Krishnamurthi Muralidharan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Krishnamurthi Muralidharan has a total of 85 co-authors. Here are the top co-authors by number of shared publications:
Manzoor Ahmad Pandit
School of Chemistry, University of Hyderabad, Hyderabad 500046, India; Materials Genome Institute, Shanghai University, Shanghai 200444, China
10 shared publications- Billakanti Srinivas
University of Hyderabad
8 shared publications - Anuj A. Vargeese
Laboratory for Energetic and Energy Materials Research, Department of Chemistry, National Institute of Technology Calicut (NITC), NIT Campus P. O., Calicut, Kerala, 673601, India
6 shared publications Baskaran Ganesh Kumar
6 shared publications- Dasari Sai Hemanth Kumar
School of Chemistry, University of Hyderabad, Hyderabad 500046, Telangana, India
6 shared publications Heeralal Vignesh Babu
School of Chemistry, University of Hyderabad, Hyderabad 500 046, India
6 shared publications
Latest Publications
- Open Access
- 12 March 2026
- Published by Royal Society of Chemistry (RSC) in RSC Applied Polymers
- Vol. 4 (3) , 1086-1099
Low band gap π-conjugated porous polymers as bifunctional photoelectrocatalysts for overall water splitting
We have used conjugated microporous polymers (CMPs) as bifunctional catalyst for HER/OER/OWSR.
- 12 March 2026
- Published by Royal Society of Chemistry (RSC) in RSC Applied Polymers
- Vol. 4 (3) , 1086-1099
Open AccessLow band gap π-conjugated porous polymers as bifunctional photoelectrocatalysts for overall water splitting
We have used conjugated microporous polymers (CMPs) as bifunctional catalyst for HER/OER/OWSR.
- Open Access
- 29 May 2025
- Published by MDPI AG in Journal of Composites Science
- Vol. 9 (6) , 277
Epoxy Resins and Their Hardeners Based on Phosphorus–Nitrogen Compounds
This review examines the fire-retardant properties of compositions that incorporate various classes of phosphorus–nitrogen compounds. Specifically, it focuses on nitrogen-containing derivatives of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, phosphinates, phosphorus–nitrogen salts, and aryloxycyclophosphazenes. The findings indicate that these classes of fire retardants enhance the limiting oxygen index, decrease heat and smoke emission indices in epoxy compositions, and facilitate the creation of self-extinguishing materials. Notably, aryloxycyclophosphazenes with reactive functional groups emerge as the most effective fire retardants, particularly in terms of their impact on the mechanical properties of epoxy compositions and compatibility with epoxy resin. This review would be a valuable resource for engineers, chemical engineers, materials scientists, and researchers engaged in the development of non-combustible polymer composites and organoelement compounds.
- 29 May 2025
- Published by MDPI AG in Journal of Composites Science
- Vol. 9 (6) , 277
Open AccessEpoxy Resins and Their Hardeners Based on Phosphorus–Nitrogen Compounds
This review examines the fire-retardant properties of compositions that incorporate various classes of phosphorus–nitrogen compounds. Specifically, it focuses on nitrogen-containing derivatives of 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, phosphinates, phosphorus–nitrogen salts, and aryloxycyclophosphazenes. The findings indicate that these classes of fire retardants enhance the limiting oxygen index, decrease heat and smoke emission indices in epoxy compositions, and facilitate the creation of self-extinguishing materials. Notably, aryloxycyclophosphazenes with reactive functional groups emerge as the most effective fire retardants, particularly in terms of their impact on the mechanical properties of epoxy compositions and compatibility with epoxy resin. This review would be a valuable resource for engineers, chemical engineers, materials scientists, and researchers engaged in the development of non-combustible polymer composites and organoelement compounds.
- 27 April 2025
- Published by Elsevier in Journal of Environmental Sciences
- Vol. 161, 686-696
Hierarchical porous CuFe-MOF nanostructures as dual electrocatalyst for hydrogen evolution reaction and nitrate reduction reaction
- 27 April 2025
- Published by Elsevier in Journal of Environmental Sciences
- Vol. 161, 686-696
Hierarchical porous CuFe-MOF nanostructures as dual electrocatalyst for hydrogen evolution reaction and nitrate reduction reaction
- 21 April 2025
- Published by Springer Nature in Journal of Solid State Electrochemistry
- Vol. 29 (10) , 4461-4471
Organic-free NiSe2, CoSe2, and NiSe2/CoSe2 for non-enzymatic glucose sensing
- 21 April 2025
- Published by Springer Nature in Journal of Solid State Electrochemistry
- Vol. 29 (10) , 4461-4471
Organic-free NiSe2, CoSe2, and NiSe2/CoSe2 for non-enzymatic glucose sensing
- Open Access
- 10 March 2025
- Published by Royal Society of Chemistry (RSC) in RSC Applied Interfaces
- Vol. 2 (3) , 780-794
B,N co-doped V2C nanoparticle embedded FeP nanoflake substrates as unique bifunctional electrocatalysts for overall water splitting in alkaline media
Hydrogen energy as a solution to meet energy demands has highlighted the need for efficient and cost-effective electrocatalysts for hydrogen production through water electrolysis.
- 10 March 2025
- Published by Royal Society of Chemistry (RSC) in RSC Applied Interfaces
- Vol. 2 (3) , 780-794
Open AccessB,N co-doped V2C nanoparticle embedded FeP nanoflake substrates as unique bifunctional electrocatalysts for overall water splitting in alkaline media
Hydrogen energy as a solution to meet energy demands has highlighted the need for efficient and cost-effective electrocatalysts for hydrogen production through water electrolysis.
- Open Access
- 20 December 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (4) , 1143-1153
Morphology controlled Cu3BiS3 nanostructures: superior electrocatalytic sensing of organic nitro compounds
Addressing the pressing need to develop affordable and efficient catalysts is essential.
- 20 December 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (4) , 1143-1153
Open AccessMorphology controlled Cu3BiS3 nanostructures: superior electrocatalytic sensing of organic nitro compounds
Addressing the pressing need to develop affordable and efficient catalysts is essential.
- 4 September 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (18) , 17878-17890
NiSe Nanoparticles Embedded Bimetallic MoCo Nanoflakes as an Effective Bifunctional Electrocatalyst for Water Splitting
- 4 September 2024
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 38 (18) , 17878-17890
NiSe Nanoparticles Embedded Bimetallic MoCo Nanoflakes as an Effective Bifunctional Electrocatalyst for Water Splitting
- 17 April 2024
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 53 (20) , 8593-8603
Single-step synthesis of ternary metal chalcogenides (sf-CuInS2 and sf-CuInSe2) stripped off the organic cover and their use as a catalyst for symmetric Glaser–Hay coupling reactions
Generally, inorganic nano/microparticles produced by chemical routes are covered by organic surfactants or polymers to control their agglomeration during their synthesis. However, these surfactants and polymers negatively affect their catalytic activity because these molecules mask the surface. This work presents the synthesis of surfactant-free CuInS2 and CuInSe2 (sf-CuInS2 and sf-CuInSe2) nano/microparticles through simple reactions without surfactant or polymer coatings using LiBH4 under a thermodynamically favourable condition. These reactions are rare observations of a single-step process to produce ternary metal chalcogenides without any template assistance. We have also demonstrated efficient catalysis by sf-CuInS2 nanoparticles in the coupling reaction of substituted phenylacetylenes. We tested it as catalysts in dimerizing 1,3-diyne derivatives while using 8-diazabicyclo[5.4.0]undec-7-ene (DBU) as the base. These Glassar–Hay coupling reactions are conducted at room temperature in acetonitrile (4–7 h, depending on the substrate) using 10 mg of sf-CuInS2. The maximum yield obtained in these reactions is 97%, while the catalyst is reusable for five cycles with little difference in its ability to catalyse. The effectiveness of the catalyst is credited to the availability of a free catalytic surface.
- 17 April 2024
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 53 (20) , 8593-8603
Single-step synthesis of ternary metal chalcogenides (sf-CuInS2 and sf-CuInSe2) stripped off the organic cover and their use as a catalyst for symmetric Glaser–Hay coupling reactions
Generally, inorganic nano/microparticles produced by chemical routes are covered by organic surfactants or polymers to control their agglomeration during their synthesis. However, these surfactants and polymers negatively affect their catalytic activity because these molecules mask the surface. This work presents the synthesis of surfactant-free CuInS2 and CuInSe2 (sf-CuInS2 and sf-CuInSe2) nano/microparticles through simple reactions without surfactant or polymer coatings using LiBH4 under a thermodynamically favourable condition. These reactions are rare observations of a single-step process to produce ternary metal chalcogenides without any template assistance. We have also demonstrated efficient catalysis by sf-CuInS2 nanoparticles in the coupling reaction of substituted phenylacetylenes. We tested it as catalysts in dimerizing 1,3-diyne derivatives while using 8-diazabicyclo[5.4.0]undec-7-ene (DBU) as the base. These Glassar–Hay coupling reactions are conducted at room temperature in acetonitrile (4–7 h, depending on the substrate) using 10 mg of sf-CuInS2. The maximum yield obtained in these reactions is 97%, while the catalyst is reusable for five cycles with little difference in its ability to catalyse. The effectiveness of the catalyst is credited to the availability of a free catalytic surface.
- 8 June 2023
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 47 (28) , 13186-13192
Dual-functional organic surfactant for the effective stabilization of nano aluminium
An innovative approach that uses the dual functional capping agent 1-aminohexanol to stabilize aluminium nanoparticles (Nano-Al) produced via the colloidal synthesis process is reported.
- 8 June 2023
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 47 (28) , 13186-13192
Dual-functional organic surfactant for the effective stabilization of nano aluminium
An innovative approach that uses the dual functional capping agent 1-aminohexanol to stabilize aluminium nanoparticles (Nano-Al) produced via the colloidal synthesis process is reported.