4.6 Article

Cobalt Phthalocyanine Immobilized on Graphene Oxide: An Efficient Visible-Active Catalyst for the Photoreduction of Carbon Dioxide

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 20, Issue 20, Pages 6154-6161

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201304189

Keywords

carbon dioxide reduction; cobalt; heterogeneous catalysis; photochemistry

Funding

  1. CSIR, New Delhi
  2. Analytical department of the Institute

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New graphene oxide (GO)-tethered-Co-II phthalocyanine complex [CoPc-GO] was synthesized by a stepwise procedure and demonstrated to be an efficient, cost-effective and recyclable photocatalyst for the reduction of carbon dioxide to produce methanol as the main product. The developed GO-immobilized CoPc was characterized by X-ray diffraction (XRD), FTIR, XPS, Raman, diffusion reflection UV/Vis spectroscopy, inductively coupled plasma atomic emission spectroscopy (ICP-AES), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). FTIR, XPS, Raman, UV/Vis and ICP-AES along with elemental analysis data showed that Co-II-Pc complex was successfully grafted on GO. The prepared catalyst was used for the photocatalytic reduction of carbon dioxide by using water as a solvent and triethylamine as the sacrificial donor. Methanol was obtained as the major reaction product along with the formation of minor amount of CO (0.82%). It was found that GO-grafted CoPc exhibited higher photocatalytic activity than homogeneous CoPc, as well as GO, and showed good recoverability without significant leaching during the reaction. Quantitative determination of methanol was done by GC flame-ionization detector (FID), and verification of product was done by NMR spectroscopy. The yield of methanol after 48h of reaction by using GO-CoPc catalyst in the presence of sacrificial donor triethylamine was found to be 3781.8881molg(-1)cat., and the conversion rate was found to be 78.7893molg(-1)cat.h(-1). After the photoreduction experiment, the catalyst was easily recovered by filtration and reused for the subsequent recycling experiment without significant change in the catalytic efficiency.

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