Silicon (Si) with high specific capacity has received
increasing
attention for rechargeable battery anode materials. However, particle
pulverization as a result of the large volume expansion of Si anodes
further aggravated electrochemical performance degradation during
the process of charging and discharging. In this work, we report the
room-temperature rapid self-healing polymer binders (Al/Alg-TUEG)
synthesized via dynamic coordination bonds (Al–O) and hydrogen
bonds from poly(ether-thioureas) (TUEG). The prepared polymer binders
exhibit a peeling force of 4.2 N, a swelling ratio of 9.5%, and a
recovery of 90% in 2 h at room temperature. As a result, the Si@Al/Alg-TUEG
anodes stably cycle for 300 cycles at 0.5 C with a capacity retention
rate of 77.4%. A high initial Coulombic efficiency (CE) of 87.2% and
good rate performance are also achieved. In terms of full cell performance,
both LiFePO4//Si@Al/Alg-TUEG and NCM811//Si@Al/Alg-TUEG
display stable cycling for 100 cycles at 0.5 C. The capacity retention
of both full cells reaches 93.8 and 92.5%. Good recoverability at
high rates is also found. The superior electrochemical performance
of the Si anode indicates that Al/Alg-TUEG polymer with rapid self-healing
capability at room-temperature is one of the promising binder candidates
for next-generation high-energy-density lithium-ion batteries.