Hollow-structured CoP nanotubes wrapped by N-doped carbon layer with interfacial charges polarization for efficiently boosting oxygen reduction/evolution reactions

极化(电化学) 氧气 Boosting(机器学习) 化学工程 材料科学 碳纳米管 纳米技术 图层(电子) 氧还原 化学 兴奋剂 电化学 氧还原反应 光电子学 有机化学 物理化学 电极 工程类 机器学习 计算机科学
作者
Bin Liu,Rongyue Wang,Yuan Yao,Jingling Ma,Yubo Sun,Jiafeng Wan,Ying Zhang,Siqi Wang,Jinlong Zou
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:431: 133238-133238 被引量:12
标识
DOI:10.1016/j.cej.2021.133238
摘要

• 1D hollow CoP nanotubes wrapped by NCL are used as efficient catalysts for ORR/OER. • The well-formed 1D hollow structure can exposure more active sites for mass transfer. • CoP/CoOOH heterostructure on CoP-HNTs surface as the main active-species for OER. • Charge redistribution at the CoP/NCL interface promotes both ORR and OER processes. • Graphene layer protects CoP-HNTs@NCL from aggregation and corrosion during ORR/OER. Structure engineering for electrocatalysts via interfacial charge redistribution plays a vital role in governing the electrocatalytic activity for both oxygen reduction and evolution reactions (ORR/OER). Herein, a hierarchical nanostructure consisting of one-dimension (1D) hollow CoP nanotubes wrapped by nitrogen-doped carbon layer (CoP-HNTs@NCL) is designed through a simple hydrothermal-phosphorization-annealing strategy. Morphology of CoP-HNTs@NCL-0.4 (mass ratio of GO to CoP is 0.4) shows that the exterior surface of hollow CoP-HNTs is firmly coated by NCL with a layer thickness of 5-8 nm. ΔE (E j10 (1.58 V, OER)-E 1/2 (0.91 V, ORR)) of CoP-HNTs@NCL-0.4 is as low as 0.67 V for ORR/OER, which outperforms commercial Pt/C and RuO 2 and ranks the top of nonprecious-metal catalysts. Excellent activity and stability of CoP-HNTs@NCL-0.4 for ORR/OER benefit from synergistic effects between CoP and NCL, enhanced mass transfer via 1D hollow structure, and abundant active sites exposed on the interior/exterior surfaces of nanotube wall. Density functional theory calculations confirm that strong coupling interactions lead to interfacial charge polarization to remarkably promote the ORR/OER activities. This study highlights the functions of 1D hollow structure and interface effects in oxygen electrocatalysis, and opens a new avenue for interface construction by synergistically integrating favorable thermodynamics with efficient kinetics through modification of electronic structure.

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