Bottom-up synthesis of high-performance nitrogen-enriched transition metal/graphene oxygen reduction electrocatalysts both in alkaline and acidic solution

被引:29
作者
Lai, Qingxue [1 ]
Gao, Qingwen [1 ]
Su, Qi [1 ]
Liang, Yanyu [1 ]
Wang, Yuxi [2 ]
Yang, Zhi [2 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Jiangsu, Peoples R China
[2] Shanghai Jiao Tong Univ, Key Lab Thin Film & Microfabricat, Dept Micro Nano Elect, Sch Elect Informat & Elect Engn,Minist Educ, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCHEMICAL ENERGY-STORAGE; FE/N/C-CATALYSTS; METAL-CATALYSTS; NANOSTRUCTURED CARBON; DOPED GRAPHENE; CONVERSION; IRON; NANOMATERIALS; POLYANILINE; DENSITY;
D O I
10.1039/c5nr02984h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxygen reduction electrocatalysts with low cost and excellent performance are urgently required for large-scale application in fuel cells and metal-air batteries. Though nitrogen-enriched transition metal/graphene hybrids (N-TM/G, TM = Fe, Co, and Ni and related compounds) have been developed as novel substitutes for precious metal catalysts (PMCs) towards oxygen reduction reaction (ORR), a significant challenge still remains for simple and efficient synthesis of N-TM/G catalysts with satisfactory electrocatalytic behavior. Herein, we demonstrate a universal bottom-up strategy for efficient fabrication of strongly-coupled N-TM/G catalysts. This strategy is implemented via direct polymerization of transition metal phthalocyanine (TMPc) in the two-dimensional confined space of in situ generated g-C3N4 and a subsequent pyrolysis. Such a space-confined bottom-up synthesis route successfully constructs a strongly-coupled triple junction of transition metal-graphitic carbon-nitrogen-doped graphene (TM-GC-NG) with extensive controllability over the specific surface area, nitrogen content/types as well as the states of metal. As a result, the optimized N-Fe/G materials have promising potential as high-performance NPMCs towards ORR both in alkaline and acidic solution.
引用
收藏
页码:14707 / 14714
页数:8
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