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The photosynthesis of methanol on 1D ordered Zn: CuInS2 nanoarraysw

  • Sung Wei Yang
  • , Guan Ting Pan
  • , Thomas C.K. Yang
  • , Chien Chung Chen
  • , Hsu Cheng Chiang

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

CO2-to-CH3OH hydrogenation reaction is one of the promising solutions not only to reduce the global warming impact by the elimination of greenhouse gases but also to produce valuable chemicals directly from carbon dioxide. In this study, pure and Zn-doped CuInS2 highly ordered nanoarrays were fabricated by the chemical bath deposition method, accompanied with the anodized aluminum oxide (AAO) arrays as a template. Structure, morphological, optical, and photoelectrochemical properties for the nanoarrays were investigated. The crystalline and morphology of the arrays were characterized by means of X-ray diffraction (XRD) and scanning electron microscope (SEM). XRD results show that main peak of CuInS2 shifts to the higher angles when the doping concentrations of Zn increase. As molar ratios of Zn in the bath solution were higher than 0.4, the semiconductor property of the sample changed from n-type to p-type from Hall measurement. The carrier densities of the Zn-doped CuInS2 arrays were found to be in the range of 1.32×1017-9.45×1020cm-3. The maximum photocurrent density was 2.02mA/cm2 for the p-type CuInS2 arrays with Zn-doped molar ratios of 0.4. Time-dependent solid phase reactions were monitored by the diffuse reflectance infrared Fourier transform spectroscopy (DRIFT). Additionally, the quadrupole mass spectroscopy (MS) accompanied with gas chromatograph (GC) was used for the gas phase analysis. The maximal methanol production rate during the photocatalysis was found to be 0.032M/h, which is better than that of the referenced CBD film (0.003M/h) prepared in the same compositions.

Original languageEnglish
Pages (from-to)1509-1515
Number of pages7
JournalJournal of the Taiwan Institute of Chemical Engineers
Volume45
Issue number4
DOIs
StatePublished - Jul 2014

Bibliographical note

Funding Information:
The partial financial support from the National Science Council of ROC (NSC 101-2221-E-027-023 ) is gratefully appreciated. The authors would also like to thank the financial support from National Taipei University of Technology – Taipei Medical University Joint Research (NTUT-TMU 101-21).

Keywords

  • Photocatalysis
  • Photochemical performance

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