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Synergetic effects of S, N co-doping and surface concave-pores rich in lotus-leaf-like carbon nanosheets enabled threefold lithium storage mechanisms

Authors
Tian, YuLi, MaiZhang, JunxuanLiu, HuiSun, HongranLi, HuifangWang, PengSong, TaeseupPaik, UngyuLiu, Zhiming
Issue Date
Oct-2024
Publisher
Elsevier BV
Keywords
Lithium-ion batteries; Lotus-leaf-like carbon nanosheets; S,N co-doping; Schiff base reaction; Surface-enriched concave pores
Citation
Chemical Engineering Journal, v.497, pp 1 - 10
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Chemical Engineering Journal
Volume
497
Start Page
1
End Page
10
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211764
DOI
10.1016/j.cej.2024.154559
ISSN
1385-8947
1873-3212
Abstract
Carbon-based materials based on structural and dimensional optimization are appealing as anode materials in lithium-ion batteries (LIBs). However rational design of high-efficiency low-dimensional carbon-based electrodes is still challenging. Therefore, a synthesis strategy based on Schiff base reaction has been devised for S, N co-doped and surface-enriched concave pores coupled with two-dimensional lotus-leaf-like carbon nanosheets (S, N-SCP/LCN). Experimental and theoretical results disclose that the synergetic effect of S, N co-doping and surface concave pores synergistically contribute to the improved lithium storage efficiency. The numerous concave pores within the defective carbon substrates significantly enhance the specific surface area and boost the quantity of active sites. Furthermore, S, N co-doping induces additional surface and structural defects and widens the crystallographic spacing. Herein, the formed threefold lithium storage mechanisms work synergistically to increase the active lithium storage sites and ion diffusion channels, promoting ion diffusion and charge transfer during lithium storage. As expected, the S, N-SCP/LCN exhibits remarkably high lithium storage capacity (1250 mAh/g at 0.1 A/g) and exceptional rate performance (445.65 mAh/g at a high rate of 10 A/g).
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