TY - JOUR
T1 - Suppression of CO2 induced lithium anode corrosion by fluorinated functional group in quasi-solid polymer electrolyte enabling long-cycle and high-safety Li-CO2 batteries
AU - Liu, Limin
AU - Qin, Yanyang
AU - Zhao, Hongyang
AU - Gao, Yiyang
AU - Wang, Ke
AU - Ali, Wajid
AU - Yu, Wei
AU - Zhang, Dongyang
AU - Hu, Xiaofei
AU - Su, Yaqiong
AU - Ding, Shujiang
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/3
Y1 - 2023/3
N2 - Given high theoretical energy density and environmental-friendly CO2 fixation ability, rechargeable Li-CO2 battery is explored as a promising energy storage device. However, its cycling stability and safety are challenged by the continuous pulverization of Li anode and the leakage of liquid electrolytes (LEs). Herein, a quasi-solid polymer electrolyte (QSPE) with -CF3 functional groups was designed and in-situ fabricated for Li-CO2 battery. The solidification of electrolyte avoids the leakage of LEs and effectively inhibits the diffusion of the acid CO2 and cathode by-products to etch Li anode. Besides, the introduction of -CF3 can construct a fish scale-like LiF-rich solid electrolyte interface on Li anode, which induces the uniform and dense deposition of Li to inhibit the deeper Li from being further etched. The QSPE also exhibits high ion conductivity (1.98×10−3 S cm−1 at 25 °C), enhanced Li+ transport number (0.47), and superb stability (>5.27 V vs. Li/Li+). Consequently, the Li-CO2 battery with QSPE delivers effectively suppressed pulverization of Li anode, extraordinary cyclic stability over 295 cycles (1250 h) at 50 μA cm−2, and lower overpotential (1.05 V) compared to the cells with LE. Moreover, the as-prepared QSPE also demonstrates excellent application potential in other Li metal batteries and flexible electronic devices.
AB - Given high theoretical energy density and environmental-friendly CO2 fixation ability, rechargeable Li-CO2 battery is explored as a promising energy storage device. However, its cycling stability and safety are challenged by the continuous pulverization of Li anode and the leakage of liquid electrolytes (LEs). Herein, a quasi-solid polymer electrolyte (QSPE) with -CF3 functional groups was designed and in-situ fabricated for Li-CO2 battery. The solidification of electrolyte avoids the leakage of LEs and effectively inhibits the diffusion of the acid CO2 and cathode by-products to etch Li anode. Besides, the introduction of -CF3 can construct a fish scale-like LiF-rich solid electrolyte interface on Li anode, which induces the uniform and dense deposition of Li to inhibit the deeper Li from being further etched. The QSPE also exhibits high ion conductivity (1.98×10−3 S cm−1 at 25 °C), enhanced Li+ transport number (0.47), and superb stability (>5.27 V vs. Li/Li+). Consequently, the Li-CO2 battery with QSPE delivers effectively suppressed pulverization of Li anode, extraordinary cyclic stability over 295 cycles (1250 h) at 50 μA cm−2, and lower overpotential (1.05 V) compared to the cells with LE. Moreover, the as-prepared QSPE also demonstrates excellent application potential in other Li metal batteries and flexible electronic devices.
KW - In-situ polymerization
KW - Li anode
KW - Li-CO battery
KW - Quasi-solid polymer electrolyte
UR - http://www.scopus.com/inward/record.url?scp=85148545596&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2023.02.006
DO - 10.1016/j.ensm.2023.02.006
M3 - 文章
AN - SCOPUS:85148545596
SN - 2405-8297
VL - 57
SP - 260
EP - 268
JO - Energy Storage Materials
JF - Energy Storage Materials
ER -