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无粘结剂CoFeO纳米颗粒的可控电泳沉积策略作为析氧反应的增强电催化剂

Controlled Electrophoretic Deposition Strategy of Binder-Free CoFeO Nanoparticles as an Enhanced Electrocatalyst for the Oxygen Evolution Reaction.

作者信息

Lee Gahyeon, Jeong Minsik, Kim Hye Ri, Kwon Minsol, Baek Seulgi, Oh Sekwon, Lee Minhyung, Lee Dongju, Joo Jong Hoon

机构信息

School of Earth Sciences and Environmental Engineering, Gwangju Institute of Science and Technology, Gwangju61005, Republic of Korea.

Department of Urban, Energy, and Environmental Engineering, Chungbuk National University, 1 Chungdae-ro, Seowon-gu, Cheongju, Chungbuk28644, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2022 Nov 2;14(43):48598-48608. doi: 10.1021/acsami.2c11456. Epub 2022 Oct 18.

Abstract

The kinetic-sluggish oxygen evolution reaction (OER) is the main obstacle in electrocatalytic water splitting for sustainable production of hydrogen energy. Efficient water electrolysis can be ensured by lowering the overpotential of the OER by developing highly active catalysts. In this study, a controlled electrophoretic deposition strategy was used to develop a binder-free spinel oxide nanoparticle-coated Ni foam as an efficient electrocatalyst for water oxidation. Oxygen evolution was successfully promoted using the CoFeO catalyst, and it was optimized by modulating the electrophoretic parameters. When optimized, CoFeO nanoparticles presented more active catalytic sites, superior charge transfer, increased ion diffusion, and favorable reaction kinetics, which led to a small overpotential of 287 mV for a current density of 10 mA cm, with a small Tafel slope of 43 mV dec. Moreover, the CoFeO nanoparticle electrode exhibited considerable long-term stability over 100 h without detectable activity loss. The results demonstrate promising potential for large-scale water splitting using Earth-abundant oxide materials via a simple and cheap fabrication process.

摘要

动力学迟缓的析氧反应(OER)是可持续生产氢能的电催化水分解过程中的主要障碍。通过开发高活性催化剂降低OER的过电位,可以确保高效的水电解。在本研究中,采用可控的电泳沉积策略,制备了一种无粘结剂的尖晶石氧化物纳米颗粒包覆泡沫镍作为水氧化的高效电催化剂。使用CoFeO催化剂成功促进了析氧反应,并通过调节电泳参数对其进行了优化。优化后的CoFeO纳米颗粒具有更多的活性催化位点、优异的电荷转移、增强的离子扩散和良好的反应动力学,在电流密度为10 mA cm时过电位低至287 mV,塔菲尔斜率仅为43 mV dec。此外,CoFeO纳米颗粒电极在100 h以上表现出相当可观的长期稳定性,且未检测到活性损失。结果表明,通过简单廉价的制备工艺,使用储量丰富的氧化物材料进行大规模水分解具有广阔的前景。

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