Comprehensive Study of All-Solid-State Z-Scheme Photocatalytic Systems of ZnO/Pt/CdZnS

被引:46
作者
Isimjan, Tayirjan Taylor [1 ]
Maity, Partha [2 ]
Llorca, Jordi [3 ,4 ]
Ahmed, Toseef [5 ]
Parida, Manas R. [2 ]
Mohammed, Omar F. [2 ]
Idriss, Hicham [1 ]
机构
[1] KAUST, SABIC CRD, Fundamental Catalysis, Thuwal 239556900, Saudi Arabia
[2] KAUST, Solar Ctr, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia
[3] Tech Univ Catalonia, EEBE, Inst Energy Technol, Dept Chem Engn, Barcelona 08930, Spain
[4] Tech Univ Catalonia, EEBE, Barcelona Res Ctr Multiscale Sci & Engn, Barcelona 08930, Spain
[5] SABIC Technol Ctr, Riyadh 11422, Saudi Arabia
关键词
ELECTRON-HOLE RECOMBINATION; HYDROGEN GENERATION; EXCITON DYNAMICS; WATER; CDS; EVOLUTION; ENERGY; HETEROSTRUCTURE; HETEROJUNCTION; SEMICONDUCTORS;
D O I
10.1021/acsomega.7b00767
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have investigated a Z-scheme based on a ZnO/Pt/CdZnS photocatalyst, active in the presence of a complex medium composed of acetic acid and benzyl alcohol, the effects of which on the catalyst stability and performance are studied. Transmission electron microscopy images showed uniformly dispersed sub-nanometer Pt particles. Inductively coupled plasma and X-ray photoelectron spectroscopy analyses suggested that Pt is sandwiched between ZnO and CdZnS. An apparent quantum yield (AQY) of 34% was obtained over the [ZnO] 4/1 wt % Pt/CdZnS system at 360 nm, 2.5-fold higher than that of 1% Pt/CdZnS (14%). Furthermore, an AQY of 16% was observed using [ZnO] 4/1 wt % Pt/ CdZnS, which was comparable to that of 1 wt % Pt/CdZnS (10%) at 460 nm. On the basis of these results, we proposed a charge transfer mechanism, which was confirmed through femtosecond transient absorption spectroscopy. Finally, we identified the two main factors that affected the stability of the catalyst, which were the sacrificial reagent and the acidic pH.
引用
收藏
页码:4828 / 4837
页数:10
相关论文
共 38 条
[1]   XPS analysis of p-type Cu-doped CdS thin films [J].
Abe, T ;
Kashiwaba, Y ;
Baba, M ;
Imai, J ;
Sasaki, H .
APPLIED SURFACE SCIENCE, 2001, 175 :549-554
[2]   Adsorption of water on thin V2O3(0001) films [J].
Abu Haija, M ;
Guimond, S ;
Uhl, A ;
Kuhlenbeck, H ;
Freund, HJ .
SURFACE SCIENCE, 2006, 600 (05) :1040-1047
[3]   ARTIFICIAL PHOTOSYNTHESIS - SOLAR SPLITTING OF WATER TO HYDROGEN AND OXYGEN [J].
BARD, AJ ;
FOX, MA .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (03) :141-145
[4]   Effect of Surface Coating on the Photocatalytic Function of Hybrid CdS-Au Nanorods [J].
Ben-Shahar, Yuval ;
Scotognella, Francesco ;
Waiskopf, Nir ;
Kriegel, Ilka ;
Dal Conte, Stefano ;
Cerullo, Giulio ;
Banin, Uri .
SMALL, 2015, 11 (04) :462-471
[5]   Exciton Dynamics of CdS Thin Films Produced by Chemical Bath Deposition and DC Pulse Sputtering [J].
Cooper, Jason K. ;
Cao, Jinbo ;
Zhang, Jin Z. .
ACS APPLIED MATERIALS & INTERFACES, 2013, 5 (15) :7544-7551
[6]   Surface chemical analysis and electrokinetic properties of synthetic spherical mixed zinc-cadmium sulfides [J].
Duran, JDG ;
Guindo, MC ;
Delgado, AV ;
GonzalezCaballero, F .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 193 (02) :223-233
[7]   Real-Time Observation of Ultrafast Intraband Relaxation and Exciton Multiplication in PbS Quantum Dots [J].
El-Ballouli, Ala'a O. ;
Alarousu, Erkki ;
Usman, Anwar ;
Pan, Jun ;
Bakr, Osman M. ;
Mohammed, Omar F. .
ACS PHOTONICS, 2014, 1 (03) :285-292
[8]   Effect of Dot Size on Exciton Binding Energy and Electron-Hole Recombination Probability in CdSe Quantum Dots [J].
Elward, Jennifer M. ;
Chakraborty, Arindam .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2013, 9 (10) :4351-4359
[9]   XPS and FTIR surface characterization of TiO2 particles used in polymer encapsulation [J].
Erdem, B ;
Hunsicker, RA ;
Simmons, GW ;
Sudol, ED ;
Dimonie, VL ;
El-Aasser, MS .
LANGMUIR, 2001, 17 (09) :2664-2669
[10]   Preparation of 1D cubic Cd0.8Zn0.2S solid-solution nanowires using levelling effect of TGA and improved photocatalytic H2-production activity [J].
Han, Zhonghui ;
Chen, Gang ;
Li, Chunmei ;
Yu, Yaoguang ;
Zhou, Yansong .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (04) :1696-1702