TY - JOUR
T1 - AuPd bimetallic nanoparticles decorated graphitic carbon nitride for highly efficient reduction of water to H2 under visible light irradiation
AU - Han, Changcun
AU - Wu, Linen
AU - Ge, Lei
AU - Li, Yujing
AU - Zhao, Zhen
N1 - Publisher Copyright:
© 2015 Elsevier Ltd. All rights reserved.
PY - 2015/7/22
Y1 - 2015/7/22
N2 - In this work, a new AuPd bimetallic cocatalyst decorated graphitic carbon nitride (g-C3N4) photocatalysts with high H2 evolution activity was synthesized via an in situ chemical deposition method. The physical and photophysical properties of the as-prepared AuPd/g-C3N4 were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission electron microscope (TEM), Ultraviolet-visible diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), electron spin resonance (ESR) and surface photovoltage spectroscopy (SPV). The photocatalytic H2 evolution experiments indicate that the AuPd bimetallic co-catalysts can effectively promote the separation efficiency of photo-generated charge carriers in g-C3N4, and consequently enhance the H2 evolution activity. The 0.5 wt% AuPd/g-C3N4 catalyst shows the highest catalytic activity, and corresponding H2 evolution rate is 326 μmol h-1 g-1, which are enhanced by 3.5 and 1.6 times compared with that of pristine Au/g-C3N4 and Pd/g-C3N4 under visible light irradiation. The photocatalyst can maintain photocatalytic activity after 4 cycles. A possible photocatalystic mechanism of AuPd bimetallic nanoparticles (NPs) on the enhancement of visible light performance is proposed to guide further improvement for other desirable functional materials.
AB - In this work, a new AuPd bimetallic cocatalyst decorated graphitic carbon nitride (g-C3N4) photocatalysts with high H2 evolution activity was synthesized via an in situ chemical deposition method. The physical and photophysical properties of the as-prepared AuPd/g-C3N4 were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission electron microscope (TEM), Ultraviolet-visible diffuse reflection spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), electron spin resonance (ESR) and surface photovoltage spectroscopy (SPV). The photocatalytic H2 evolution experiments indicate that the AuPd bimetallic co-catalysts can effectively promote the separation efficiency of photo-generated charge carriers in g-C3N4, and consequently enhance the H2 evolution activity. The 0.5 wt% AuPd/g-C3N4 catalyst shows the highest catalytic activity, and corresponding H2 evolution rate is 326 μmol h-1 g-1, which are enhanced by 3.5 and 1.6 times compared with that of pristine Au/g-C3N4 and Pd/g-C3N4 under visible light irradiation. The photocatalyst can maintain photocatalytic activity after 4 cycles. A possible photocatalystic mechanism of AuPd bimetallic nanoparticles (NPs) on the enhancement of visible light performance is proposed to guide further improvement for other desirable functional materials.
UR - http://www.scopus.com/inward/record.url?scp=84930207194&partnerID=8YFLogxK
U2 - 10.1016/j.carbon.2015.02.070
DO - 10.1016/j.carbon.2015.02.070
M3 - Article
AN - SCOPUS:84930207194
SN - 0008-6223
VL - 92
SP - 31
EP - 40
JO - Carbon
JF - Carbon
ER -