Copper(II) imidazolate frameworks as highly efficient photocatalysts for reduction of CO2 into methanol under visible light irradiation
Description
Three copper(II) imidazolate frameworks were synthesized by a hydrothermal (or precipitation) reaction. The catalysts were characterized by X-ray diffraction (XRD), nitrogen adsorption, transmission electron microscopy (TEM), ultraviolet–visible spectroscopy (UV–vis), Fourier transform infrared spectra (FTIR), thermogravimetry (TG). Meanwhile, the photocatalytic activities of the samples for reduction of CO2 into methanol and degradation of methylene blue (MB) under visible light irradiation were also investigated. The results show that the as-prepared samples exhibit better photocatalytic activities for the reduction of carbon dioxide into methanol with water and degradation of MB under visible light irradiation. The orthorhombic copper(II) imidazolate frameworks with a band gap of 2.49 eV and green (G) color has the best photocatalytic activity for reduction of CO2 into methanol, 1712.7 μmol/g over 5 h, which is about three times as large as that of monoclinic copper(II) imidazolate frameworks with a band gap 2.70 eV and blue (J) color. The degradation kinetics of MB over three photocatalysts fitted well to the apparent first-order rate equation and the apparent rate constants for the degradation of MB over G, J and P (with pink color) are 0.0038, 0.0013 and 0.0016 min−1, respectively. The synergistic effects of smallest band gap and orthorhombic crystal phase structure are the critical factors for the better photocatalytic activities of G. Moreover, three frameworks can also be stable up to 250 °C. The investigation of Cu-based zeolitic imidazolate frameworks maybe provide a design strategy for a new class of photocatalysts applied in degradation of contaminations, reduction of CO2, and even water splitting into hydrogen and oxygen under visible light. - Graphical abstract: Carbon dioxide was reduced into methanol with water over copper(II) imidazolate frameworks under visible light irradiation. - Highlights: • Three copper(II) imidazolate frameworks were first applied in the photo-reduction of CO2. • The photocatalytic activities of the frameworks depend on their band gap and phase structures. • The photocatalytic activity of orthorhombic frameworks is 3 times that of monoclinic frameworks. • The degradation kinetics of MB over three photocatalysts followed the first-order rate equation. • The largest yield for reduction of CO2 into methanol on green framworks was 1712.7 μmol/g over 5 h
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jssc.2013.04.016Additional details
Identifiers
- DOI
- 10.1016/j.jssc.2013.04.016;
- PII
- S0022-4596(13)00210-7;
Publishing Information
- Journal Title
- Journal of Solid State Chemistry
- Journal Volume
- 203
- Journal Page Range
- p. 154-159
- ISSN
- 0022-4596
- CODEN
- JSSCBI
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46015203
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADSORPTION; CARBON DIOXIDE; CATALYSTS; CONTAMINATION; CRYSTALS; FOURIER TRANSFORMATION; INFRARED SPECTRA; IRRADIATION; METHANOL; MONOCLINIC LATTICES; ORTHORHOMBIC LATTICES; PHOTOCATALYSIS; PRECIPITATION; REACTION KINETICS; SPECTROSCOPY; THERMAL GRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION; ZEOLITES
- Descriptors DEC
- ALCOHOLS; CARBON COMPOUNDS; CARBON OXIDES; CATALYSIS; CHALCOGENIDES; CHEMICAL ANALYSIS; COHERENT SCATTERING; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIFFRACTION; ELECTRON MICROSCOPY; GRAVIMETRIC ANALYSIS; HYDROXY COMPOUNDS; INORGANIC ION EXCHANGERS; INTEGRAL TRANSFORMATIONS; ION EXCHANGE MATERIALS; KINETICS; MATERIALS; MICROSCOPY; MINERALS; ORGANIC COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SEPARATION PROCESSES; SILICATE MINERALS; SORPTION; SPECTRA; THERMAL ANALYSIS; TRANSFORMATIONS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.