TY - JOUR
T1 - Graphitic carbon nitride embedded with graphene materials towards photocatalysis of bisphenol A
T2 - The role of graphene and mediation of superoxide and singlet oxygen
AU - Chen, Yu Hsin
AU - Wang, Bo Kai
AU - Hou, Wen Che
N1 - Funding Information:
Financial support provided by the Ministry of Science and Technology (MOST) of Taiwan (for Hou) under grant number MOST 107-2628-E-006-001-MY3 is acknowledged.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/9
Y1 - 2021/9
N2 - Composite photocatalysts comprising graphitic carbon nitride (g-C3N4) and graphene materials were synthesized and evaluated in the photocatalysis of bisphenol A (BPA) with a focus on elucidating the reaction mechanism. Embedding reduced graphene oxide (rGO) to g-C3N4 significantly accelerated the photocatalysis rate of BPA by three folds under visible light irradiation at neutral pH. We showed that rGO synthesized in intimate contact with g-C3N4 increased the surface areas and electrical conductivity of the g-C3N4 composites and promoted the electron-hole pair separation. The BPA photodegradation mechanism involved selective oxidants as superoxide (O2•−) and singlet oxygen (1O2) that were formed through one-electron reduction of O2 and the unique oxidation of O2•− by photogenerated hole (h+), respectively. The synthesized photocatalyst exhibited superior visible light photoreactivity to that of N-doped P25 TiO2, good photo-stability and reuse potential, and was operative in complex wastewater. rGO embedded g-C3N4 achieved good photomineralization of BPA at 80% in 4 h compared to 40% of bare g-C3N4. This study sheds light on the photocatalysis mechanism of BPA with a metal-free, promising rGO/g-C3N4 photocatalyst.
AB - Composite photocatalysts comprising graphitic carbon nitride (g-C3N4) and graphene materials were synthesized and evaluated in the photocatalysis of bisphenol A (BPA) with a focus on elucidating the reaction mechanism. Embedding reduced graphene oxide (rGO) to g-C3N4 significantly accelerated the photocatalysis rate of BPA by three folds under visible light irradiation at neutral pH. We showed that rGO synthesized in intimate contact with g-C3N4 increased the surface areas and electrical conductivity of the g-C3N4 composites and promoted the electron-hole pair separation. The BPA photodegradation mechanism involved selective oxidants as superoxide (O2•−) and singlet oxygen (1O2) that were formed through one-electron reduction of O2 and the unique oxidation of O2•− by photogenerated hole (h+), respectively. The synthesized photocatalyst exhibited superior visible light photoreactivity to that of N-doped P25 TiO2, good photo-stability and reuse potential, and was operative in complex wastewater. rGO embedded g-C3N4 achieved good photomineralization of BPA at 80% in 4 h compared to 40% of bare g-C3N4. This study sheds light on the photocatalysis mechanism of BPA with a metal-free, promising rGO/g-C3N4 photocatalyst.
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U2 - 10.1016/j.chemosphere.2021.130334
DO - 10.1016/j.chemosphere.2021.130334
M3 - Article
C2 - 34126674
AN - SCOPUS:85103986750
SN - 0045-6535
VL - 278
JO - Chemosphere
JF - Chemosphere
M1 - 130334
ER -