TY - JOUR
T1 - Tin-Based Oxide, Alloy, and Selenide Li-Ion Battery Anodes Derived from a Bimetallic Metal-Organic Material
AU - Foley, Sarah
AU - Geaney, Hugh
AU - Kennedy, Tadhg
AU - Aminu, Ibrahim
AU - Bree, Gerard
AU - McCarthy, Kieran
AU - Darwish, Shaza
AU - Connolly, Sinead
AU - Mukherjee, Soumya
AU - Lebedev, Vasily
AU - Zaworotko, Michael J.
AU - Ryan, Kevin M.
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2021/1/21
Y1 - 2021/1/21
N2 - Here we report the formation of three distinct Sn-based active materials for Li-ion battery anodes, formed from the same metal-organic material (MOM) precursor sql-1-Cu-SNIFSIX. The materials were obtained under three different anneal conditions in air, Ar, and a Se-rich atmosphere, leading to the selective formation of SnO2/CuO/C (oxide), Cu6Sn5/C (stannide), and Cu2SnSe3/SnSe2/C (selenide) composites. The lithiation and delithiation mechanisms were investigated for each material in the potential range of 0-3 V. Over extended cycling periods, the reversible alloying of Li with Sn was the only process evident for the stannide, with minimal activity occurring at potentials greater than 1 V. In contrast to this, the oxide and selenide composites exhibit both conversion (1-3 V) and Li/Sn alloying (0-1 V) behavior in this potential range; however, the stability of the conversion reaction was found to be poor, inhibiting the capacity retention of both materials. Notably, when the reaction mechanisms were restricted to Li/Sn alloying only by limiting the potential range to 0-1 V, all three composite materials significantly outperformed a Sn nanopowder electrode, illustrating the benefits of utilizing composite electrodes to stabilize the Sn alloying reaction over extended cycling periods.
AB - Here we report the formation of three distinct Sn-based active materials for Li-ion battery anodes, formed from the same metal-organic material (MOM) precursor sql-1-Cu-SNIFSIX. The materials were obtained under three different anneal conditions in air, Ar, and a Se-rich atmosphere, leading to the selective formation of SnO2/CuO/C (oxide), Cu6Sn5/C (stannide), and Cu2SnSe3/SnSe2/C (selenide) composites. The lithiation and delithiation mechanisms were investigated for each material in the potential range of 0-3 V. Over extended cycling periods, the reversible alloying of Li with Sn was the only process evident for the stannide, with minimal activity occurring at potentials greater than 1 V. In contrast to this, the oxide and selenide composites exhibit both conversion (1-3 V) and Li/Sn alloying (0-1 V) behavior in this potential range; however, the stability of the conversion reaction was found to be poor, inhibiting the capacity retention of both materials. Notably, when the reaction mechanisms were restricted to Li/Sn alloying only by limiting the potential range to 0-1 V, all three composite materials significantly outperformed a Sn nanopowder electrode, illustrating the benefits of utilizing composite electrodes to stabilize the Sn alloying reaction over extended cycling periods.
UR - http://www.scopus.com/inward/record.url?scp=85099663957&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.0c06395
DO - 10.1021/acs.jpcc.0c06395
M3 - Article
AN - SCOPUS:85099663957
SN - 1932-7447
VL - 125
SP - 1180
EP - 1189
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 2
ER -