posted on 2022-06-01, 08:04authored byKassie
Nigus Shitaw, Chen-Jui Huang, Sheng-Chiang Yang, Yosef Nikodimos, Nigusu Tiruneh Temesgen, Semaw Kebede Merso, Shi-Kai Jiang, Chia-Hsin Wang, She-Huang Wu, Wei-Nien Su, Bing Joe Hwang
Even
though the anode-free lithium metal battery (AFLMB) is the
next promising energy-storage device because of its high energy density,
the irreversible interfacial phenomena at the Cu/electrolyte interface
are the key failure mechanisms of the AFLMBs. To the best of our knowledge,
the interfacial phenomena associated with the capacity fading of AFLMBs
are not reported yet. Herein, hot cycling combined with electrolyte
formulation using 1% tris(trimethylsilyl) phosphite (TMSP) additive
has been used as a protocol to systematically investigate the Cu/electrolyte
interfacial phenomena of Li nucleation, compactness of deposited Li,
inactive Li (“dead Li” and Li for solid–electrolyte
interphase (SEI) formation “SEI-Li”), electrolyte decomposition,
and SEI layer formation using a scanning electron microscope, scanning
electron microscope-focused ion beam, titration gas chromatography,
in situ gas chromatography–mass spectroscopy, and X-ray photoelectron
spectroscopy, respectively. The synergy of hot cycling and the TMSP
additive lowers the nucleation barrier in Li/Cu from 76.2 to 21.7
mV and increases the compactness of deposited Li from 32.3 to 43.8%
and decreases “dead Li” from 45.18 to 10.86% and SEI-Li
from 31.04 to 12.49% of anode-free Cu/NMC111. Because of the synergy
effects, the Cu/NMC111 cell provides over 100 cycles with an average
coulombic efficiency (avg. CE) of 98.6% for the first 60 cycles and
a capacity retention (CR) of 60.4% at the end of the 60th cycle at
0.2/0.5 mA cm–2 charger/discharge current density,
while the cell with 1 M LiPF6 EC/DEC at 25 °C offers
only an avg. CE of 92.8% for the first 15 cycles with a CR of 40.4%
at the 15th cycle. The results suggest that the synergy of hot cycling
and electrolyte formulation decreases the surface area of deposited
Li and stabilizes the interface that suppresses inventory Li loss.
This work probes the Cu/electrolyte interfacial phenomena, attributed
to the failure mechanisms of AFLMBs. It also sheds light on suitable
strategies to stabilize the Cu interface for stable cycling of AFLMBs.