TY - JOUR
T1 - Fabrication of an MOF-derived heteroatom-doped Co/CoO/carbon hybrid with superior sodium storage performance for sodium-ion batteries
AU - Kaneti, Yusuf Valentino
AU - Zhang, Jun
AU - He, Yan Bing
AU - Wang, Zhijie
AU - Tanaka, Shunsuke
AU - Hossain, Md Shahriar A.
AU - Pan, Zheng Ze
AU - Xiang, Bin
AU - Yang, Quan Hong
AU - Yamauchi, Yusuke
N1 - Funding Information:
This project was supported by the National Key Basic Research Program of China (2014CB932400), Youth research funds of Graduate School at Shenzhen, Tsinghua University (QN20150002), and Production-study-research cooperation project of Guangdong province (2014B090901021) and Dongguan City (2015509119213), Shenzhen Basic Research Project (ZDSYS20140509172959981 and KQJSCX20160226191136). Y. V. Kaneti thanks the Japan Society for Promotion of Science (JSPS) and the Australian Government/Cheung Kong Holdings Group for providing the JSPS Standard Postdoctoral Fellowship and the Endeavour Cheung Kong Postdoctoral Fellowship, respectively. The authors thank Mr Chong Luo and Profab for the assistance with the Raman measurement and the sample preparation, respectively.
Publisher Copyright:
© 2017 The Royal Society of Chemistry.
PY - 2017
Y1 - 2017
N2 - Metal-organic frameworks (MOFs) have gained significant attention as precursors for the fabrication of porous hybrid materials due to their highly controllable composition, structure and pore size. However, at present, MOF-derived materials have rarely been investigated as anode materials for sodium-ion batteries. In this work, we report the fabrication of a Ni-doped Co/CoO/N-doped carbon (NC) hybrid using bimetallic Ni-Co-ZIF as the starting precursor. The resulting Ni-doped Co/CoO/NC hybrid is highly microporous with a high specific surface area of 552 m2 g-1. When employed as an anode material for sodium-ion batteries, the Ni-doped Co/CoO/NC hybrid exhibited both good rate performance with a high discharge capacity of 218 mA h g-1 at a high current density of 500 mA g-1 and good cycling stability, as a high discharge capacity of 218.7 mA h g-1 can be retained after 100 cycles at 500 mA g-1, corresponding to a high capacity retention of 87.5%. The excellent electrochemical performance of the Ni-doped Co/CoO/NC hybrid for SIBs may be attributed to the synergistic effects of various factors, including: (i) the presence of a carbon matrix which provides protection against aggregation and pulverization during sodiation/desodiation; (ii) the highly microporous nature along with the presence of a few mesopores which facilitates better insertion/de-insertion of Na+ ions; (iii) the Ni-doping which introduces defect sites into the atomic structure of CoO via partial substitution, thus enhancing the conductivity of the cobalt oxide (CoO) component and hence, the overall hybrid material, and (iv) the N-doping which promotes a faster migration speed of sodium ions (Na+) across the carbon layer by creating defect sites, thereby improving the conductivity of the carbon frameworks in the hybrid material.
AB - Metal-organic frameworks (MOFs) have gained significant attention as precursors for the fabrication of porous hybrid materials due to their highly controllable composition, structure and pore size. However, at present, MOF-derived materials have rarely been investigated as anode materials for sodium-ion batteries. In this work, we report the fabrication of a Ni-doped Co/CoO/N-doped carbon (NC) hybrid using bimetallic Ni-Co-ZIF as the starting precursor. The resulting Ni-doped Co/CoO/NC hybrid is highly microporous with a high specific surface area of 552 m2 g-1. When employed as an anode material for sodium-ion batteries, the Ni-doped Co/CoO/NC hybrid exhibited both good rate performance with a high discharge capacity of 218 mA h g-1 at a high current density of 500 mA g-1 and good cycling stability, as a high discharge capacity of 218.7 mA h g-1 can be retained after 100 cycles at 500 mA g-1, corresponding to a high capacity retention of 87.5%. The excellent electrochemical performance of the Ni-doped Co/CoO/NC hybrid for SIBs may be attributed to the synergistic effects of various factors, including: (i) the presence of a carbon matrix which provides protection against aggregation and pulverization during sodiation/desodiation; (ii) the highly microporous nature along with the presence of a few mesopores which facilitates better insertion/de-insertion of Na+ ions; (iii) the Ni-doping which introduces defect sites into the atomic structure of CoO via partial substitution, thus enhancing the conductivity of the cobalt oxide (CoO) component and hence, the overall hybrid material, and (iv) the N-doping which promotes a faster migration speed of sodium ions (Na+) across the carbon layer by creating defect sites, thereby improving the conductivity of the carbon frameworks in the hybrid material.
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U2 - 10.1039/c7ta03939e
DO - 10.1039/c7ta03939e
M3 - Article
AN - SCOPUS:85026211089
SN - 2050-7488
VL - 5
SP - 15356
EP - 15366
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 29
ER -