TY - JOUR
T1 - Simultaneous remediation of methylene blue and Cr(VI) by mesoporous BiVO4 photocatalyst under visible-light illumination
AU - Xie, Guangyu
AU - Wang, Hui
AU - Zhou, Yaoyu
AU - Du, Yuxuan
AU - Liang, Chong
AU - Long, Linli
AU - Lai, Kaiqi
AU - Li, Wen Xuan
AU - Tan, Xiaofei
AU - Jin, Qi
AU - Qiu, Guoqiang
AU - Zhou, Daixi
AU - Huo, Huiwen
AU - Hu, Xinjiang
AU - Xu, Xiyan
N1 - Publisher Copyright:
© 2020 Taiwan Institute of Chemical Engineers
PY - 2020/7
Y1 - 2020/7
N2 - Porous photocatalysts with large surface areas are more photoactive than compact solid counterparts, owing to their larger surface areas and porous structure, which enhance the adsorption and confinement of light, thus improving the reaction between pollutants and photocatalysts. This paper reports the mechanisms involved in the enhanced photocatalytic activity of two kinds of porous BiVO4 catalysts, named p-BVO-1 and p-BVO-2, which are fabricated by a template-free and alcohol-hydrothermal method, respectively. Characterization, photoelectrochemical and optical measurements, reactive species detection, UV–vis, and XPS analyses were conducted. The results show that the introduction of oxygen vacancies and prolonging effect of light within the pore structure can enhance the photon response and charge separation and transfer, which help to elevate the photocatalytic performance. The simultaneous photocatalysis test of p-BVO-1 for methylene blue (MB) and Cr(VI) showed that the addition of Cr(VI) enhanced MB adsorption by forming an MB-Cr-MB complex, and MB promoted the photoreduction of Cr(VI) by scavenging h+ and ⋅O2−, which may oxidize Cr(III) to Cr(VI). The results indicate that ⋅O2− and h+ are mainly deployed to degrade MB, while e− reduces Cr(VI) ions, thereby favoring the separation of electron-hole pairs.
AB - Porous photocatalysts with large surface areas are more photoactive than compact solid counterparts, owing to their larger surface areas and porous structure, which enhance the adsorption and confinement of light, thus improving the reaction between pollutants and photocatalysts. This paper reports the mechanisms involved in the enhanced photocatalytic activity of two kinds of porous BiVO4 catalysts, named p-BVO-1 and p-BVO-2, which are fabricated by a template-free and alcohol-hydrothermal method, respectively. Characterization, photoelectrochemical and optical measurements, reactive species detection, UV–vis, and XPS analyses were conducted. The results show that the introduction of oxygen vacancies and prolonging effect of light within the pore structure can enhance the photon response and charge separation and transfer, which help to elevate the photocatalytic performance. The simultaneous photocatalysis test of p-BVO-1 for methylene blue (MB) and Cr(VI) showed that the addition of Cr(VI) enhanced MB adsorption by forming an MB-Cr-MB complex, and MB promoted the photoreduction of Cr(VI) by scavenging h+ and ⋅O2−, which may oxidize Cr(III) to Cr(VI). The results indicate that ⋅O2− and h+ are mainly deployed to degrade MB, while e− reduces Cr(VI) ions, thereby favoring the separation of electron-hole pairs.
KW - BiVO
KW - Cr(Ⅵ)
KW - Methylene blue
KW - Photocatalysis
KW - Porous semiconductor
UR - http://www.scopus.com/inward/record.url?scp=85087504433&partnerID=8YFLogxK
U2 - 10.1016/j.jtice.2020.05.014
DO - 10.1016/j.jtice.2020.05.014
M3 - Article
AN - SCOPUS:85087504433
SN - 1876-1070
VL - 112
SP - 357
EP - 365
JO - Journal of the Taiwan Institute of Chemical Engineers
JF - Journal of the Taiwan Institute of Chemical Engineers
ER -