Please use this identifier to cite or link to this item:
https://libjncir.jncasr.ac.in/xmlui/handle/10572/2092
Title: | Hydrazine as a hydrogen carrier in the photocatalytic generation of H-2 using CdS quantum dots |
Authors: | Jana, Manoj K. Gupta, Uttam Rao, C. N. R. |
Keywords: | Chemistry Colloidal Nanocrystals Surface Ligands Solar-Cells Storage Nickel Decomposition Efficiency Catalysts |
Issue Date: | 2016 |
Publisher: | Royal Society of Chemistry |
Citation: | Jana, M. K.; Gupta, U.; Rao, C. N. R., Hydrazine as a hydrogen carrier in the photocatalytic generation of H-2 using CdS quantum dots. Dalton Transactions 2016, 45 (38), 15137-15141 http://dx.doi.org/10.1039/c6dt02505f Dalton Transactions 45 38 |
Abstract: | The compelling need for safe storage and transportation of H-2 has made liquid-phase materials safer H-2-carriers with a high gravimetric and volumetric hydrogen density. Unlike thermal or electrocatalytic decomposition on precious metal catalysts, a photocatalytic route to decomposing these liquid-phase materials can offer triggered onboard production of H-2 and help mitigate the safety issues concerned with H-2 storage. We have investigated visible-light induced H-2 evolution from aqueous hydrazine using CdS quantum dots (QDs) as metal-free photocatalysts. Hydrazine acts as a H-2 carrier as well as a donor, giving rise to a visible-light induced H-2 evolution activity as high as 33 mmol h(-1) g(-1) at pH 8. This has been achieved by the use of CdS QDs capped with S2- ligands. The use of larger ligands such as mercaptopropionic acid hinders the adsorption of hydrazine onto CdS QDs and significantly decreases the activity. The effect of pH on the hydrogen yield in aqueous hydrazine has also been examined. |
Description: | Restricted Access |
URI: | https://libjncir.jncasr.ac.in/xmlui/10572/2092 |
ISSN: | 1477-9226 |
Appears in Collections: | Research Papers (Prof. C.N.R. Rao) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
105.pdf Restricted Access | 1.95 MB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.