Boron-doped graphene as promising support for platinum catalyst with superior activity towards the methanol electrooxidation reaction

被引:77
作者
Sun, Yongrong [1 ]
Du, Chunyu [1 ]
An, Meichen [1 ]
Du, Lei [1 ]
Tan, Qiang [1 ]
Liu, Chuntao [2 ]
Gao, Yunzhi [1 ]
Yin, Geping [1 ]
机构
[1] Harbin Inst Technol, Inst Adv Chem Power Sources, Sch Chem Engn & Technol, Harbin 150001, Peoples R China
[2] Heilongjiang Univ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China
基金
美国国家科学基金会;
关键词
Boron doped graphene; Platinum catalyst support; Methanol electrooxidation; Carbon monoxide tolerance; Stability; ELECTROCATALYTIC ACTIVITY; OXYGEN REDUCTION; CATHODE CATALYST; CARBON; OXIDATION; NANOPARTICLES; MICROWAVE; EFFICIENT; PERFORMANCE; ELECTRODE;
D O I
10.1016/j.jpowsour.2015.09.046
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
We report the synthesis of boron-doped graphene by thermally annealing the mixture of graphene oxide and boric acid, and its usage as the support of Pt catalyst towards the methanol oxidation reaction. The composition, structure and morphology of boron-doped graphene and its supported Pt nanoparticles (Pt/BC) are characterized by transmission electron microscopy, inductively coupled plasma mass spectrometry, Raman spectroscopy, X-ray diffraction and X-ray photoelectron spectroscopy. It is revealed that boron atoms are doped into graphene network in the form of BC2O and BCO2 bonds, which lead to the increase in defect sites and facilitate the subsequent deposition of Pt nanoparticles. Therefore, the Pt/BC catalyst presents smaller particle size and narrower size distribution than the graphene supported Pt (Pt/G) catalyst. When evaluated as the electrocatalyst for the methanol oxidation reaction, the Pt/BG catalyst exhibits excellent electrochemical activity and stability demonstrated by cyclic voltammetry and chronoamperometry tests. The enhanced activity is mainly ascribed to the electronic interaction between boron-doped graphene and Pt nanoparticles, which lowers the d-band center of Pt and thus weakens the absorption of the poisoning intermediate CO. Our work provides an alternative approach of improving the reaction kinetics for the oxidation of small organic molecules. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 253
页数:9
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