TY - JOUR
T1 - Nanosheet-structured NiCoO2/carbon nanotubes hybrid composite as a novel bifunctional oxygen electrocatalyst
AU - Ma, Li
AU - Zhou, Han
AU - Sun, Yao
AU - Xin, Shuli
AU - Xiao, Chunhui
AU - Kumatani, Akichika
AU - Matsue, Tomokazu
AU - Zhang, Penghui
AU - Ding, Shujiang
AU - Li, Fei
N1 - Funding Information:
This work was financially supported by the National Natural Science Foundation of China ( 21105079 , 51273158 , 21405119 ), the Scientific Research Foundation for the Returned Overseas Chinese Scholars by the State Education Ministry of China , the International Science and Technology Cooperation and Exchange Program of Shaanxi Province of China ( 2016KW-064 ), the Fundamental Research Funds for the Central Universities of China , the General Financial Grant from the China Postdoctoral Science Foundation ( 2016M592773 ), the Chinese Government Scholarship ( 201506285022 ) and the Japan Society for the Promotion of Science (KAKENHI: 16H06042 ).
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/10/20
Y1 - 2017/10/20
N2 - Synthesis of novel bifunctional catalysts based on earth-abundant elements with high catalytic activities for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) becomes a main strategy to promote the development of metal-air batteries and fuel cells. Herein, a novel Co2+-based mixed transition metal oxide composite, the three-dimensional (3D) nanosheet-structured NiCoO2/carbon nanotubes (CNTs) composite, was successfully synthesized through a facile one-pot method. The better electrocatalytic activities of NiCoO2/CNTs for both ORR and OER than those of pure NiCoO2, CNTs, physically mixed NiCoO2 and CNTs, and Co3O4/CNTs are proved. The comparison of local ORR and OER electrocatalytic activities of NiCoO2/CNTs to other catalysts are obtained by scanning electrochemical microscopy (SECM) characterizations. The closed oxygen reduction peak and half-wave potentials, nearly four-electron dominated process, better methanol tolerance and electrochemical stability confirm the comparable electrocatalytic performance and better stability of NiCoO2/CNTs to the commercial Pt/C catalyst for ORR. The similar stability of NiCoO2/CNTs demonstrates its comparable electrocatalytic performance to the state-of-the-art RuO2 catalyst for OER. The as-prepared NiCoO2/CNTs composite presents as a promising bifunctional oxygen electrocatalyst in alkaline solution for potential applications.
AB - Synthesis of novel bifunctional catalysts based on earth-abundant elements with high catalytic activities for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) becomes a main strategy to promote the development of metal-air batteries and fuel cells. Herein, a novel Co2+-based mixed transition metal oxide composite, the three-dimensional (3D) nanosheet-structured NiCoO2/carbon nanotubes (CNTs) composite, was successfully synthesized through a facile one-pot method. The better electrocatalytic activities of NiCoO2/CNTs for both ORR and OER than those of pure NiCoO2, CNTs, physically mixed NiCoO2 and CNTs, and Co3O4/CNTs are proved. The comparison of local ORR and OER electrocatalytic activities of NiCoO2/CNTs to other catalysts are obtained by scanning electrochemical microscopy (SECM) characterizations. The closed oxygen reduction peak and half-wave potentials, nearly four-electron dominated process, better methanol tolerance and electrochemical stability confirm the comparable electrocatalytic performance and better stability of NiCoO2/CNTs to the commercial Pt/C catalyst for ORR. The similar stability of NiCoO2/CNTs demonstrates its comparable electrocatalytic performance to the state-of-the-art RuO2 catalyst for OER. The as-prepared NiCoO2/CNTs composite presents as a promising bifunctional oxygen electrocatalyst in alkaline solution for potential applications.
KW - Nanosheet structure
KW - NiCoO/carbon nanotubes composite
KW - Oxygen evolution reaction
KW - Oxygen reduction reaction
KW - Scanning electrochemical microscopy (SECM)
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U2 - 10.1016/j.electacta.2017.08.192
DO - 10.1016/j.electacta.2017.08.192
M3 - Article
AN - SCOPUS:85028998548
SN - 0013-4686
VL - 252
SP - 338
EP - 349
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -