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
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