Cobalt-Embedded Nitrogen-Rich Carbon Nanotubes Efficiently Catalyze Hydrogen Evolution Reaction at All pH Values**

被引:906
作者
Zou, Xiaoxin [1 ,2 ,3 ]
Huang, Xiaoxi [1 ]
Goswami, Anandarup [1 ,2 ]
Silva, Rafael [1 ]
Sathe, Bhaskar R. [1 ,2 ]
Mikmekova, Eliska [4 ]
Asefa, Tewodros [1 ,2 ]
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Chem & Biochem Engn, Piscataway, NJ 08854 USA
[3] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth Preparat Chem, Changchun 130012, Peoples R China
[4] ASCR, Inst Sci Instruments, Vvi, Brno 61264, Czech Republic
基金
美国国家科学基金会;
关键词
carbon nanotubes; cobalt nanoparticles; electrocatalysis; hydrogen evolution reaction; water splitting; ACTIVE EDGE SITES; MOS2 ULTRATHIN NANOSHEETS; OXYGEN REDUCTION; H-2; PRODUCTION; WATER; ELECTROCATALYSTS; IRON; NANOMATERIALS; ELECTRO;
D O I
10.1002/anie.201311111
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite being technically possible, splitting water to generate hydrogen is still practically unfeasible due mainly to the lack of sustainable and efficient catalysts for the half reactions involved. Herein we report the synthesis of cobalt-embedded nitrogen-rich carbon nanotubes (NRCNTs) that 1) can efficiently electrocatalyze the hydrogen evolution reaction (HER) with activities close to that of Pt and 2) function well under acidic, neutral or basic media alike, allowing them to be coupled with the best available oxygen-evolving catalystswhich also play crucial roles in the overall water-splitting reaction. The materials are synthesized by a simple, easily scalable synthetic route involving thermal treatment of Co2+-embedded graphitic carbon nitride derived from inexpensive starting materials (dicyandiamide and CoCl2). The materials' efficient catalytic activity is mainly attributed to their nitrogen dopants and concomitant structural defects.
引用
收藏
页码:4372 / 4376
页数:5
相关论文
共 43 条
[1]  
Andreiadis ES, 2013, NAT CHEM, V5, P48, DOI [10.1038/NCHEM.1481, 10.1038/nchem.1481]
[2]  
[Anonymous], 2012, ANGEW CHEM INT ED, V51, P6131
[3]  
[Anonymous], 2013, ANGEW CHEM INT ED, V52, P371
[4]  
[Anonymous], 2012, ANGEW CHEM INT ED, V51, P12703
[5]  
[Anonymous], 2011, ANGEW CHEM INT ED, V50, P7238
[6]  
Artero V., 2011, ANGEW CHEM, V123, P7376, DOI [DOI 10.1002/ANIE.201007987, DOI 10.1002/ange.201007987]
[7]   Amorphous Molybdenum Sulfide Catalysts for Electrochemical Hydrogen Production: Insights into the Origin of their Catalytic Activity [J].
Benck, Jesse D. ;
Chen, Zhebo ;
Kuritzky, Leah Y. ;
Forman, Arnold J. ;
Jaramillo, Thomas F. .
ACS CATALYSIS, 2012, 2 (09) :1916-1923
[8]   Mixed Close-Packed Cobalt Molybdenum Nitrides as Non-noble Metal Electrocatalysts for the Hydrogen Evolution Reaction [J].
Cao, Bingfei ;
Veith, Gabriel M. ;
Neuefeind, Joerg C. ;
Adzic, Radoslav R. ;
Khalifah, Peter G. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (51) :19186-19192
[9]  
Chen W-F, 2012, ANGEW CHEM, V124, P6235
[10]   Active and stable carbon nanotube/nanoparticle composite electrocatalyst for oxygen reduction [J].
Chung, Hoon T. ;
Won, Jong H. ;
Zelenay, Piotr .
NATURE COMMUNICATIONS, 2013, 4