Co2+ substituted for Bi3+ in BiVO4 and its enhanced photocatalytic activity under visible LED light irradiation
المؤلف | Nguyen, Trinh Duy |
المؤلف | Bui, Quynh Thi Phuong |
المؤلف | Le, Tien Bao |
المؤلف | Altahtamouni, T. M. |
المؤلف | Vu, Khanh Bao |
المؤلف | Vo, Dai Viet N. |
المؤلف | Le, Nhan Thi Hong |
المؤلف | Luu, Tuan Duy |
المؤلف | Hong, Seong Soo |
المؤلف | Lim, Kwon Taek |
تاريخ الإتاحة | 2023-08-28T07:16:40Z |
تاريخ النشر | 2019-01-01 |
اسم المنشور | RSC Advances |
المعرّف | http://dx.doi.org/10.1039/c9ra04188e |
الاقتباس | Nguyen, T. D., Bui, Q. T. P., Le, T. B., Altahtamouni, T. M., Vu, K. B., Vo, D. V. N., ... & Lim, K. T. (2019). Co 2+ substituted for Bi 3+ in BiVO 4 and its enhanced photocatalytic activity under visible LED light irradiation. RSC advances, 9(41), 23526-23534. |
الملخص | We investigated the fabrication of Co-doped BiVO4 (Bi1-xCoxVO4+δ, 0.05 < x < 0.5) by the substitution of Co ions for Bi sites in BiVO4. The X-ray diffraction (XRD), Raman, and X-ray photoelectron spectroscopy (XPS) results indicated that the substitution of Co2+ ions for Bi3+ sites in BiVO4 was successful, although a change in the crystal phase of BiVO4 did not occur. UV-vis DRS and PL results suggested that the Co-incorporation could slightly improve the visible light absorption of BiVO4 and induce the separation of photoinduced electron-hole pairs; therefore, a significant enhancement of photocatalytic performance was achieved. The Bi0.8Co0.2VO4+δ sample showed superior photocatalytic activity in comparison with other samples, achieving 96.78% methylene blue (MB) removal within 180 min. In addition, the proposed mechanism of improved photocatalytic activities and the stability of the catalyst were also investigated. |
راعي المشروع | This research is funded by Vietnam National Foundation for Science and Technology Development (NAFOSTED) under grant number 104.05-2017.315. |
اللغة | en |
الناشر | Royal Society of Chemistry |
الموضوع | Aromatic compounds X ray photoelectron spectroscopy |
النوع | Article |
الصفحات | 23526-23534 |
رقم العدد | 41 |
رقم المجلد | 9 |
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