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通过S掺杂和CeO界面实现具有优化中间结合能的Ni(OH)上的高性能电催化水氧化。

Achieving High-Performance Electrocatalytic Water Oxidation on Ni(OH) with Optimized Intermediate Binding Energy Enabled by S-Doping and CeO -Interfacing.

作者信息

Chen Xiang, Xu Xinyue, Cheng Yuwen, Liu He, Li Dongdong, Da Yumin, Li Yongtao, Liu Dongming, Chen Wei

机构信息

School of Materials Science and Engineering, Anhui University of Technology, Maanshan, 243002, P. R. China.

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore.

出版信息

Small. 2024 Feb;20(8):e2303169. doi: 10.1002/smll.202303169. Epub 2023 Oct 10.

Abstract

The adsorption energy of the reaction intermediates has a crucial influence on the electrocatalytic activity. Ni-based materials possess high oxygen evolution reaction (OER) performance in alkaline, however too strong binding of *OH and high energy barrier of the rate-determining step (RDS) severely limit their OER activity. Herein, a facile strategy is shown to fabricate novel vertical nanorod-like arrays hybrid structure with the interface contact of S-doped Ni(OH) and CeO in situ grown on Ni foam (S-Ni(OH) /CeO /NF) through a one-pot route. The alcohol molecules oxidation reaction experiments and theoretical calculations demonstrate that S-doping and CeO -interfacing significantly modulate the binding energies of OER intermediates toward optimal value and reduce the energy barrier of the RDS, contributing to remarkable OER activity for S-Ni(OH) /CeO /NF with an ultralow overpotential of 196 mV at 10 mA cm and long-term durability over 150 h for the OER. This work offers an efficient doping and interfacing strategy to tune the binding energy of the OER intermediates for obtaining high-performance electrocatalysts.

摘要

反应中间体的吸附能对电催化活性有着至关重要的影响。镍基材料在碱性条件下具有较高的析氧反应(OER)性能,然而,*OH的强吸附以及速率决定步骤(RDS)的高能量势垒严重限制了它们的OER活性。在此,展示了一种简便的策略,通过一锅法原位生长在泡沫镍(S-Ni(OH)₂/CeO₂/NF)上制备具有S掺杂的Ni(OH)₂与CeO₂界面接触的新型垂直纳米棒状阵列杂化结构。醇分子氧化反应实验和理论计算表明,S掺杂和CeO₂界面显著调节了OER中间体的结合能至最佳值,并降低了RDS的能量势垒,使得S-Ni(OH)₂/CeO₂/NF具有显著的OER活性,在10 mA cm⁻²时过电位低至196 mV,且OER的长期耐久性超过150小时。这项工作提供了一种有效的掺杂和界面策略来调节OER中间体的结合能,以获得高性能的电催化剂。

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