Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7896
Full metadata record
DC FieldValueLanguage
dc.contributor.advisorVAIDHYANATHAN, RAMANATHAN
dc.contributor.authorJOSE, ALEENA
dc.date.accessioned2023-05-18T05:04:40Z
dc.date.available2023-05-18T05:04:40Z
dc.date.issued2023-05
dc.identifier.citation34en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7896
dc.description.abstractThe challenge of the energy crisis and the demand for clean fuels is ever-growing. Hence, hydrogen is considered the future fuel because of its clean-burning properties. Electrochemically catalyzed splitting of water provides us with a carbon-free method for producing hydrogen and oxygen. Oxygen evolution reaction (OER) has a slow kinetics which affects the overall efficiency of the process of water splitting. To overcome the OER kinetics, ruthenium and iridium-based catalysts are used, but because of their low availability, high cost and unsatisfactory stability, they are noneconomical for large-scale applications. Hence, active research is going on to develop catalysts based on cheaper transition metals for electrochemical OER. Recently, a variety of Metal-Organic Frameworks (MOFs) based OER electrocatalysts have emerged because of their highly porous nature and easy tunability of active sites. Through this work, nickel, cobalt, iron and manganese isonicotinate MOFs (Ni(4 - PyC)2, Co(4 - PyC)2, Fe(4 - PyC)2 and Mn(4 - PyC)2), and their derivatives have been synthesized, and their OER catalytic activity is studied. Electrochemical studies were done to assess the activity, kinetics and stability of these catalysts toward alkaline electrochemical OER.en_US
dc.language.isoen_USen_US
dc.subjectMetal-organic frameworksen_US
dc.subjectwater splittingen_US
dc.subjectoxygen evolution reactionen_US
dc.subjectelectrocatalystsen_US
dc.titleMetal-organic framework derived electrocatalysts for alkaline oxygen evolution reactionen_US
dc.typeThesisen_US
dc.description.embargo6 Monthsen_US
dc.type.degreeBS-MSen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20181062en_US
Appears in Collections:MS THESES

Files in This Item:
File Description SizeFormat 
20181062_Aleena_Jose_MS_Thesis.pdfMS Thesis837.59 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.