Bisht, AnujAnujBishtGangwar, Bhanu P.Bhanu P.GangwarAnupriya, T.T.AnupriyaSharma, SudhanshuSudhanshuSharma2025-09-012025-09-012014-01-0110.1007/s10008-013-2252-72-s2.0-84891843412http://repository.iitgn.ac.in/handle/IITG2025/29325Pt supported over CeO<inf>2</inf> (Pt on CeO<inf>2</inf>) and Pt doped CeO<inf>2</inf> (Pt in CeO<inf>2</inf>) are synthesized using chemical reduction and solution combustion method. In chemical reduction two different reducing agents are used namely; hydrazine hydrate and formaldehyde giving Pt supported over CeO<inf>2</inf>. Solution combustion method is used to prepare Pt doped CeO<inf>2</inf>. Detailed characterization using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area measurement and transmission electron microscopy (TEM) is carried out to distinguish the Pt supported and doped compounds. XRD and TEM results have clearly shown the differences in the structure and morphology, however, BET results do not show significant differences. Further, electrochemical measurements are performed in neutral medium to differentiate the electrochemical activity. Cyclic voltammetry (CV) indeed shows noticeable differences between Pt supported over CeO<inf>2</inf> and Pt doped CeO<inf>2</inf>. CeO<inf>2</inf> alone has also shown different electrochemical behavior compared to the Pt containing CeO<inf>2</inf>. Considering oxygen evolution reaction (OER) as a model reaction, Tafel slope measurements are performed for CeO<inf>2</inf>, Pt supported over CeO <inf>2</inf> and Pt doped CeO<inf>2</inf> to observe the differences. It was noted that CeO<inf>2</inf> and Pt doped CeO<inf>2</inf> showed similar Tafel slope indicating the same mechanism, while Pt supported over CeO<inf>2</inf> showed different Tafel slopes, hence the different mechanism. © 2013 Springer-Verlag Berlin Heidelberg.falseChemical reduction | Electrochemical properties | Interaction | Oxygen evolution reaction | TafelUnderstanding the electrochemical differences of Pt doped and Pt supported over CeO2Article197-206January 201421arJournal21WOS:000329105400024