An effective strategy for fabricating highly dispersed nanoparticles on O-C3N4 with enhanced electrocatalytic activity and stability

被引:17
作者
Chen, Wei [1 ]
Jiang, Ding [1 ]
Zhu, Mingyue [1 ]
Shi, Tingyan [1 ]
Li, Henan [1 ]
Wang, Kun [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen-doped graphitic carbon nitrogen; Support; Dispersion; Thermal treatment; Oxygen evolution reaction; CARBON NITRIDE FRAMEWORKS; NITROGEN-DOPED GRAPHENE; OXYGEN EVOLUTION; COFE2O4; NANOPARTICLES; GRAPHITIC C3N4; G-C3N4; WATER; PERFORMANCE; REDUCTION; CATALYSTS;
D O I
10.1016/j.jallcom.2018.01.271
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
Uniform distribution of nanoparticles (NPs) with small particle size is hardly controllable, which has an impact on the electrocatalytic properties. In this work, CoFe2O4/oxygen-doped graphitic carbon nitrogen (O-C3N4) was synthesized by glycine-nitrate combustion method, which has many advantages such as high compositional homogeneity and fine particle size. O-C3N4 as a support possessing abundant oxygenated functional groups can provide more active sites for anchoring metal ions, and effectively avoid or minimize the growth and aggregation of CoFe2O4 NPs. As a result, CoFe2O4 NPs with a number-mean particle size of 5.06 +/- 0.42 nm were homogeneously fabricated on the surface of O-C3N4. Moreover, the performance of catalysis was estimated using oxygen evolution reaction (OER) as a model system. The OER performance was remarkably improved including long-term stability and the overpotential of CoFe2O4/O-C3N4 hybrid for 10 mA/cm(2) current densities with a decrease of 131 mV and 61 mV compared with CoFe2O4 and CoFe2O4/graphitic carbon nitrogen (g-C3N4) hybrid, respectively. These indicate that oxygenated functional groups on O-C3N4 not only leads to homogeneous distribution of CoFe2O4 NPs, but also improves the performance for OER. Finally, O-C3N4 could act as a novel support to enhance the dispersion of NPs for the further application in catalysis. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1203 / 1211
页数:9
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