posted on 2024-10-23, 15:35authored byWei Bai, Fudong Zhao, Zhirong Wang, Junling Wang, Richard K. K. Yuen, Xiaoxi Zheng
Nowadays,
the extended usage of lithium/sodium ion batteries (LIBs/SIBs)
encounters nerve-wracking issues, including a lack of suitable reservoirs
and high thermal runaway hazards. Although using TiO2 and
Li4Ti5O12 has been confirmed to be
effective in improving battery safety, their low theoretical capacities
inevitably cause damage to the electrochemical performance of the
battery. Achieving win-win results has become an urgent necessity.
This study designed a metal–organic framework (MOF)-derived
in situ carbon-coated metal selenide (Ni–Se@G@C) as the anode.
When the current density is 0.1–0.3 A g–1, the initial capacity of LIBs reaches 993.2 mAh g–1, which increases to 1478.9 mAh g–1 after running
800 cycles. When running at 2 A g–1, the cell also
offers a relatively high capacity of 458.3 mAh g–1 after 1500 cycles. After the replacement of graphite with Ni–Se@G@C,
the self-heating temperature (T0) and
thermal runaway triggering temperature (T1) of half and full cells are significantly increased. Meanwhile,
the maximum thermal runaway temperature (T2) and maximal heating release rate (HRRmax) are significantly
reduced. Of note, the usage of Ni–Se@G@C enables the battery
with superior cycling and rate performance. When used in SIBs, the
cell gives an initial discharge capacity of 624.9 mAh g–1, which still remains at 269.4 mAh g–1 after running
200 cycles at 1 A g–1. Notably, Ea of the Ni–Se@G@C cell is 5.6 times higher than
that of the graphite cell, corroborating the promoted safety performance.
This work provides a new paradigm for MOF-derived micro/nanostructures,
enabling the battery with an excellent electrochemical and safety
performance portfolio.