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以2,4,6-三苯基硼酸为成膜电解质添加剂在高压LiNiCoMnO阴极上构建低阻抗界面用于锂离子电池

Constructing a Low-Impedance Interface on a High-Voltage LiNiCoMnO Cathode with 2,4,6-Triphenyl Boroxine as a Film-Forming Electrolyte Additive for Li-Ion Batteries.

作者信息

Li Guanjie, Liao Youhao, Li Zifei, Xu Ning, Lu Yikeng, Lan Guangyuan, Sun Gengzhi, Li Weishan

机构信息

School of Chemistry, South China Normal University, Guangzhou 510006, China.

National and Local Joint Engineering Research Center of MPTES in High Energy and Safety LIBs, Engineering Research Center of MTEES (Ministry of Education), and Key Laboratory of ETESPG (GHEI), South China Normal University, Guangzhou 510006, China.

出版信息

ACS Appl Mater Interfaces. 2020 Aug 19;12(33):37013-37026. doi: 10.1021/acsami.0c05623. Epub 2020 Aug 10.

Abstract

Compared with other commercial cathode materials, the LiNiCoMnO cathode (NCM811) has high specific capacity and a relatively low cost. Nevertheless, the higher nickel content in NCM811 leads to an extremely unstable interface between the electrode and the electrolyte, resulting in inferior cyclic stability of the corresponding cell. Use of film-forming additives is regarded as the most feasible and economic approach to construct a stable interface on the NCM811 cathode. However, less effective electrolyte additives have been reported to date. Herein, we propose a valid film-forming electrolyte additive, 2,4,6-triphenyl boroxine (TPBX), for application in a high-voltage NCM811 cathode. Experimental and computational results reveal that the TPBX additive can be preferentially oxidized to generate a highly stable and conductive cathode electrolyte interface (CEI) layer on the NCM811 cathode, which efficiently suppresses the detrimental side reaction and improves the electrochemical performance eventually. In detail, the cyclic stability of the Li/NCM811 half-cell is enhanced from 57% (without additive) to 78% (with 5% TPBX) after 200 cycles at 1 between 3.0 and 4.35 V. At a high current rate of 15, the TPBX-containing electrode delivers a capacity of about 135 mAh g, which is much higher than that of the electrode without the additive (80 mAh g). Interestingly, the TPBX is also reduced earlier than the ethylene carbonate (EC) solvent to form an ionically conductive solid electrolyte interface (SEI) film on the graphite anode. Due to the CEI layer on the cathode and the SEI film on the anode simultaneously formed by the TPBX additive, the cyclic performance of the graphite/LiNiCoMnO full cell is enhanced. Therefore, the incorporation of the TPBX additive into the electrolyte provides a convenient method for the commercial application of the high-energy-density NCM811 cathode in high-voltage lithium-ion batteries.

摘要

与其他商用正极材料相比,锂镍钴锰氧化物正极(NCM811)具有高比容量和相对较低的成本。然而,NCM811中较高的镍含量导致电极与电解质之间的界面极不稳定,从而使相应电池的循环稳定性较差。使用成膜添加剂被认为是在NCM811正极上构建稳定界面最可行且经济的方法。然而,迄今为止报道的电解质添加剂效果欠佳。在此,我们提出一种有效的成膜电解质添加剂2,4,6-三苯基硼酸酯(TPBX),用于高压NCM811正极。实验和计算结果表明,TPBX添加剂可优先被氧化,在NCM811正极上生成高度稳定且导电的正极电解质界面(CEI)层,有效抑制有害的副反应并最终改善电化学性能。具体而言,Li/NCM811半电池在3.0至4.35 V之间以1C循环200次后,其循环稳定性从57%(无添加剂)提高到78%(含5% TPBX)。在15C的高电流速率下,含TPBX的电极提供约135 mAh/g的容量,远高于不含添加剂的电极(80 mAh/g)。有趣的是,TPBX也比碳酸亚乙酯(EC)溶剂更早被还原,在石墨阳极上形成离子导电的固体电解质界面(SEI)膜。由于TPBX添加剂同时在阴极形成CEI层和在阳极形成SEI膜,石墨/LiNiCoMnO全电池的循环性能得到增强。因此,将TPBX添加剂引入电解质为高能量密度NCM811正极在高压锂离子电池中的商业应用提供了一种便捷方法。

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