TY - JOUR
T1 - The effects of Ni on inhibiting the separation of Cu during the lithiation of Cu6Sn5 lithium-ion battery anodes
AU - Tan, Xin F.
AU - McDonald, Stuart D.
AU - Gu, Qinfen
AU - Wang, Lianzhou
AU - Matsumura, Syo
AU - Nogita, Kazuhiro
N1 - Funding Information:
This work was supported by the UQ-Nihon Superior cooperative research grant [ 2016001895 ] at the University of Queensland (UQ), Australia ; an Australian Government Research Training Program (RTP) grant from the University of Queensland, Australia ; the Nanotechnology Platform project [ A-17-KU-225 ] for advanced nanostructure characterisation from Kyushu University (KU), Japan ; the Progress 100 program at Kyushu University, Japan ; and a “UQ-KU project” at the University of Queensland, Australia , which assists research collaborations between UQ and KU.
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/11/15
Y1 - 2019/11/15
N2 - Sn-based lithium-ion battery (LIB) anodes have a lower risk of lithium dendrite formation and a higher storage capacity of 993 mAh g−1 vs. 372 mAh g−1 compared to carbon-based anodes. Alloying Sn with Cu can reduce the reaction stresses in the anode, and Cu6Sn5 is therefore a promising candidate material to replace carbon-based anodes. However, the separation of Cu during the second stage of the lithiation reaction results in slow kinetics and degrades the cyclability of the anodes. This study proposes an effective method to inhibit the separation of Cu via the addition of Ni. Ni occupies the Cu positions in the Cu6Sn5 crystal structures to form (Cu, Ni)6Sn5, and therefore alters the crystal structure of the anode, leading to the formation of superstructures. As a result, Ni partially blocks the diffusion pathways of Li and therefore inhibits the Cu separation reaction, while the superstructure provides additional Li storage sites to increase the capacity of the anodes. Ni also refines the grain size of Cu6Sn5, leading to faster kinetics. The reaction mechanisms of the modified anodes are confirmed by in-situ synchrotron X-ray powder diffraction and ex-situ high voltage transmission electron microscopy.
AB - Sn-based lithium-ion battery (LIB) anodes have a lower risk of lithium dendrite formation and a higher storage capacity of 993 mAh g−1 vs. 372 mAh g−1 compared to carbon-based anodes. Alloying Sn with Cu can reduce the reaction stresses in the anode, and Cu6Sn5 is therefore a promising candidate material to replace carbon-based anodes. However, the separation of Cu during the second stage of the lithiation reaction results in slow kinetics and degrades the cyclability of the anodes. This study proposes an effective method to inhibit the separation of Cu via the addition of Ni. Ni occupies the Cu positions in the Cu6Sn5 crystal structures to form (Cu, Ni)6Sn5, and therefore alters the crystal structure of the anode, leading to the formation of superstructures. As a result, Ni partially blocks the diffusion pathways of Li and therefore inhibits the Cu separation reaction, while the superstructure provides additional Li storage sites to increase the capacity of the anodes. Ni also refines the grain size of Cu6Sn5, leading to faster kinetics. The reaction mechanisms of the modified anodes are confirmed by in-situ synchrotron X-ray powder diffraction and ex-situ high voltage transmission electron microscopy.
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U2 - 10.1016/j.jpowsour.2019.227085
DO - 10.1016/j.jpowsour.2019.227085
M3 - Article
AN - SCOPUS:85072157046
SN - 0378-7753
VL - 440
JO - Journal of Power Sources
JF - Journal of Power Sources
M1 - 227085
ER -