Free-polymer controlling morphology of α-MoO 3 nanobelts by a facile hydrothermal synthesis, their electrochemistry for hydrogen evolution reactions and optical properties
Orthorhombic molybdenum oxide (α-MoO 3) nanobelts were successfully synthesized by the 100-180 °C and 2-20 h hydrothermal reactions of (NH 4) 6Mo 7O 24·4H 2O solutions containing 15 ml 2 M acid (HNO 3, H 2SO 4 or HCl) with no surfactant and template adding. These products were characterized by X-ray...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2014
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| Online Access: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84855574978&partnerID=40&md5=dc0259df40f53616cc2c2c2a289d2c6b http://cmuir.cmu.ac.th/handle/6653943832/6829 |
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| Institution: | Chiang Mai University |
| Language: | English |
| Summary: | Orthorhombic molybdenum oxide (α-MoO 3) nanobelts were successfully synthesized by the 100-180 °C and 2-20 h hydrothermal reactions of (NH 4) 6Mo 7O 24·4H 2O solutions containing 15 ml 2 M acid (HNO 3, H 2SO 4 or HCl) with no surfactant and template adding. These products were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Raman spectroscopy, and electron microscopy (EM). In the present research, the product synthesized by the 180 °C and 20 h hydrothermal reaction of the solution containing HNO 3 was α-MoO 3 nanobelts with >10 μm long and <200 nm wide. Electrochemistry for hydrogen evolution reactions (HER) and optical properties of the as-synthesized α-MoO 3 nanobelts were characterized by linear sweep voltammetry (LSV) and Tafel plot, including UV-vis and photoluminescence (PL) spectroscopy. These imply that α-MoO 3 nanobelts show satisfied performance for HER, with the 3.75 eV direct allowed band gap (E g) due to the charged transition of O 2p → Mo 4d, including the emission of 437 nm wavelength at room temperature. © 2011 Elsevier B.V. All rights reserved. |
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