Investigating the active sites in molybdenum anchored nitrogen-doped carbon for alkaline oxygen evolution reaction

被引:18
|
作者
Wang, Yuan [1 ]
Dong, Rui [1 ]
Tan, Pengfei [1 ]
Liu, Hongqin [1 ]
Liao, Hanxiao [1 ]
Jiang, Min [1 ]
Liu, Yong [1 ]
Yang, Lu [2 ]
Pan, Jun [1 ]
机构
[1] Cent South Univ, State Key Lab Powder Met, Changsha 410083, Peoples R China
[2] Changsha Univ, Hunan Prov Collaborat Innovat Ctr Environm & Ener, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen evolution reaction; Nitrogen doped carbon materials; Mo-C bonds; Active sites; POROUS CARBON; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; REDUCTION; CATALYSTS; CARBIDE; HETEROSTRUCTURES; NANOPARTICLES; COMPOSITES; BATTERIES;
D O I
10.1016/j.jcis.2021.11.058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing durable and efficient non-precious-metal based catalysts for oxygen evolution reaction (OER) is highly desirable in the field of electrocatalysis. In this work, a series of novel Mo anchored N-doped carbon catalysts (denoted as Mo/NC-T) were prepared starting from the zeolitic imidazolate framework 8 (ZIF-8) precursor. Firstly, Mo doped ZIF-8 precursor (Mo/ZIF-8) with a regular polyhedron structure was formed through a simple ion-exchange method process between molybdenum pentachloride (MoCl5) and ZIF-8. Afterward, Mo/ZIF-8 was converted to Mo/NC-T through a two-step calcination process in nitrogen (N-2) and ammonia (NH3). The as-synthesized Mo/NC-T samples exhibited superior electrocatalytic OER properties. The optimal sample at 650 degrees C (Mo/NC-650) presented a low overpotential of 320 mV at 10 mA cm(-2), a Tafel slope of 71 mV dec(-1), and an outstanding long-term stability for 30 h in 1 M KOH solution. The remarkable OER activity of Mo/NC-T could be ascribed to the structural stability of carbon matrix and the synergistic effect between Mo3+ (derived from Mo-C bonds) and pyridinic N. This work provides a novel perspective on the roles of Mo species in the N-doped carbon electrocatalysts for OER. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:617 / 626
页数:10
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