紫外线
氮气
紫外线辐射
材料科学
辐射
光热治疗
化学
光电子学
分析化学(期刊)
纳米技术
物理
光学
放射化学
环境化学
有机化学
作者
Yongfang Liang,Man Cai,Jianghai Li,Lin Li,Hongying Zhao,Jinyu Wu,Xianqing Liang,Wenzheng Zhou,Haifu Huang
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-05-01
被引量:1
标识
DOI:10.1021/acs.langmuir.5c01015
摘要
Two-dimensional MXenes have emerged as exceptional electrode materials for supercapacitors (SCs), making them highly attractive for energy storage and conversion applications. However, their electrochemical performance is strongly influenced by surface terminal groups and interlayer spacing. In this study, we introduce an ultraviolet(UV)-induced nitrogen-doping method that employs UV radiation to promote the thermal decomposition of ammonium oxalate while inducing nitrogen-doping. The resulting UV-induced nitrogen-doped Ti3C2Tx (I-Ti3C2Tx-N) exhibits a high N doping level of 1.46 at. % and an expanded lattice spacing of 1.43 nm. As a result, I-Ti3C2Tx-N demonstrates exceptional pseudocapacitance performance, achieving a remarkable specific capacitance of 466.28 F g-1, significantly exceeding that of raw Ti3C2Tx (367.96 F g-1). Furthermore, when integrated into a quasi-solid-state SC device, it delivers an impressive energy density of 12.58 Wh kg-1 at a power density of 250.00 W kg-1. The enhanced electrochemical performance of I-Ti3C2Tx-N is attributed to the effects of UV radiation, which introduces N terminal groups, eliminates detrimental -F and -OH terminals, and increases interlayer spacing. This study highlights a simple yet effective UV-induced nitrogen-doping method for modifying MXene materials, offering another way for optimizing their electrochemical properties in energy storage applications.
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