Tris(hexafluoro-iso-propyl)phosphate as an SEI-Forming Additive on Improving the Electrochemical Performance of the Li[Li0.2Mn0.56Ni0.16Co0.08]O2 Cathode Material

Highly fluorinated phosphate ester, tri(hexafluoro-iso-propyl)phosphate ((C3HF6O)3PO or HFiP), has been investigated as an additive to improve the cycling performance of lithium-rich cathode material Li[Li0.2Mn0.56Ni0.16Co0.08]O2. The capacity retention for the Li[Li0.2Mn0.56Ni0.16Co0.08]O2 electrod...

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Veröffentlicht in:Journal of the Electrochemical Society 2013, Vol.160 (2), p.A285-A292
Hauptverfasser: Tan, Shi, Zhang, Zhongru, Li, Yixiao, Li, Yun, Zheng, Jianming, Zhou, Zhibin, Yang, Yong
Format: Artikel
Sprache:eng
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Zusammenfassung:Highly fluorinated phosphate ester, tri(hexafluoro-iso-propyl)phosphate ((C3HF6O)3PO or HFiP), has been investigated as an additive to improve the cycling performance of lithium-rich cathode material Li[Li0.2Mn0.56Ni0.16Co0.08]O2. The capacity retention for the Li[Li0.2Mn0.56Ni0.16Co0.08]O2 electrode in 1% HFiP-added electrolyte after 130 cycles is 73.3%, which is higher than that for the reference electrolyte (64.5%). The capacity-retention mechanism is investigated via a combination of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscope (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). CV results show that HFiP additive decomposes on the surface of cathode material at a relatively lower voltage (∼4.2 V) than that of solvents in the reference electrolyte. EIS, SEM, TEM along with XPS measurements indicate that a more stable SEI layer is formed on the cathode surface with the presence of decomposition products of HFiP additive. Thus, electrodes cycled in HFiP-added electrolyte have much more stable solid electrolyte interface impedance and relatively smaller charge transfer resistance than that cycled in additive free electrolyte. The stabilization of the electrode/electrolyte interface is beneficial to enhance the electrochemical performance of Li[Li0.2Mn0.56Ni0.16Co0.08]O2.
ISSN:0013-4651
DOI:10.1149/2.066302jes