A Commercial Conducting Polymer as Both Binder and Conductive Additive for Silicon Nanoparticle-Based Lithium-Ion Battery Negative Electrodes

作者：Higgins, Thomas M.; Park, Sang-Hoon; King, Paul J.; Zhang, Chuanfan; MoEvoy, Niall; Berner, Nina C.; Daly, Dermot; Shmeliov, Aleksey; Khan, Umar; Due**erg, Georg; Nicolosi, Valeria^*; Coleman, Jonathan N.^*

来源：ACS Nano, 2016, 10(3): 3702-3713.

DOI：10.1021/acsnano.6b00218

• anode
• battery
• binder
• conducting polymer
• conducting additive
• negative electrode
• PEDOT:PSS
• silicon

This work describes silicon nanoparticlebased lithium -ion battery negative electrodes where multiple nonactive electrode additives (usually carbon black and an inert polymer binder) are replaced with a single conductive binder, in this case, the conducting polymer PEDOT:PSS. While enabling the production of well -mixed slurry -cast electrodes with high silicon content (up to 95 wt %), this combination eliminates the well-known occurrence of capacity losses due to physical separation of the silicon and traditional inorganic conductive additives during repeated lithiation/delithiation processes. Using an in situ secondary doping treatment of the PEDOT:PSS with small quantities of formic acid, electrodes containing 80 wt % SiNPs can be prepared with electrical conductivity as high as 4.2 S/cm. Even at the relatively high areal loading of 1 mg/cm(2), this system demonstrated a first cycle lithiation capacity of 3685 inkh/g (based on the SiNP mass) and a first, cycle efficiency of 78%. After 100 repeated cycles at 1 A/g this electrode was still able to store an impressive 1950 mAth/g normalized to Si mass (-75% capacity retention), corresponding to 1542 mAh/g when the capacity is normalized by the total electrode mass. At the maximum electrode thickness studied (-4.5 mg/cm2), a high areal capacity of 3 mA.h/cm(2) was achieved. Importantly, these electrodes are based on commercially available components and are produced by the standard slurry coating methods required for large-scale electrode production. Hence, the results presented here are highly relevant for the realization of commercial LiB negative electrodes that surpass the performance of current graphite-based negative electrode systems.

• 出版日期2016-3