Synthesis and Characterization of Oxygen Vacancy Induced Narrow Bandgap Tungsten Oxide (WO3-x) Nanoparticles by Plasma Discharge in Liquid and Its Photocatalytic Activity

被引:112
作者
Boruah, Palash Jyoti [1 ]
Khanikar, Rakesh Ruchel [1 ]
Bailung, H. [1 ]
机构
[1] Inst Adv Study Sci & Technol, Phys Sci Div, Plasma Applicat Lab, Garchuk 781035, Guwahati, India
关键词
In-liquid plasma; Nanoparticles; Oxygen vacancy; Narrow bandgap; Photocatalytic efficiency; ARC-DISCHARGE; ELECTROCHEMICAL PERFORMANCE; ELECTRICAL DISCHARGES; GOLD NANOPARTICLES; AMORPHOUS WO3; PARTICLE-SIZE; SILVER; TRANSITION; TRIOXIDE; FABRICATION;
D O I
10.1007/s11090-020-10073-3
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Narrow bandgap tungsten oxide (WO3-x) nanoparticles have been synthesized by single-step plasma discharge in deionized water between two vertically pointed tungsten electrodes. Bombardment of energetic electrons on the as-formed nanoparticles in the plasma zone creates defect states. Formation of electron-rich oxygen vacancies on the crystal planes and grain boundary defects have been investigated. The peak shift and broadening in the Raman and FTIR spectra indicate the formation of oxygen vacancies and sub-stoichiometric WO3 nanoparticles. EDX analysis provides the ratio of tungsten to oxygen to be around 1:2.4. Optical bandgap has been found to be 2.15 eV, which is less than the bulk value of 2.54 eV. Observation of higher amount of defect states from TEM and XPS provides the reason for the formation of narrow bandgap tungsten oxide nanoparticles. The photocatalytic efficiency of the plasma synthesize WO3-x nanoparticles is found to be higher than that of commercial bulk and nano WO3 particles.
引用
收藏
页码:1019 / 1036
页数:18
相关论文
共 77 条
[1]   Pristine simple oxides as visible light driven photocatalysts: Highly efficient decomposition of organic compounds over platinum-loaded tungsten oxide [J].
Abe, Ryu ;
Takami, Hiticishi ;
Murakami, Naoya ;
Ohtani, Bunsho .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (25) :7780-+
[2]   Photo-catalytic Killing of HeLa Cancer Cells Using Facile Synthesized Pure and Ag Loaded WO3 Nanoparticles [J].
AbuMousa, Rasha A. ;
Baig, Umair ;
Gondal, Mohammed A. ;
AlSalhi, Mohamad S. ;
Alqahtani, Fulwah Yahya ;
Akhtar, Sultan ;
Aleanizy, Fadilah Sfouq ;
Dastageer, Mohamed A. .
SCIENTIFIC REPORTS, 2018, 8
[3]  
Ahmed MW, 2017, APPL SCI CONVERG TEC, V26, P118
[4]   Role of synthesis method and particle size of nanostructured TiO2 on its photoactivity [J].
Almquist, CB ;
Biswas, P .
JOURNAL OF CATALYSIS, 2002, 212 (02) :145-156
[5]   RAMAN STUDY OF CERAMIC TUNGSTEN TRIOXIDE AT LOW-TEMPERATURES [J].
ANDERSON, A .
SPECTROSCOPY LETTERS, 1976, 9 (11) :809-819
[6]   Oxygen vacancy induced band gap narrowing of ZnO nanostructures by an electrochemically active biofilm [J].
Ansari, Sajid Ali ;
Khan, Mohammad Mansoob ;
Kalathil, Shafeer ;
Nisar, Ambreen ;
Lee, Jintae ;
Cho, Moo Hwan .
NANOSCALE, 2013, 5 (19) :9238-9246
[7]   Synthesis and photocatalytic activity of WO3 nanoparticles prepared by the arc discharge method in deionized water [J].
Ashkarran, A. A. ;
zad, A. Iraji ;
Ahadian, M. M. ;
Ardakani, S. A. Mahdavi .
NANOTECHNOLOGY, 2008, 19 (19)
[8]   A facile one-step fabrication of novel WO3/Fe2(WO4)3•10.7H2O porous microplates with remarkable photocatalytic activities [J].
Aslam, Imran ;
Cao, Chuanbao ;
Tanveer, M. ;
Farooq, M. Hassan ;
Tahir, Muhammad ;
Khalid, Syed ;
Khan, Waheed S. ;
Idrees, Faryal ;
Rizwan, Muhammad ;
Butt, Faheem K. .
CRYSTENGCOMM, 2015, 17 (26) :4809-4817
[9]   The visible light induced photocatalytic activity of tungsten trioxide powders [J].
Bamwenda, GR ;
Arakawa, H .
APPLIED CATALYSIS A-GENERAL, 2001, 210 (1-2) :181-191
[10]   Visible Light Photocatalysis with c-WO3-x/WO3xH2O Nanoheterostructures In Situ Formed in Mesoporous Polycarbosilane-Siloxane Polymer [J].
Bazarjani, Mahdi Seifollahi ;
Hojamberdiev, Mirabbos ;
Morita, Koji ;
Zhu, Gangqiang ;
Cherkashinin, Gennady ;
Fasel, Claudia ;
Herrmann, Thomas ;
Breitzke, Hergen ;
Gurlo, Aleksander ;
Riedel, Ralf .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (11) :4467-4475