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

光催化 催化作用 三乙胺 热重分析 拉曼光谱 石墨烯 扫描电子显微镜 核化学 X射线光电子能谱 傅里叶变换红外光谱 甲醇 材料科学 化学 无机化学 有机化学 化学工程 纳米技术 光学 物理 工程类 复合材料
作者
Pawan Kumar,Arvind Kumar,B. Sreedhar,Bir Sain,Siddharth S. Ray,Suman L. Jain
出处
期刊:Chemistry: A European Journal [Wiley]
卷期号:20 (20): 6154-6161 被引量:146
标识
DOI:10.1002/chem.201304189
摘要

Abstract 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 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 −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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