TY - JOUR
T1 - Defect-rich ZnO nanosheets of high surface area as an efficient visible-light photocatalyst
AU - Wang, Jing
AU - Xia, Yi
AU - Dong, Yan
AU - Chen, Ruosong
AU - Xiang, Lan
AU - Komarneni, Sridhar
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/9/5
Y1 - 2016/9/5
N2 - A facile ultra-rapid solution method was developed to fabricate ZnO nanosheets with tunable BET surface area and rich oxygen-vacancy defects. The addition of 1 mol L-1 Na2SO4 led to an increase of BET surface area of ZnO nanosheets from 6.7 to 34.5 m2/g, through an electrostatic-controlled growth and self-assembly mechanism. Detailed analysis based on Raman scattering, room-temperature photoluminescence, X-ray photoelectron spectroscopy and electron spin resonance revealed that the as-prepared ZnO nanosheets were rich in oxygen-vacancies. Increased BET surface area led to a further increase of surface oxygen-vacancy concentration. The rich oxygen-vacancies promoted the visible-light absorption of the ZnO nanosheets, leading to high photocurrent responses and photocatalytic activities towards the degradation of rhodamine B (apparent rate constants, k = 0.0179 min-1) under visible-light illumination (λ > 420 nm), about 13 and 11 times higher, respectively than that of ZnO nanoparticles with few oxygen defects. In addition, the high-surface-area ZnO nanosheets could be effectively hybridized with Ag3PO4 nanoparticles, resulting in a further enhancement of the visible-light photocatalytic performance (k = 0.0421 min-1). This increase in performance was attributed to the increased visible-light absorption as well as the energy level matching, the latter leading to efficient charge transfer between oxygen-vacancy-rich ZnO nanosheet and Ag3PO4, suggesting a synergistic effect of surface oxygen vacancies and Ag3PO4 coupling.
AB - A facile ultra-rapid solution method was developed to fabricate ZnO nanosheets with tunable BET surface area and rich oxygen-vacancy defects. The addition of 1 mol L-1 Na2SO4 led to an increase of BET surface area of ZnO nanosheets from 6.7 to 34.5 m2/g, through an electrostatic-controlled growth and self-assembly mechanism. Detailed analysis based on Raman scattering, room-temperature photoluminescence, X-ray photoelectron spectroscopy and electron spin resonance revealed that the as-prepared ZnO nanosheets were rich in oxygen-vacancies. Increased BET surface area led to a further increase of surface oxygen-vacancy concentration. The rich oxygen-vacancies promoted the visible-light absorption of the ZnO nanosheets, leading to high photocurrent responses and photocatalytic activities towards the degradation of rhodamine B (apparent rate constants, k = 0.0179 min-1) under visible-light illumination (λ > 420 nm), about 13 and 11 times higher, respectively than that of ZnO nanoparticles with few oxygen defects. In addition, the high-surface-area ZnO nanosheets could be effectively hybridized with Ag3PO4 nanoparticles, resulting in a further enhancement of the visible-light photocatalytic performance (k = 0.0421 min-1). This increase in performance was attributed to the increased visible-light absorption as well as the energy level matching, the latter leading to efficient charge transfer between oxygen-vacancy-rich ZnO nanosheet and Ag3PO4, suggesting a synergistic effect of surface oxygen vacancies and Ag3PO4 coupling.
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U2 - 10.1016/j.apcatb.2016.03.040
DO - 10.1016/j.apcatb.2016.03.040
M3 - Article
AN - SCOPUS:84961878173
SN - 0926-3373
VL - 192
SP - 8
EP - 16
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -