Fabrication of Ag-Deposited Silicon Nanoparticles for a Lithium Ion Battery Anode Prepared By Alkaline Immersion Plating

Tuesday, October 13, 2015
West Hall 1 (Phoenix Convention Center)
Y. Sugawara (Shinshu University) and S. Arai (Shinshu University)

Lithium ion batteries (LIBs) with greater       energy density are required for use in energy-demanding applications such as electric cars and electronic devices. Silicon is an attractive candidate anode material for use in LIBs due to its high theoretical capacity (4200 mAh/g) compared to carbon (372 mAh/g) currently used in commercially available lithium ion batteries.

The commercial use of Si-based powders in anodes remains hindered by the low electrical conductivity of silicon and its huge volume change during lithiation and delithiation.

Many studies have been conducted to alleviate the pulverization of silicon during the charge/discharge process and to increase the conductivity of silicon materials. Recently, several approaches for synthesizing 3D porous Si-based anode materials that exhibit good cycling characteristics have been developed. Several approaches employ a wet-chemical etching process using hydrofluoric acid (HF) and silver nitrate (AgNO3). The fabrication process consists of two steps. First, Ag is deposited on silicon nanoparticles using HF and AgNO3. Subsequently, the particles are immersed into HF and hydrogen peroxide (H2O2), resulting in the generation of 3D porous silicon nanoparticles. However, HF is a dangerous chemical and thus a process not requiring HF for the fabrication of Ag-deposited silicon particles is required.1,2,3)

Herein, we present Ag-deposited silicon nanoparticles

fabricated using an alkaline method and describe their charge/discharge properties as a LIB anode material.


We used planetary ball milling silicon nanoparticles. An immersion plating bath containing 2 g/L Si, 0.005 M AgNO3 and 0.010 M EDTA-2Na was prepared, and KOH was then added to adjust to pH 9~12. The silicon nanoparticles were dispersed using ultrasonic irradiation for 30 min. The reaction was conducted in a water bath to maintain the temperature at 25, 30 40, 50, 60, 70, 80°C, respectively for 2 hours. The silicon nanoparticles were then collected on a filter by suction filtration and dried in vacuum at 110 °C for 2 hours.

The microstructures of the samples were observed using field-emission scanning electron microscopy (FE-SEM) and scanning-transmission electron microscopy (STEM). Charge-discharge cycle tests of the prepared samples were performed. A coin cell (Model CR2032) was used as the test cell and lithium metal foil was used as the counter electrode. The cut-off potentials for the charge/discharge processes were 0.02 V and 1.5 V (vs. Li/Li+).


Ag-deposited silicon nanoparticles were fabricated using an alkaline immersion plating method in the absence of HF.


1)       Jung-In Lee, Soojin Park Nano Energy (2013) 2, 146-152

2)       Satoshi Uchida, Megumi Mihashi, Masaki Yamagata, Masashi Ishikawa, Journal of Power Sources 273 (2015) 118-122

3)       Chunli Li, Ping Zhang, Zhiyu Jiang Electrochemica Acta 161 (2015) 408-412