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Molecules
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Catalysis for Energy Storage and CO2 Conversion
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Catalysis for Energy Storage and CO2 Conversion

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Green Chemistry".

Deadline for manuscript submissions: closed (30 April 2019) | Viewed by 6616

Special Issue Editor

Prof. Dr. Carlo Nervi

E-Mail Website
Guest Editor
1. Department of Chemistry and NIS (Centre of Excellence), University of Turin, Via P. Giuria 7, 10125 Torino, Italy
2. CIRCC, Via Celso Ulpiani 27, 70126 Bari, Italy
Interests: inorganic electrochemistry; organometallic compounds; catalysts and electrocatalysts for energy and CO2 conversion; water splitting; DFT calculations; energy storage

Special Issue Information

Dear Colleagues,

The Special Issue is focused on a hot topic, namely the catalytic conversion of CO2 in chemically-useful products, as well as chemical approaches that will provide a renewable (green) energy source in order to mitigate CO2 emissions.

The continued release of huge amounts of carbon dioxide into the atmosphere by human activities raises several environmental concerns. CO2 emissions are strictly connected with the worldwide energy demand and the consumption and depletion of non-renewable fossil fuels. While Carbon Capture and Storage (CCS) could be a short-term environmental approach, a wise long-term solution must be undoubtedly developed. An efficient way to transform CO2 in useful chemicals and/or fuel precursors, adopting renewable green energies, would represents a perfect goal in mitigating two of the most important problems that our society is facing.

Worldwide researchers working in the field, are cordially invited to contribute with original research papers or reviews to this Special Issue of Molecules, which is dealing with the design, synthesis, and evaluation of novel catalysts/methods for efficient energy storage and CO2 conversion.

Prof. Dr. Carlo Nervi
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Electrochemical CO2 reduction
  • Chemical CO2 reduction
  • Photochemical CO2 reduction
  • Electrocatalysis for CO2 reduction
  • Photoelectrochemical Cells
  • Water Splitting
  • Efficient Energy Storage
  • Renewable Hydrogen Production

Published Papers (2 papers)

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Research

10 pages, 6930 KiB  
Article
Cu(I)/Ionic Liquids Promote the Conversion of Carbon Dioxide into Oxazolidinones at Room Temperature
by Jikuan Qiu, Yue Zhao, Yuling Zhao, Huiyong Wang, Zhiyong Li, Jianji Wang and Tiantian Jiao
Molecules 2019, 24(7), 1241; https://doi.org/10.3390/molecules24071241 - 29 Mar 2019
Cited by 12 | Viewed by 2859
Abstract
Recently, the efficient chemical fixation of carbon dioxide (CO2) into high value chemicals without using noble metal catalysts has become extremely appealing from the viewpoint of sustainable chemistry. In this work, a one-pot three component reaction of propargylic alcohols, anines and [...] Read more.
Recently, the efficient chemical fixation of carbon dioxide (CO2) into high value chemicals without using noble metal catalysts has become extremely appealing from the viewpoint of sustainable chemistry. In this work, a one-pot three component reaction of propargylic alcohols, anines and CO2 that can proceed in an atom economy and environmentally benign manner by combination of CuI and tetrabutylphosphonium imidazol ([P4444][Im]) as a catalyst was described. Catalysis studies indicate that this catalytic system is an effective catalyst for the conversion of CO2 into oxazolidinones at room temperature and ambient pressure without any solvent. The results provide a useful way to design novel noble metal-free catalyst systems for the transformation of CO2 into other valuable compounds. Full article
(This article belongs to the Special Issue Catalysis for Energy Storage and CO2 Conversion)
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20 pages, 4400 KiB  
Article
Study of Catalytic CO2 Absorption and Desorption with Tertiary Amine DEEA and 1DMA-2P with the Aid of Solid Acid and Solid Alkaline Chemicals
by Huancong Shi, Min Huang, Qiming Wu, Linna Zheng, Lifeng Cui, Shuping Zhang and Paitoon Tontiwachwuthikul
Molecules 2019, 24(6), 1009; https://doi.org/10.3390/molecules24061009 - 13 Mar 2019
Cited by 10 | Viewed by 3443
Abstract
Studies of catalytic CO2 absorption and desorption were completed in two well-performed tertiary amines: diethylmonoethanolamine (DEEA) and 1-dimethylamino-2-propanol (1DMA-2P), with the aid of CaCO3 and MgCO3 in the absorption process, and with the aid of γ-Al2O3 and [...] Read more.
Studies of catalytic CO2 absorption and desorption were completed in two well-performed tertiary amines: diethylmonoethanolamine (DEEA) and 1-dimethylamino-2-propanol (1DMA-2P), with the aid of CaCO3 and MgCO3 in the absorption process, and with the aid of γ-Al2O3 and H-ZSM-5 in the desorption process. The batch process was used for CO2 absorption with solid alkalis, and the recirculation process was used for CO2 desorption with solid acid catalysts. The CO2 equilibrium solubility and pKa were also measured at 293 K with results comparable to the literature. The catalytic tests discovered that the heterogeneous catalysis of tertiary amines on both absorption and desorption sides were quite different from monoethanolamine (MEA) and diethanolamine (DEA). These results were illustrative as a start-up to further study of the kinetics of heterogeneous catalysis of CO2 to tertiary amines based on their special reaction schemes and base-catalyzed hydration mechanism. Full article
(This article belongs to the Special Issue Catalysis for Energy Storage and CO2 Conversion)
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