材料科学
多硫化物
氮化物
纳米材料
碳化物
MXenes公司
氮化钒
碳热反应
碳化钒
锡
过渡金属
锂(药物)
硫黄
碳化钛
氧化物
无机化学
氮化硼
化学工程
碳化铌
纳米技术
冶金
图层(电子)
有机化学
化学
物理化学
电极
医学
内分泌学
工程类
电解质
催化作用
作者
Jian Liang Cheong,Chen Hu,Wenwen Liu,Man‐Fai Ng,Michael B. Sullivan,Jackie Y. Ying
出处
期刊:Nano Energy
[Elsevier BV]
日期:2022-08-03
卷期号:102: 107659-107659
被引量:32
标识
DOI:10.1016/j.nanoen.2022.107659
摘要
We report a general and straightforward approach to produce high surface area nanomaterials of transition metal nitride, carbonitride and carbide nanoparticles that are highly dispersed on 3D carbonaceous structure. The preparation of these novel nanomaterials involves a simple one-step heat treatment of a metal precursor and urea-derived graphitic carbon nitride mixture under argon, unlike the conventional methods of using ammonia gas to prepare nitride and high-temperature carbothermal reduction of oxide to produce carbide. With this approach, we have synthesized titanium nitride (TiN/C), vanadium carbonitride (V2CN/C) and niobium carbide-based (NbC/C) nanomaterials using alkoxide precursors. Taking advantage of their high electronic conductivity and surface properties, we have developed the nitrides and carbides as polysulfide (PS) regulators to combat the well-known problems of lithium-sulfur (Li-S) batteries (shuttle phenomena, insulating sulfur, etc.). In particular, V2CN/C nanomaterial was found to possess higher redox activity as compared to TiN/C and NbC/C based on density functional theory (DFT) calculations, polysulfide adsorption studies and various electrochemical experiments. V2CN/C also demonstrated superior performance with an initial specific capacity of 1055 mAh g−1 at 0.2 C and sulfur loading of 4.5 mg cm−2, and a practical areal capacity and capacity retention of ~ 4.2 mAh cm−2 and 89%, respectively, after 300 cycles.
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