TY - JOUR
T1 - Cobalt nanocrystals embedded into N-doped carbon as highly active bifunctional electrocatalysts from pyrolysis of triazolebenzoate complex
AU - Wei, Zhaojun
AU - Yang, Yang
AU - Liu, Minmin
AU - Dong, Jing
AU - Fan, Xiujun
AU - Zhang, Xian Ming
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/9/10
Y1 - 2018/9/10
N2 - A new and highly-efficient electrocatalyst, constructed by surface enwraped Co nanocrystyals (NCs) embedded into 2-dimensional N-doping graphitized carbon layer (Co@NC), is synthesized by simple one-pot thermal treatment of complex Co(tzbc)2(H2O)4 (tzbc = 4-(1H-1,2,4-triazol-1-yl) benzoate). The utilization of stoichiometrically clear Co(tzbc)2(H2O)4 as precursor could reap following benefits: i) sp2 carbon and nitrogen in tzbc groups could directly convert to N-doping graphitized carbon; ii) metallic Co NCs formed from the thermal reduction of Co2+ in Co(tzbc)2(H2O)4, which can subsequently catalyze the graphitization of the obtained carbons, avoiding additional reducing agent or using potentially dangerous atmosphere; iii) most importantly, complex precursor is easily available and could synthesize in a large scale by simple stirring reaction. As a result, the Co@NC catalyst exhibits excellent activity and stability toward both hydrogen and oxygen evolution reactions (HER and OER, respectively), approaching electrocatalytic performance shown by state-of-the-art Pt and RuO2. Such excellent HER and OER activities are attributed to the synergistic effect of the surface enwraped cobalt nanocrystyals and high conductivity of N-doped graphitized carbon.
AB - A new and highly-efficient electrocatalyst, constructed by surface enwraped Co nanocrystyals (NCs) embedded into 2-dimensional N-doping graphitized carbon layer (Co@NC), is synthesized by simple one-pot thermal treatment of complex Co(tzbc)2(H2O)4 (tzbc = 4-(1H-1,2,4-triazol-1-yl) benzoate). The utilization of stoichiometrically clear Co(tzbc)2(H2O)4 as precursor could reap following benefits: i) sp2 carbon and nitrogen in tzbc groups could directly convert to N-doping graphitized carbon; ii) metallic Co NCs formed from the thermal reduction of Co2+ in Co(tzbc)2(H2O)4, which can subsequently catalyze the graphitization of the obtained carbons, avoiding additional reducing agent or using potentially dangerous atmosphere; iii) most importantly, complex precursor is easily available and could synthesize in a large scale by simple stirring reaction. As a result, the Co@NC catalyst exhibits excellent activity and stability toward both hydrogen and oxygen evolution reactions (HER and OER, respectively), approaching electrocatalytic performance shown by state-of-the-art Pt and RuO2. Such excellent HER and OER activities are attributed to the synergistic effect of the surface enwraped cobalt nanocrystyals and high conductivity of N-doped graphitized carbon.
KW - 0D triazole-benzoate complex (Co-tzbc)
KW - Co@NC
KW - Hydrogen evolution reaction (HER)
KW - Oxygen evolution reaction (OER)
UR - https://www.scopus.com/pages/publications/85050908239
U2 - 10.1016/j.electacta.2018.07.163
DO - 10.1016/j.electacta.2018.07.163
M3 - 文章
AN - SCOPUS:85050908239
SN - 0013-4686
VL - 284
SP - 733
EP - 741
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -