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M.B. Jessie Raj

Researcher at Bishop Heber College

Publications -  10
Citations -  94

M.B. Jessie Raj is an academic researcher from Bishop Heber College. The author has contributed to research in topics: Crystal & Single crystal. The author has an hindex of 3, co-authored 9 publications receiving 39 citations.

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Effect of reducing agents in tuning the third-order optical nonlinearity and optical limiting behavior of reduced graphene oxide

TL;DR: In this article, reduced graphene oxide (rGO) was prepared by reduction method using various reductants like hydrazine, sodium borohydride and ascorbic acid.
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Barium borate nanorod decorated reduced graphene oxide for optical power limiting applications

TL;DR: In this paper, the BBO:rGO nanocomposite is found to have a nonlinear refractive index almost four times higher than GO which resulted in superior optical power limiting action.
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Influence of ultrasonication time on solar light irradiated photocatalytic dye degradability and antibacterial activity of Pb doped ZnO nanocomposites

TL;DR: In this article, the synthesis of co-precipitated 5-mol% lead doped zinc oxide nanocomposites by varying ultrasonication period as 7200s, 14400s and 21600s hexagonal wurtzite structured, well defined (101) characteristic X-ray diffraction patterns of Pb/ZnO indicate that doping of lead and ultra-asonication periods significantly altered the crystallite size.
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Second and third-order NLO response of 2-amino-5-nitropyridinium tetrafluoroborate

TL;DR: Based on host-guest chemistry, a semiorganic NLO material 2-amino-5-nitropyridinium tetrafluoroborate [2A5NPFB] was synthesized and grown as single crystals as mentioned in this paper.
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Synthesis of ultrasonic assisted co-precipitated Ag/ZnO nanorods and their profound anti-liver cancer and antibacterial properties

TL;DR: In this article , an ultrasonic assisted co-precipitation method was used to synthesize silver/zinc oxide nanocomposites for potential applications in antibacterial, anti-inflammatory, anticancerous, against human liver cancer cells (hepG2).