Ionic liquid in-situ functionalized carbon nanotube film as self-supported metal-free electrocatalysts for oxygen evolution

离子液体 析氧 碳纳米管 原位 材料科学 氧气 化学工程 离子键合 纳米技术 金属 电极 催化作用 化学 有机化学 电化学 离子 冶金 物理化学 工程类
作者
Tianhao Li,Yage Wang,Tingting Chen,Guangzhao Wang,Chuntian Qiu,Weihua Hu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:484: 149767-149767 被引量:7
标识
DOI:10.1016/j.cej.2024.149767
摘要

The oxygen evolution reaction (OER) is a critical cathode reaction for hydrogen production from water splitting. However, due to the sluggish kinetics of OER, the water-splitting process is impeded. Thus, it is imperative to develop efficient and low-cost electrocatalysts that reduce the overpotential and improve the kinetics of OER. Herein, an in-situ synthesis strategy was applied to prepare the ionic liquid functionalized carbon nanotube (IL-CNT) that served as a metal-free electrocatalyst for OER. This powder material exhibited exceptional electrocatalytic activity for OER, with an overpotential of 335 mV at 10 mA cm−2 and a Tafel slope of 71 mV dec-1. Then, it was found that catalytic activity was influenced by the IL anion. Moreover, this IL-CNT powder could self-assemble to form carbon film during preparation, exhibiting outstanding catalytic activity for OER (a low overpotential of 153 mV at 10 mA cm−2), which was highly beneficial for practical application. Based on the theoretical calculations and experimental results, these in-situ functionalization sites on CNT surface played a significant role in regulating their electron structure. This, in turn, promoted electron transfer and hydroxyl adsorption, resulting in a substantial increase in catalytic activity for the OER.

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