从CuCoS到CuCoS六方纳米片的可控相演变作为析氧反应催化剂。

Controlled phase evolution from CuCoS to CuCoS hexagonal nanosheets as oxygen evolution reaction catalysts.

作者信息

Feng Jingjing, Meng Yu, Lian Zixuan, Fang Liang, Long Ziyao, Li Yongtao, Song Yun

机构信息

Department of Materials Science, Fudan University Shanghai 200433 China.

School of Materials Science and Engineering, Anhui University of Technology Maanshan 243032 China.

出版信息

RSC Adv. 2019 Mar 27;9(17):9729-9736. doi: 10.1039/c9ra00640k. eCollection 2019 Mar 22.

Abstract

Developing cheap and efficient transition metal-based catalysts for the oxygen evolution reaction (OER) plays the key role in large-scale implementation of hydrogen production. However, there is still a lack of effective ways to tune the catalysts performance for the OER reaction from the aspect of structure design and element modulation simultaneously. Herein, a novel CuCoS hexagonal nanosheet has been synthesized through the coprecipitation reaction followed by subsequent vapor sulfidation. Simply mixed with carbon nanotubes (CNTs) during electrode preparation, this CuCoS exhibits an overpotential of 284 mV RHE at a current density of 10 mA cm in 1.0 M KOH. The improved OER performance of the CuCoS electrode can be attributed to the electrocatalytically active sites involved in octahedral coordination structures and further activated by Cu substitution. The encouraging results provide insight into further rational design of transition metal-based electrochemical catalysts towards OER applications.

摘要

开发用于析氧反应(OER)的廉价高效过渡金属基催化剂对大规模制氢的实现起着关键作用。然而,从结构设计和元素调控两方面同时调节催化剂的OER性能仍缺乏有效方法。在此,通过共沉淀反应随后进行气相硫化合成了一种新型的CuCoS六角形纳米片。在电极制备过程中简单地与碳纳米管(CNTs)混合,这种CuCoS在1.0 M KOH中电流密度为10 mA cm时,相对于可逆氢电极(RHE)的过电位为284 mV。CuCoS电极OER性能的提高可归因于八面体配位结构中涉及的电催化活性位点,并通过Cu取代进一步活化。这些令人鼓舞的结果为进一步合理设计用于OER应用的过渡金属基电化学催化剂提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a440/9062190/39e79d1f9142/c9ra00640k-f1.jpg

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