Microjunction-Modulated Selective Ammonia Sensor with P-Type Oxides-Decorated WS2 Microflakes

材料科学 非阻塞I/O 三甲胺 选择性 异质结 漫反射红外傅里叶变换 吸附 傅里叶变换红外光谱 光电子学 化学工程 物理化学 有机化学 光催化 催化作用 化学 工程类
作者
Qiyilan Guang,Shupeng Sun,Baoyu Huang,Jianwei Zhang,Nan Wang,Xiaogan Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (6): 7565-7575 被引量:3
标识
DOI:10.1021/acsami.3c16519
摘要

In this study, p-type oxides including NiO, Co3O4, and CuO had been heterostructured with WS2 microflakes for chemiresistive-type gas sensors at room temperature. Microjunctions formed between p-type oxides and WS2 microflakes effectively modulated the sensitivities of the sensors to ammonia. In comparison to Co3O4- or CuO-decorated WS2-based sensors in which "deep energy puddles" were formed at the microjunctions between the oxides and WS2, the fabricated NiO/WS2 heterostructure-based sensor without the formed energy puddles exhibited a better sensing performance with improved sensitivity and a faster response to gaseous 1–10 ppm of NH3. It also processes a good selectivity to some volatile organic compounds including HCHO, toluene, CH3OH, C2H5OH, CH3COCH3, and trimethylamine (TMA). The underlying mechanisms for the enhanced responses were examined by employing in situ diffuse reflectance infrared Fourier transform spectroscopy and density functional theory computation. The oxidization of NH3 on NiO/WS2 was much more intensified compared to those occurred on Co3O4/WS2 and CuO/WS2. NiO/WS2 has a stronger adsorption to NH3 and gains more effective charges transferred from NH3 which significantly contributes to the enhanced sensing properties.
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