Pawan Kumar1, Arvind Kumar2, B. Sreedhar3, Bir Sain1, Siddharth S. Ray2, Suman L. Jain1
1Chemical Sciences Division, CSIR‐Indian Institute of Petroleum, Mohkampur, Dehradun 248005 (India), Fax: (+91) 135‐2660202
2Analytical Sciences Division, CSIR – Indian Institute of Petroleum, Mohkampur, Dehradun 248005, India
3Inorganic and Physical Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500607, Andhra Pradesh (India)
Tóm tắt
AbstractNew graphene oxide (GO)‐tethered–CoII 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 CoII–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 48 h of reaction by using GO–CoPc catalyst in the presence of sacrificial donor triethylamine was found to be 3781.8881 μmol g−1 cat., and the conversion rate was found to be 78.7893 μmol g−1cat. 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.
