Hollow carbon nanospheres@graphitic C3N5 heterostructures for enhanced oxygen electroreduction

异质结 催化作用 解吸 材料科学 电子转移 密度泛函理论 化学工程 活化能 氧气 化学 纳米技术 光化学 光电子学 物理化学 吸附 计算化学 有机化学 工程类
作者
Qi Li,Shizhu Song,Zhiyong Mo,Lifang Zhang,Yijun Qian,Cunwang Ge
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:579: 152006-152006 被引量:26
标识
DOI:10.1016/j.apsusc.2021.152006
摘要

Improving the electrocatalytic activity of metal-free catalysts for the oxygen reduction reaction (ORR) is of great significance as promising alternatives to the Pt group precious catalysts in fuel cells. This paper proposes a simple template-based strategy to fabricate a catalyst with enhanced ORR activity. The resulting material contained 3D heterojunction and consisted of hollow carbon nanospheres and graphitic C3N5 ([email protected]3N5). The fast electron/charge transports between g-C3N5 and HCNs was achieved because of the conductive heterojunction presence. This heterojunction provided the potential difference, which is beneficial for O2 activation and desorption of the intermediate reaction products. Compared with stand-alone HCNs and g-C3N5, the [email protected]3N5 composite demonstrated significantly enhanced ORR activity with a more positive half-wave potential and faster kinetics in the alkaline medium. Furthermore, linear sweep voltammetry demonstrated that the water generation from O2 occurred through a four-electron transfer reaction. According to calculations performed using density functional theory (DFT), a built-in electronic field (IEF) formed at the heterojunction because of the charge density difference between C and N atoms. This IEF reduced the O2 activation energy and lowered the charge transfer resistance, which, in turn, enabled the rapid formation and desorption of the intermediates and significantly enhanced ORR activity of [email protected]3N5.
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