کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7993911 | 1516155 | 2018 | 42 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
A facile one-step hydrothermal synthesis of NiO/ZnO heterojunction microflowers for the enhanced formaldehyde sensing properties
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
فلزات و آلیاژها
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
NiO/ZnO heterojunction microflowers were successfully synthesized by using a facile one-step hydrothermal process followed by calcination. The structural features were mainly characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). It is found that the obtained products showed flower-like structures assembled by a number of ZnO porous nanosheets, and which were successfully retained after introducing NiO. The formaldehyde gas sensing properties were systematically investigated between the pure and NiO/ZnO microflowers. NiO/ZnO microflower sensor exhibited the enhanced response and lower operating temperature compared to pure one. Especially, the 3â¯mol% NiO/ZnO microflower sensor exhibited the highest responses compared with others at a relatively lower operating temperature of 200â¯Â°C. In addition, fast response and recovery, good reproducibility and stability, and good selectivity to formaldehyde were also obtained, indicating the formation of NiO/ZnO heterojunction in favor of improving the sensing properties. Meanwhile, the sensing enhancement mechanism of the NiO/ZnO microflowers was also discussed, which is related to the formation of hetrojunction at interface and the high catalytic activity of NiO.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Alloys and Compounds - Volume 739, 30 March 2018, Pages 260-269
Journal: Journal of Alloys and Compounds - Volume 739, 30 March 2018, Pages 260-269
نویسندگان
Xiaoguang San, Ming Li, Dongyu Liu, Guosheng Wang, Yanbai Shen, Dan Meng, Fanli Meng,