TY - JOUR
T1 - A soluble phenolic mediator contributing to enhanced discharge capacity and low charge overpotential for lithium-oxygen batteries
AU - Yu, Wei
AU - Yang, Wei
AU - Liu, Ruliang
AU - Qin, Lei
AU - Lei, Yu
AU - Liu, Liang
AU - Zhai, Dengyun
AU - Li, Baohua
AU - Kang, Feiyu
N1 - Funding Information:
This work was supported by the National Key Basic Research Program of China (Grant No. 2014CB932400) and the National Natural Science Foundation of China (Grant No. 51232005).
Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - In this study, a phenolic antioxidant of 2,6-di-tert-butyl-hydroxytoluene (BHT) is applied in Li-O2 batteries to simultaneously improve discharge capacity and reduce charge overpotential. BHT exhibits a redox couple at ~ 3.0 V (vs. Li+/Li), which is extremely close to the thermodynamic potential of a Li-O2 battery (2.96 V). The unique chemical and electrochemical behaviors of BHT contribute to the improvement on both oxygen reduction reaction and oxygen evolution reaction performances. These factors lead to the notable enhancement of discharge capacity (capacity increases by 72%) and the reduction of charge plateau (the plateau is 3.2 V and 4.2 V, respectively, with and without BHT) for Li-O2 batteries. Furthermore, in-situ X-ray diffraction results confirm that the BHT-mediated formation and decomposition of Li2O2, rather than parasitic reactions, dominate the discharge and charge processes. The results provide a new approach for exploiting appropriate soluble mediators for rechargeable Li-O2 batteries.
AB - In this study, a phenolic antioxidant of 2,6-di-tert-butyl-hydroxytoluene (BHT) is applied in Li-O2 batteries to simultaneously improve discharge capacity and reduce charge overpotential. BHT exhibits a redox couple at ~ 3.0 V (vs. Li+/Li), which is extremely close to the thermodynamic potential of a Li-O2 battery (2.96 V). The unique chemical and electrochemical behaviors of BHT contribute to the improvement on both oxygen reduction reaction and oxygen evolution reaction performances. These factors lead to the notable enhancement of discharge capacity (capacity increases by 72%) and the reduction of charge plateau (the plateau is 3.2 V and 4.2 V, respectively, with and without BHT) for Li-O2 batteries. Furthermore, in-situ X-ray diffraction results confirm that the BHT-mediated formation and decomposition of Li2O2, rather than parasitic reactions, dominate the discharge and charge processes. The results provide a new approach for exploiting appropriate soluble mediators for rechargeable Li-O2 batteries.
KW - Bifunctional mediator
KW - In-situ X-ray diffraction
KW - Li-O battery
KW - Phenolic antioxidant
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U2 - 10.1016/j.elecom.2017.04.020
DO - 10.1016/j.elecom.2017.04.020
M3 - Article
AN - SCOPUS:85018993130
VL - 79
SP - 68
EP - 72
JO - Electrochemistry Communications
JF - Electrochemistry Communications
SN - 1388-2481
ER -