Tushar A. Kharde
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Tushar A. Kharde has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Sanjay Kumar Singh
Catalysis Group, Department of Chemistry, Indian Institute of Technology Indore, Khandwa Road, Simrol, Indore 453552, Madhya Pradesh, India
3 shared publications Abhijit Shrotri
1 shared publicationAnkit Kumar
1 shared publication- Ankit Kumar
Catalysis Group, Department of Chemistry, Indian Institute of Technology Indore, Khandwa Road, Simrol, Indore, 453552, M.P., India
1 shared publication Bhanu Priya
1 shared publication- Jayashree Parthiban
Catalysis Group Department of Chemistry Indian Institute of Technology Indore Indore Madhya Pradesh India
1 shared publication
Latest Publications
- Open Access
- 5 October 2026
- Published by Royal Society of Chemistry (RSC) in Materials Advances
- Vol. 7 (19) , 9611-9619
Selective production of CO 2 -free hydrogen gas and formate from ethylene glycol over supported Ru catalysts
Ru nanoparticles on La(OH) 3 enable low-temperature (130 °C) selective reforming of aqueous ethylene glycol with high yield of CO 2 -free H 2 and formate, and the process can be coupled with one-pot PET depolymerization for hydrogen production.
- 5 October 2026
- Published by Royal Society of Chemistry (RSC) in Materials Advances
- Vol. 7 (19) , 9611-9619
Open AccessSelective production of CO 2 -free hydrogen gas and formate from ethylene glycol over supported Ru catalysts
Ru nanoparticles on La(OH) 3 enable low-temperature (130 °C) selective reforming of aqueous ethylene glycol with high yield of CO 2 -free H 2 and formate, and the process can be coupled with one-pot PET depolymerization for hydrogen production.
- 30 January 2024
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 53 (10) , 4363-4389
Recent progress in molecular transition metal catalysts for hydrogen production from methanol and formaldehyde
Hydrogen is considered as a potential alternative and sustainable energy carrier, but its safe storage and transportation are still challenging due to its low volumetric energy density. Notably, C1-based substrates, methanol and formaldehyde, containing high hydrogen contents of 12.5 wt% and 6.7 wt%, respectively, can release hydrogen on demand in the presence of a suitable catalyst. Advantageously, both methanol and aqueous formaldehyde are liquid at room temperature, and hence can be stored and transported considerably more safely than hydrogen gas. Moreover, these C1-based substrates can be produced from biomass waste and can also be regenerated from CO2, a greenhouse gas. In this review, the recent progress in hydrogen production from methanol and formaldehyde over noble to non-noble metal complex-based molecular transition metal catalysts is extensively reviewed. This review also focuses on the critical role of the structure–activity relationship of the catalyst in the dehydrogenation pathway.
- 30 January 2024
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 53 (10) , 4363-4389
Recent progress in molecular transition metal catalysts for hydrogen production from methanol and formaldehyde
Hydrogen is considered as a potential alternative and sustainable energy carrier, but its safe storage and transportation are still challenging due to its low volumetric energy density. Notably, C1-based substrates, methanol and formaldehyde, containing high hydrogen contents of 12.5 wt% and 6.7 wt%, respectively, can release hydrogen on demand in the presence of a suitable catalyst. Advantageously, both methanol and aqueous formaldehyde are liquid at room temperature, and hence can be stored and transported considerably more safely than hydrogen gas. Moreover, these C1-based substrates can be produced from biomass waste and can also be regenerated from CO2, a greenhouse gas. In this review, the recent progress in hydrogen production from methanol and formaldehyde over noble to non-noble metal complex-based molecular transition metal catalysts is extensively reviewed. This review also focuses on the critical role of the structure–activity relationship of the catalyst in the dehydrogenation pathway.