Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair. Issue 10 (17th December 2018)
- Record Type:
- Journal Article
- Title:
- Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair. Issue 10 (17th December 2018)
- Main Title:
- Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair
- Authors:
- Yu, Yang
He, Teng
Wu, Anan
Pei, Qijun
Karkamkar, Abhijeet
Autrey, Tom
Chen, Ping - Abstract:
- Abstract: Hydrogen uptake and release in arene–cycloalkane pairs provide an attractive opportunity for on‐board and off‐board hydrogen storage. However, the efficiency of arene–cycloalkane pairs currently is limited by unfavorable thermodynamics for hydrogen release. It is shown here that the thermodynamics can be optimized by replacement of H in the ‐OH group of cyclohexanol and phenol with alkali or alkaline earth metals. The enthalpy change upon dehydrogenation decreases substantially, which correlates with the delocalization of the oxygen electron to the benzene ring in phenoxides. Theoretical calculations reveal that replacement of H with a metal leads to a reduction of the HOMO–LUMO energy gap and elongation of the C−H bond in the α site in cyclohexanolate, which indicates that the cyclohexanol is activated upon metal substitution. The experimental results demonstrate that sodium phenoxide–cyclohexanolate, an air‐ and water‐stable pair, can desorb hydrogen at ca. 413 K and 373 K in the solid form and in an aqueous solution, respectively. Hydrogenation, on the other hand, is accomplished at temperatures as low as 303 K. Abstract : Optimized storage : The metalation of the phenoxide–cyclohexanolate pair is a successful strategy to optimize the thermodynamic properties of this type of hydrogen storage material (see figure). In experiments the sodiated pair desorbed hydrogen at 413 K (373 K) in the solid state (aqueous solution), whereas hydrogenation could be accomplishedAbstract: Hydrogen uptake and release in arene–cycloalkane pairs provide an attractive opportunity for on‐board and off‐board hydrogen storage. However, the efficiency of arene–cycloalkane pairs currently is limited by unfavorable thermodynamics for hydrogen release. It is shown here that the thermodynamics can be optimized by replacement of H in the ‐OH group of cyclohexanol and phenol with alkali or alkaline earth metals. The enthalpy change upon dehydrogenation decreases substantially, which correlates with the delocalization of the oxygen electron to the benzene ring in phenoxides. Theoretical calculations reveal that replacement of H with a metal leads to a reduction of the HOMO–LUMO energy gap and elongation of the C−H bond in the α site in cyclohexanolate, which indicates that the cyclohexanol is activated upon metal substitution. The experimental results demonstrate that sodium phenoxide–cyclohexanolate, an air‐ and water‐stable pair, can desorb hydrogen at ca. 413 K and 373 K in the solid form and in an aqueous solution, respectively. Hydrogenation, on the other hand, is accomplished at temperatures as low as 303 K. Abstract : Optimized storage : The metalation of the phenoxide–cyclohexanolate pair is a successful strategy to optimize the thermodynamic properties of this type of hydrogen storage material (see figure). In experiments the sodiated pair desorbed hydrogen at 413 K (373 K) in the solid state (aqueous solution), whereas hydrogenation could be accomplished at temperatures as low as 202 K. … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 58:Issue 10(2019)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 58:Issue 10(2019)
- Issue Display:
- Volume 58, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 58
- Issue:
- 10
- Issue Sort Value:
- 2019-0058-0010-0000
- Page Start:
- 3102
- Page End:
- 3107
- Publication Date:
- 2018-12-17
- Subjects:
- hydrogen storage materials -- metalation -- organic hydrides -- thermodynamic modification
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201810945 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11742.xml