2011
DOI: 10.1016/j.jpowsour.2011.08.009
|View full text |Cite
|
Sign up to set email alerts
|

Carbon-coated SiO2 nanoparticles as anode material for lithium ion batteries

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

3
183
2
6

Year Published

2014
2014
2022
2022

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 273 publications
(203 citation statements)
references
References 22 publications
3
183
2
6
Order By: Relevance
“…Currently, the best known host material SiO 2 would support high storage capacity as well as alleviate volume change during lithium insertion and extraction, and they attributed this to the effects of Li 2 O or Li 4 SiO 4 [7]. It is known that inert Li 2 O is formed by a reaction of lithium ions with metal oxide.…”
Section: Introductionmentioning
confidence: 99%
“…Currently, the best known host material SiO 2 would support high storage capacity as well as alleviate volume change during lithium insertion and extraction, and they attributed this to the effects of Li 2 O or Li 4 SiO 4 [7]. It is known that inert Li 2 O is formed by a reaction of lithium ions with metal oxide.…”
Section: Introductionmentioning
confidence: 99%
“…This result could be attributed to the stable SiO 2 /C network structure because the amorphous SiO 2 within the composite nanofiber structure reduced to Li 2 O and Li 4 SiO 4 in the initial lithiation process, which could help buffer the volume change caused by the alloying of Si nanoparticles with Li, and thereby increasing the cycling stability by minimizing the pulverization of the active Si material and the loss of electrical contact between Si nanoparticles and the carbon nanofiber matrix. 32,42 From Figure 9, it was also seen that the cycling performance of CVD carbon-coated Si/SiO 2 /C nanofibers was even better than that of Si/SiO 2 /C nanofibers. The capacity retention and coulombic efficiency of CVD carbon-coated Si/SiO 2 /C nanofibers was 91% and 97.4%, respectively, at the 50th cycle.…”
Section: Resultsmentioning
confidence: 97%
“…When SiO 2 was formed in the PVA matrix, the -OH stretching peak of PVA at around 3300 cm −1 was reduced, which could be explained by the intermolecular interaction between the -OH groups of PVA and silica. [30][31][32] In addition, the broad Si-O-Si peak around 1100 cm −1 contained a shoulder at around 1200 cm −1 , which could be attributed to the reaction between -OH groups of PVA and silanol groups of silica. The formation of this new bond and the reduction of -OH bond intensity demonstrated that silica crosslinked with PVA and formed a network structure containing Si-O-PVA-O-Si bridges (Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…[17][18][19][20] Generally, carbonaceous materials are highly attractive for applications in energy conversion and storage systems such as LIB electrode material, 21 the supporting matrix for catalysts in fuel cells, 22 and electrochemical capacitors. 23 Yao et al 24 claimed that C-SiO 2 prepared by pyrolysis product of sucrose coating on SiO 2 particle with 50.1% SiO 2 showed high storage capacity and good cycling stability which remained above 500 mAh g ¹1 at 50th cycle due to the carbon leading to lower interfacial impedance and higher storage capacity. Wang et al 25 prepared nano-sized SiO x /C composite with an O/Si ratio close to 1 exhibited a higher reversible capacity of about 800 mAh g ¹1 but low initial coulombic efficiency, which ensured the good rate capacity by the nano feature of the SiO x /C particle and the electronic conductive nature of carbon coating layer.…”
Section: Introductionmentioning
confidence: 99%