In situ fabrication of dual coating structured SiO/1D-C/a-C composite as high-performance lithium ion battery anode by fluidized bed chemical vapor deposition

To notably improve the cycling stability of high-capacity SiO anode, an ingenious carbon dual coating structure was proposed, utilizing the high conductivity of 1D carbon (1D-C) and the excellent buffering of amorphous carbon (a-C). The carbon deposition pattern by regulating process temperatures wa...

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Veröffentlicht in:Carbon (New York) 2020-10, Vol.168, p.113-124
Hauptverfasser: Shi, Hebang, Zhang, He, Li, Xinxin, Du, Yu, Hou, Guolin, Xiang, Maoqiao, Lv, Pengpeng, Zhu, Qingshan
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container_end_page 124
container_issue
container_start_page 113
container_title Carbon (New York)
container_volume 168
creator Shi, Hebang
Zhang, He
Li, Xinxin
Du, Yu
Hou, Guolin
Xiang, Maoqiao
Lv, Pengpeng
Zhu, Qingshan
description To notably improve the cycling stability of high-capacity SiO anode, an ingenious carbon dual coating structure was proposed, utilizing the high conductivity of 1D carbon (1D-C) and the excellent buffering of amorphous carbon (a-C). The carbon deposition pattern by regulating process temperatures was explored. An evolutive carbon deposition mechanism between 1D-C and a-C was deduced, which was a competitive mode between low-temperature catalytic growth and high-temperature pyrolysis deposition. Motivated by the deduced carbon deposition mechanism, a novel two-step coating process via fluidized bed chemical vapor deposition was proposed to fabricate the SiO/1D-C/a-C composite. The grown thickened 1D-C and deposited a-C were heterogeneously coated on the SiO particle surface, forming an ingenious dual coating structure. The synthesized SiO/1D-C/a-C exhibited extremely significant enhanced cycling stability, which showed a reversible capacity of 1012 mAh g−1 (capacity retention of 88.3%) after 120 cycles. The thickened 1D-C is entangled with each other to form a three-dimensional conductive network, while the deposited a-C formed a shell-like coating to buffer the volume expansion during cycling. The unique carbon dual coating structure achieved synergistic strengthening, which guarantees the superior electrochemical performance of the SiO/1D-C/a-C. [Display omitted]
doi_str_mv 10.1016/j.carbon.2020.06.053
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The carbon deposition pattern by regulating process temperatures was explored. An evolutive carbon deposition mechanism between 1D-C and a-C was deduced, which was a competitive mode between low-temperature catalytic growth and high-temperature pyrolysis deposition. Motivated by the deduced carbon deposition mechanism, a novel two-step coating process via fluidized bed chemical vapor deposition was proposed to fabricate the SiO/1D-C/a-C composite. The grown thickened 1D-C and deposited a-C were heterogeneously coated on the SiO particle surface, forming an ingenious dual coating structure. The synthesized SiO/1D-C/a-C exhibited extremely significant enhanced cycling stability, which showed a reversible capacity of 1012 mAh g−1 (capacity retention of 88.3%) after 120 cycles. The thickened 1D-C is entangled with each other to form a three-dimensional conductive network, while the deposited a-C formed a shell-like coating to buffer the volume expansion during cycling. The unique carbon dual coating structure achieved synergistic strengthening, which guarantees the superior electrochemical performance of the SiO/1D-C/a-C. 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The unique carbon dual coating structure achieved synergistic strengthening, which guarantees the superior electrochemical performance of the SiO/1D-C/a-C. 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subjects Anodes
Batteries
Buffers
Carbon
Chemical vapor deposition
Coating
Cycles
Electrochemical analysis
Fluidized beds
High temperature
Lithium
Lithium-ion batteries
Low temperature
Pyrolysis
Rechargeable batteries
title In situ fabrication of dual coating structured SiO/1D-C/a-C composite as high-performance lithium ion battery anode by fluidized bed chemical vapor deposition
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