TY - JOUR
T1 - A self-supported metal-organic framework derived Co3O4 film prepared by an in-situ electrochemically assistant process as Li ion battery anodes
AU - Zhao, Guangyu
AU - Sun, Xin
AU - Zhang, Li
AU - Chen, Xuan
AU - Mao, Yachun
AU - Sun, Kening
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/6/15
Y1 - 2018/6/15
N2 - Derivates of metal-organic frameworks are promising materials of self-supported Li ion battery anodes due to the good dispersion of active materials, conductive scaffold, and mass transport channels in them. However, the discontinuous growth and poor adherence of metal-organic framework films on substrates hamper their development in self-supported electrodes. In the present study, cobalt-based metal-organic frameworks are anchored on Ti nanowire arrays through an electrochemically assistant method, and then the metal-organic framework films are pyrolyzed to carbon-containing, porous, self-supported anodes of Li ion battery anodes. Scanning electron microscope images indicate that, a layer cobaltosic oxide polyhedrons inserted by the nanowires are obtained with the controllable in-situ synthesis. Thanks to the good dispersion and adherence of cobaltosic oxide polyhedrons on Ti substrates, the self-supported anodes exhibit remarkable rate capability and durability. They possess a capacity of 300 mAh g−1 at a rate current of 20 A g−1, and maintain 2000 charge/discharge cycles without obvious decay.
AB - Derivates of metal-organic frameworks are promising materials of self-supported Li ion battery anodes due to the good dispersion of active materials, conductive scaffold, and mass transport channels in them. However, the discontinuous growth and poor adherence of metal-organic framework films on substrates hamper their development in self-supported electrodes. In the present study, cobalt-based metal-organic frameworks are anchored on Ti nanowire arrays through an electrochemically assistant method, and then the metal-organic framework films are pyrolyzed to carbon-containing, porous, self-supported anodes of Li ion battery anodes. Scanning electron microscope images indicate that, a layer cobaltosic oxide polyhedrons inserted by the nanowires are obtained with the controllable in-situ synthesis. Thanks to the good dispersion and adherence of cobaltosic oxide polyhedrons on Ti substrates, the self-supported anodes exhibit remarkable rate capability and durability. They possess a capacity of 300 mAh g−1 at a rate current of 20 A g−1, and maintain 2000 charge/discharge cycles without obvious decay.
KW - Durability
KW - Electrochemical synthesis
KW - Lithium ion battery
KW - Metal-organic framework
KW - Self-supported anode
UR - http://www.scopus.com/inward/record.url?scp=85044977585&partnerID=8YFLogxK
U2 - 10.1016/j.jpowsour.2018.04.001
DO - 10.1016/j.jpowsour.2018.04.001
M3 - Article
AN - SCOPUS:85044977585
SN - 0378-7753
VL - 389
SP - 8
EP - 12
JO - Journal of Power Sources
JF - Journal of Power Sources
ER -