TY - JOUR
T1 - New Suggestion of Highly Durable Electrode Design for Ordered Mesoporous Ni–Mn Binary Transition Metal Oxide Anode Material in Lithium-Ion Batteries
AU - Kim, Taewhan
AU - Kim, Kyoung Ho
AU - Kim, Hansol
AU - Lee, Wontae
AU - Choi, Woosung
AU - Yoon, Jaesang
AU - Song, Lianghao
AU - Kim, Ki Jae
AU - Bulakhe, Ravindra N.
AU - Yoon, Won Sub
AU - Kim, Ji Man
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2025/2/5
Y1 - 2025/2/5
N2 - Anode materials storing large-scale lithium ions gradually decrease electrochemical performance due to severe volume changes during cycling. Therefore, there is an urgent need to develop anode materials with high electrochemical capacity and durability, without deterioration arising due to the volume changes during the electrochemical processes. To date, mesoporous materials have received attention as anode materials due to their ability to mitigate volume expansion, offer a short pathway for Li+ transport, and exhibit anomalous high capacity. However, the nano-frameworks of transition metal oxide collapse during conversion reactions, demanding an improvement in nano-framework structure stability. In this study, ordered mesoporous nickel manganese oxide (m-NMO) is designed as an anode material with a highly durable nanostructure. Interestingly, m-NMO showed better cycle performance and higher electrochemical capacity than those of nickel oxide and manganese oxide. Operando small-angle X-ray scattering and ex situ transmission electron microscopic results confirmed that the binary m-NMO sustained a highly durable nanostructure upon cycling, unlike the single metal oxide electrodes where the mesostructures collapsed. Ex situ X-ray absorption spectroscopy proved that nickel and manganese showed different electrochemical reaction voltages, and thus undergoes sequential conversion reactions. As a result, both elements can act as complementary nano-propping buffers to maintain stable mesostructure.
AB - Anode materials storing large-scale lithium ions gradually decrease electrochemical performance due to severe volume changes during cycling. Therefore, there is an urgent need to develop anode materials with high electrochemical capacity and durability, without deterioration arising due to the volume changes during the electrochemical processes. To date, mesoporous materials have received attention as anode materials due to their ability to mitigate volume expansion, offer a short pathway for Li+ transport, and exhibit anomalous high capacity. However, the nano-frameworks of transition metal oxide collapse during conversion reactions, demanding an improvement in nano-framework structure stability. In this study, ordered mesoporous nickel manganese oxide (m-NMO) is designed as an anode material with a highly durable nanostructure. Interestingly, m-NMO showed better cycle performance and higher electrochemical capacity than those of nickel oxide and manganese oxide. Operando small-angle X-ray scattering and ex situ transmission electron microscopic results confirmed that the binary m-NMO sustained a highly durable nanostructure upon cycling, unlike the single metal oxide electrodes where the mesostructures collapsed. Ex situ X-ray absorption spectroscopy proved that nickel and manganese showed different electrochemical reaction voltages, and thus undergoes sequential conversion reactions. As a result, both elements can act as complementary nano-propping buffers to maintain stable mesostructure.
KW - Li-ion battery
KW - binary transition metal oxides
KW - nano-structural durability
KW - ordered mesoporous anode
KW - sequential conversion reaction
UR - http://www.scopus.com/inward/record.url?scp=85205440826&partnerID=8YFLogxK
U2 - 10.1002/smll.202406243
DO - 10.1002/smll.202406243
M3 - Article
C2 - 39363796
AN - SCOPUS:85205440826
SN - 1613-6810
VL - 21
JO - Small
JF - Small
IS - 5
M1 - 2406243
ER -