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Li Pre-Doping of Amorphous Si Thin Flakes in Li-Aromatic Complex Solutions
Another serious problem for Si negative-electrode is a large irreversible capacity (Qirr) in the first cycle. Li pre-doping is a useful technique to cancel the large Qirr. We also reported that the large Qirr (1000~1500 mAh g−1) can be drastically reduced by Li pre-doping using a direct contact method with Li foil.2) Unfortunately, however, several issues, such as control of Li-doping level and homogenous Li-doping, remained to be solved for practical use.
In this study, we developed a Li pre-doping technique for the amorphous Si-LP electrode using Li-naphthalene and Li-anthracene complex solutions.3)
The Si-LP composite electrode consisted of 83.3 wt.% Si-LP, 5.6 wt.% Ketjen black, and 11.1 wt.% carboxymethyl cellulose sodium salt. The Si-LP electrode was pre-doped using a coin-type two-electrode cell and Li foil as a lithium source and a reference electrode. The solutions were tetrahydrofuran (THF) containing naphthalene (NTL) or anthracene (ATC) of which the concentration ranged from 0.1 to 1.0 M. The pre-doping was carried out by leaving the cell for a given time under the open-circuit condition. The variation of open circuit voltage (OCV) with time was monitored. After pre-doping, the cell was disassembled in an Ar-filled glove box and then the Si-LP electrode was rinsed with pure THF to remove the residual solution.
Charge and discharge properties of the pre-doped Si-LP electrodes were investigated using a coin-type two-electrode half-cell at a C/6 rate (1 C = 4200 mAh g-1) at 30oC. The working and counter electrodes were the pre-doped Si-LP electrode and a Li foil, respectively. The electrolyte used was 1.0 M LiPF6/EC+DEC (1:1 by vol.).
Figure 1 shows the variation of OCV of pre-doping cells with time. The voltages descended to about 60 and 40 mV within 5 h after the start of pre-doping in 0.1 and 0.5 M Li-NTL solution, respectively. On the other hands, the voltage almost unchanged at around 240 mV during the first 10 h for Li-ATC, and then began to decrease gradually.
Table 1 shows charge capacity (Qcha), discharge capacity (Qdis) and pre-doped capacity (Qpre) of the Si-LP electrodes in the 1st cycle in 1.0 M LiPF6 / EC + DEC after pre-doping in Li-NTL or -ATC complex solution. If the irreversible capacity is about 1200 mAh g-1, which corresponds to the initial irreversible capacity of pristine Si-LP electrodes in 1.0 M LiPF6/EC+DEC, Qpreis calculated from the following equation;
Qpre = Qdis – Qcha + 1200 mAh g-1
As a result, Qpre was 2345 and 2429 mAh g-1 for 1 h pre-doping in 0.5 M Li-NTL and 10 h pre-doping in 0.1 M Li-NTL solution, respectively. These values were close to typical reversible capacity of Si-LP (about 2300 mAh g-1). These results suggest that the Si-LP electrodes were fully pre-doped in these conditions.
On the other hands, the Qdis was almost the same as Qcha, for 1 h pre-doping in 0.1 M Li-NTL solution, that is, the Qpre compensated for Qirr. The OCV at the end of pre-doping was 110 mV, as shown in Fig. 1. Very similar results were obtained for 22 h pre-doping in Li-ATC solution; Qdis was close to Qcha and the OCV reached 140 mV at the end of pre-doping. To clarify the meaning of the OCV, a pristine Si-LP electrode was charged at a constant voltage of 120 mV for 3 h, and then discharged. The discharge capacity was evaluated to be 1500 mAh g-1, which was almost equivalent to Qirr of 1200 mAh g-1. These results indicate that Li-doping level can be controlled by OCV.
References
1) M. Saito et al., Solid State Ionics, 225, 506 (2012).
2) T. Okubo et al., Solid State Ionics, 262, 39 (2014).