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

材料科学 电极 锂(药物) 化学工程 纳米颗粒 电池(电) 导电体 锂离子电池 泥浆 纳米技术 复合材料 光电子学 化学 医学 功率(物理) 物理 物理化学 量子力学 工程类 内分泌学
作者
Thomas M. Higgins,Sang‐Hoon Park,Paul J. King,Chuanfang Zhang,Niall McEvoy,Nina C. Berner,Dermot Daly,Aleksey Shmeliov,Umar Khan,Georg S. Duesberg,Valeria Nicolosi,Jonathan N. Coleman
出处
期刊:ACS Nano [American Chemical Society]
卷期号:10 (3): 3702-3713 被引量:481
标识
DOI:10.1021/acsnano.6b00218
摘要

This work describes silicon nanoparticle-based 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 mA·h/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 mA·h/g normalized to Si mass (∼75% capacity retention), corresponding to 1542 mA·h/g when the capacity is normalized by the total electrode mass. At the maximum electrode thickness studied (∼1.5 mg/cm(2)), 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.
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