UV-Assisted Cataluminescent Sensor for Carbon Monoxide Based on Oxygen-Functionalized g-C3N4 Nanomaterials

被引:37
|
作者
Li, Li [1 ]
Deng, Dongyan [1 ]
Huang, Shixu [1 ]
Song, Hongjie [1 ]
Xu, Kailai [1 ]
Zhang, Lichun [1 ]
Lv, Yi [1 ,2 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Sichuan, Peoples R China
[2] Sichuan Univ, Analyt & Testing Ctr, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-FREE CATALYST; VOLATILE ORGANIC-COMPOUNDS; GAS SENSOR; UTILIZING CHEMILUMINESCENCE; SELECTIVE OXIDATION; SUPPORTED GOLD; NITRIDE; CO; PERFORMANCE; MECHANISM;
D O I
10.1021/acs.analchem.8b02532
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cataluminescence (CTL) is one of the most important sensing-transduction principles for the real-time monitoring of atmospheric pollutants. Highly sensitive CTL-based CO detection still remains a challenge because of the relatively poor reactivity of CO and the low catalytic efficiency of the catalysts. Herein, combining ultraviolet (UV)-light activation and chemical modification of the sensing element, we have successfully established a UV-assisted CTL sensor for gaseous CO based on g-C3N4 with high sensitivity, selectivity, and stability. UV irradiation can efficiently activate CO molecules and induce the generation of reactive oxygen species (ROS) for CO oxidation. Furthermore, carboxyl groups greatly facilitate the chemisorption of CO on functionalized g-C3N4 nanomaterials, thus enhancing the CTL sensitivity. The influences of experimental conditions and the possible catalytic mechanism of CO on functionalized g-C3N4 have been investigated in detail. Under the optimal experimental conditions, the proposed CTL sensor presents a detection limit (3 sigma) toward CO of 0.008 mu g mL(-1), which is much lower than the maximum allowable emission concentration of CO in atmospheric conditions (0.030 mu g mL(-1)). The UV-CTL system is green, sensitive, stable, and low cost, and thus it possesses great potential application in gas sensing.
引用
收藏
页码:9598 / 9605
页数:8
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