TY - JOUR
T1 - Hydrated LiOH modified Ni0.1Fe0.9PS3 anodes towards safer high-performance lithium-ion batteries
AU - Lenus, Syama
AU - Yaoda, Liu
AU - Thakur, Pallavi
AU - Lal, Ashique
AU - Samantaray, Sai Smruti
AU - Dai, Zhengfei
AU - Narayanan, Tharanagttu N.
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/4/10
Y1 - 2024/4/10
N2 - Direct contact pre-lithiation with additives in anodes brings a potential strategy for developing highly cyclable lithium ion batteries (LIBs). Herein, using hydrated LiOH as an additive having multifunctional roles, applications of Ni-doped FePS3 (Ni0.1Fe0.9PS3) layers are theoretically and experimentally demonstrated for high capacity and cyclability LIBs. It is shown that the aggregation of Li2S, affecting reversibility of chalcogenide-based anodes while hosting lithium ions in the reversible intercalation process, can be addressed by weakening the bond polarizability in Fe-S bond with LiOH addition. This improves the cyclability and rate retention along with a higher capacity, evincing hydrated LiOH as a safer pre-lithiation agent – unlike many other reported additives. The calculated density of states of pre-lithiated Ni0.1Fe0.9PS3 reveals the development of new symmetric point that is beneficial for achieving high electrical conductivity along with a higher binding energy for Li. The results underline the improved capacity with modification (524 mAh g−1 at 1 A g−1 after 100 cycles) than with that of unmodified one, in tune with the experimental results. This demonstration hence establishes a new safer generic strategy for developing high-rate retention anodes of sulphides in next generation energy storage devices.
AB - Direct contact pre-lithiation with additives in anodes brings a potential strategy for developing highly cyclable lithium ion batteries (LIBs). Herein, using hydrated LiOH as an additive having multifunctional roles, applications of Ni-doped FePS3 (Ni0.1Fe0.9PS3) layers are theoretically and experimentally demonstrated for high capacity and cyclability LIBs. It is shown that the aggregation of Li2S, affecting reversibility of chalcogenide-based anodes while hosting lithium ions in the reversible intercalation process, can be addressed by weakening the bond polarizability in Fe-S bond with LiOH addition. This improves the cyclability and rate retention along with a higher capacity, evincing hydrated LiOH as a safer pre-lithiation agent – unlike many other reported additives. The calculated density of states of pre-lithiated Ni0.1Fe0.9PS3 reveals the development of new symmetric point that is beneficial for achieving high electrical conductivity along with a higher binding energy for Li. The results underline the improved capacity with modification (524 mAh g−1 at 1 A g−1 after 100 cycles) than with that of unmodified one, in tune with the experimental results. This demonstration hence establishes a new safer generic strategy for developing high-rate retention anodes of sulphides in next generation energy storage devices.
KW - Density Functional Theory
KW - High rate retention
KW - Iron phosphorous trichalcogenide
KW - Pre-lithiation
KW - Rechargeable battery
UR - https://www.scopus.com/pages/publications/85186961925
U2 - 10.1016/j.electacta.2024.144010
DO - 10.1016/j.electacta.2024.144010
M3 - 文章
AN - SCOPUS:85186961925
SN - 0013-4686
VL - 483
JO - Electrochimica Acta
JF - Electrochimica Acta
M1 - 144010
ER -