@article {46008,
	title = {Magnetic properties of sintered CoFe2O4-BaTiO3 particulate magnetoelectric composites},
	journal = {Ceramics International},
	volume = {45},
	year = {2019},
	month = {JUN},
	pages = {12307-12311},
	type = {Article},
	abstract = {<p>The magnetic properties of sintered particulate magnetoelectric CoFe2O4 - BaTiO3 composites have been studied. The particulate composites are sintered in the temperature range 1000-1300 degrees C, for a short duration of 10 min. The magnetic transition temperature (T-c) of CoFe2O4 is found to decrease with increasing the sintering temperature and sintering time, as well as on increasing the BaTiO3 content in the composites. Similarly, a reduced saturation magnetization at room temperature, compared to that expected for the CoFe2O4 content, is also observed. Powder X-ray diffraction studies showed the presence of the impurity phase related to the hexagonal ferrite BaFe12O19 in all the composites. Ba2Fe2Ti4O13 is observed as a second impurity phase in the BaTiO3 - rich composites. The present studies suggest that the composition of the piezomagnetic (CoFe2O4) phase in the CoFe2O4 - BaTiO3 magnetoelectric composite is affected during the sintering process.</p>},
	keywords = {composites, magnetic properties, Sintering},
	issn = {0272-8842},
	doi = {10.1016/j.ceramint.2019.03.145},
	author = {Mohan, S. and Joy, P. A.}
}
@article {49210,
	title = {Renewable synthesis of MoO3  nanosheets via low temperature phase transition for supercapacitor application},
	journal = {SCIENTIFIC REPORTS},
	volume = {14},
	year = {2024},
	month = {SEP },
	pages = {20503},
	type = {Journal Article},
	keywords = {alpha-MoO3, h-MoO3, Mixed phases (h and alpha) of MoO3, Renewable green synthesis, Very low temperature phase transition},
	issn = {2045-2322},
	doi = {10.1038/s41598-024-69765-x},
	author = {Sankar, K. N. Amba and Kesavan, Lokesh and Saha, Bikash and Jyolsnaraj, M. K. and Mohan, S. and Nandakumar, P. and Mohanta, Kallol and Kvarnstroem, Carita}
}
@article {49780,
	title = {Binder-free in situ interface reconstruction of NiMoO4 nanorods over Ni(OH)2 nanosheets for efficient urea oxidation},
	journal = {Advanced Sustainable Systems},
	volume = {9},
	year = {2025},
	month = {DEC},
	type = {Article},
	abstract = {<p>
	Replacing the energy-intensive oxygen evolution reaction (OER) with the urea oxidation reaction (UOR) in electrochemical water splitting offers simultaneous green hydrogen production and urea-rich wastewater oxidation, enhancing energy efficiency and economic viability. In this study, a non-noble metal-based binder-free NiMoO4/Ni(OH)2/NF electrocatalyst is developed, featuring NiMoO4 nanorods anchored on Ni(OH)2 nanosheets. This unique morphology facilitates a highly active in situ reconstructed interface, delivering a current density of 134 mA cm-2 at 1.40 V (vs RHE) in 1 m KOH with 0.33 m urea, significantly outperforming its individual components. The catalyst demonstrates excellent stability over 50 h at 30 mA cm-2. When integrated into an anion exchange membrane urea electrolyser (13 cm2 area) with Pt@C/NF as the HER cathode, the system achieves 192 mA cm-2 at 1.60 V. The post-UOR studies confirm the presence of an amorphous NiMoO4-crystalline Ni(OH)2 interface, which plays a key role in enhancing the availability of the active sites to enhance the UOR performance. The improved electrochemical performance of the engineered catalyst can be ascribed to the in situ reconstructed amorphous-crystalline interface, optimal hydrophilicity, reduced charge transfer resistance, and the distinct morphology. This strategy offers a promising pathway for developing highly active electrocatalysts for energy conversion applications.</p>
},
	keywords = {AEM, electrolyser, OWS, tomography, UOR, wastewater},
	issn = {2366-7486},
	doi = {10.1002/adsu.202500883},
	author = {Kumar, Yogesh and Barik, Sidharth and Kharabe, Geeta Pandurang and Torris, Arun and Singh, Mayank U. and Mohan, S. and Galave, Chaitanya and Tekawadia, Jyoti and Kanawade, Rajesh and Kurungot, Sreekumar}
}
