A high-performance composite ORR catalyst based on the synergy between binary transition metal nitride and nitrogen-doped reduced graphene oxide

被引:96
作者
Dong, Yuanyuan [1 ]
Deng, Yijie [1 ]
Zeng, Jianhuang [1 ]
Song, Huiyu [1 ]
Liao, Shijun [1 ]
机构
[1] South China Univ Technol, Key Lab Fuel Cell Technol Guangdong Prov, Key Lab New Energy Guangdong Univ, Sch Chem & Chem Engn, Guangzhou 510641, Guangdong, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
OXYGEN REDUCTION REACTION; EFFICIENT CATALYST; TITANIUM NITRIDE; RECENT PROGRESS; CARBON; ELECTROCATALYST; LAYERS; NANOELECTROCATALYSTS; NANOMATERIALS;
D O I
10.1039/c6ta10496g
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 a composite catalyst in which binary transition metal nitride nanoparticles (NPs) were mounted on nitrogen-doped reduced graphene oxide (TiCoNx/N-rGO). The catalyst exhibited outstanding oxygen reduction activity in an alkaline medium. In its optimal form, our catalyst yielded a half-wave potential of 0.902 V (vs. RHE), similar to 30 mV more positive than that of the commercial Pt/C catalyst, and its current density at 0.9 V (vs. RHE) reached 2.51 mA cm(-2). The ORR activity of our transition metal nitridemounted N-rGO was much higher than the activities of transition metal nitride alone or N-rGO alone, revealing a strong synergistic effect between the two materials. Further, the catalyst mounted with Ti and Co binary NPs exhibited higher ORR activity than the catalyst mounted solely with Ti nitride NPs, indicating the significant improvement gained by the addition of cobalt. XPS analysis results showed that the mounting of transition metal nitride clearly changed the amount and distribution of N species in the catalyst, causing the percentage of active pyridinic-N species to increase significantly. Moreover, changes in the binding energies of C and Ti atoms proved the synergy between TiCoNx NPs and N-rGO. We therefore ascribe the superior electrochemical activity of our TiCoNx/N-rGO catalyst to this synergy and to the improvement resulting from the addition of Co. In addition to its outstanding ORR activity, this catalyst also showed excellent stability and methanol tolerance, making it a promising Pt-free ORR catalyst for alkaline H-2/O-2 fuel cells and direct methanol fuel cells.
引用
收藏
页码:5829 / 5837
页数:9
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