TY - JOUR
T1 - Surface functional group-tailored B and N co-doped carbon quantum dot anode for lithium-ion batteries
AU - Kim, Kue Ho
AU - Ahn, Hyo Jin
N1 - Publisher Copyright:
© 2022 John Wiley & Sons Ltd.
PY - 2022/5
Y1 - 2022/5
N2 - Recently, carbon quantum dots (CQDs) have emerged as new surface modification agents for the anode materials of lithium-ion batteries (LIBs) owing to their various advantages, including high surface area, low toxicity, low cost, and chemical stability. However, CQDs intrinsically possess large amounts of nonessential oxygen-containing groups (C-O and C-OH) at the surface, which can inhibit Li+ accessibility and lower electrical conductivity. Owing to these limitations, CQDs have been widely studied as composite agents and not as independent active materials. Therefore, to enhance the electrical conductivity and increase the Li+ diffusivity of CQDs, we suggest surface functional group-tailored boron and nitrogen co-doped carbon quantum dots (BN-CQDs) for self-reliant LIB anode applications. The 0.5BN-CQD electrodes showed superior electrochemical performance, including outstanding ultrafast energy storage capability (130.4 mAh g−1 at 3000 mA g−1 with capacity retention of 88% up to 1000 cycles). This is contributed by the enhanced electrical conductivity of the boron and nitrogen co-doped structure and high Li+ acceptability, which facilitated the formation of C═O surface functional groups due to the boron dopant. In this regard, we believe that the fabrication of self-reliant 0.5BN-CQD electrodes could be a promising research strategy for carbon-based anode materials.
AB - Recently, carbon quantum dots (CQDs) have emerged as new surface modification agents for the anode materials of lithium-ion batteries (LIBs) owing to their various advantages, including high surface area, low toxicity, low cost, and chemical stability. However, CQDs intrinsically possess large amounts of nonessential oxygen-containing groups (C-O and C-OH) at the surface, which can inhibit Li+ accessibility and lower electrical conductivity. Owing to these limitations, CQDs have been widely studied as composite agents and not as independent active materials. Therefore, to enhance the electrical conductivity and increase the Li+ diffusivity of CQDs, we suggest surface functional group-tailored boron and nitrogen co-doped carbon quantum dots (BN-CQDs) for self-reliant LIB anode applications. The 0.5BN-CQD electrodes showed superior electrochemical performance, including outstanding ultrafast energy storage capability (130.4 mAh g−1 at 3000 mA g−1 with capacity retention of 88% up to 1000 cycles). This is contributed by the enhanced electrical conductivity of the boron and nitrogen co-doped structure and high Li+ acceptability, which facilitated the formation of C═O surface functional groups due to the boron dopant. In this regard, we believe that the fabrication of self-reliant 0.5BN-CQD electrodes could be a promising research strategy for carbon-based anode materials.
KW - Li-ion battery
KW - anode
KW - carbon quantum dot
KW - co-doped structure
KW - ultrafast energy storage
UR - http://www.scopus.com/inward/record.url?scp=85124607592&partnerID=8YFLogxK
U2 - 10.1002/er.7738
DO - 10.1002/er.7738
M3 - Article
AN - SCOPUS:85124607592
SN - 0363-907X
VL - 46
SP - 8367
EP - 8375
JO - International Journal of Energy Research
JF - International Journal of Energy Research
IS - 6
ER -