Singhal, AditiAditiSinghalBisht, AnujAnujBishtKumar, AmitAmitKumarSharma, SudhanshuSudhanshuSharma2025-08-302025-08-302016-09-0110.1016/j.jelechem.2016.07.0042-s2.0-84978275735https://d8.irins.org/handle/IITG2025/21840Nano-crystalline Co<inf>3</inf>O<inf>4</inf> is synthesized using solution combustion method. Characterization is done using XRD, TEM and BET surface area analysis. XRD shows pure nano-crystalline phase of Co<inf>3</inf>O<inf>4</inf>. Crystallinity of as prepared material improves by calcining the compound at 900 °C for 10 h while no effect is seen at 600 °C. TEM studies show that particles of around 50 nm size are formed at 400 °C. At 600 °C a well-defined hexagonal morphology could be seen both by TEM and SEM and the particle size is around 70 nm. However, TEM of the sample at 900 °C shows big agglomerates of cobalt oxide and no specific geometry could be obtained. Estimated BET surface area for the sample calcined at 600 °C is 10 m²/g. Detailed electrochemical studies are carried out in neutral and basic electrolytes where Ag/AgCl is used as the reference electrode. It is found that Co<inf>3</inf>O<inf>4</inf> is active for oxygen evolution reaction in basic medium as well as in neutral medium. KOH is used as the basic medium while KNO<inf>3</inf>, K<inf>2</inf>SO<inf>4</inf> and phosphate buffer is used for neutral medium. However, it is not active for hydrogen evolution reaction in any of the medium even at − 1.0 V. This is confirmed by gas analysis of the output gas in the cell by using a mass spectrometer. When compared with the buffer medium, it is observed that local pH changes in KNO<inf>3</inf> and K<inf>2</inf>SO<inf>4</inf> medium are possibly affecting the oxygen evolution reaction.falseCo3O4 | Electrochemistry | Hydrogen evolution | Oxygen evolution | Solution combustionArticle152-1611 September 201621arJournal20WOS:000382348100022