کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6669835 | 1427286 | 2018 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
NiFe2O4/g-C3N4 heterojunction composite with enhanced visible-light photocatalytic activity
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: NiFe2O4/g-C3N4 heterojunction composite with enhanced visible-light photocatalytic activity NiFe2O4/g-C3N4 heterojunction composite with enhanced visible-light photocatalytic activity](/preview/png/6669835.png)
چکیده انگلیسی
Spinel structure nickel ferrite (NiFe2O4) doped graphitic carbon nitride (g-C3N4) photocatalyst NiFe2O4/g-C3N4 was synthesized by the coprecipitation route to enhance the photocatalytic activity for the visible-light driven degradation of methyl orange. The NiFe2O4 doping content is responsible for the microstructure and photocatalytic activity of NiFe2O4/g-C3N4 samples. Compared with pure NiFe2O4 and g-C3N4, the 2-NiFe2O4/g-C3N4 composite with NiFe2O4 doping of 2.0Â wt% exhibited excellent photocatalytic activity and superior stability after five runs for degrading methyl orange under visible light irradiation. The catalytic activity of 2-NiFe2O4/g-C3N4 sample produced using the coprecipitation route was higher than those of conventional 2-NiFe2O4/g-C3N4 bulks prepared by the impregnation approach. The prepared samples for the photocatalytic degradation of methyl orange followed pseudo-first-order reaction kinetics. It's ascribed to the synergistic effect between NiFe2O4 and g-C3N4, which can inhibit the recombination of photoexcited electron-hole pairs, accelerate photoproduced charges separation, and enhance the visible light absorption.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Saudi Chemical Society - Volume 22, Issue 4, May 2018, Pages 439-448
Journal: Journal of Saudi Chemical Society - Volume 22, Issue 4, May 2018, Pages 439-448
نویسندگان
Yong Liu, Yuchun Song, Yaohui You, Xiaojing Fu, Jing Wen, Xiaogang Zheng,