共 50 条
Graphdiyne and its heteroatom-doped derivatives for Li-ion/metal batteries
被引:0
|作者:
Shang, Hong
[1
]
Peng, Jia
[1
]
Zhou, Yougui
[1
]
Guo, Lihua
[1
]
Li, Huipeng
[1
]
Wang, Weiliang
[2
]
机构:
[1] China Univ Geosci Beijing, Sch Sci, Beijing 100083, Peoples R China
[2] China Univ Geosci Beijing, Sch Energy Resources, Beijing 100083, Peoples R China
基金:
中国国家自然科学基金;
关键词:
METAL-FREE ELECTROCATALYST;
ENERGY-STORAGE;
CARBON;
REDUCTION;
GRAPHYNES;
GRAPHENE;
PREDICTIONS;
NANOSHEETS;
NANOWALLS;
ANODE;
D O I:
10.1039/d4dt03268c
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Graphdiyne (GDY), which is composed of benzene rings and acetylene linkage units, is a new allotrope of carbon material. In particular, the large triangular pores of GDY, with a diameter of 5.4 & Aring;, theoretically predict a higher lithium embedding density than traditional graphite anodes, making it a promising candidate for energy storage materials in lithium-ion (Li-ion) batteries. GDY is primarily synthesized via a cross-coupling reaction of hexaethynylbenzene (HEB). Under similar preparation conditions, the cross-coupling reaction of aryne precursors, other than HEB, yields many GDY heteroatom-doped derivatives. This introduces numerous heteroatomic defects as well as electrochemically active sites, potentially enhancing electrochemical performance. Recent advancements have focused on utilizing GDY and its heteroatom-doped derivatives as electrode materials or composite materials in Li-ion/metal batteries. This review systematically summarizes the strategies developed for GDY and its heteroatom-doped derivatives. Notably, recent research on the effects of morphology and chemical/electronic structure on performance, particularly new conceptual mechanisms in Li-ion/metal batteries, including self-expanding Li-ion transport channels and a capture/pore filling-intercalation hybrid mechanism, is briefly described. The results presented herein highlight the significant potential of GDY and its heteroatom-doped derivatives for energy storage applications and inspire further development.
引用
收藏
页码:3551 / 3572
页数:22
相关论文