Research Work at a Glance
Nanoscience and nanotechnology for energy conversion and storage
Nanoscience and nanotechnology for energy conversion and storage
Electrocatalytic water/seawater splitting research (nanostructured catalysts)
Green Hydrogen (H₂) production, with its high calorific value and potential for net-zero carbon emissions in fuel cell engines, is a highly sought-after area of research and commercial development worldwide. Electrocatalytic water splitting in an electrolyzer stands out as one of the most promising approaches for H₂ production. Advanced research has revealed various mechanisms for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) on electrocatalyst surfaces to enhance water splitting efficiency. Literature suggests that moderate adsorption free energy (ΔG(H*) ≈ 0) and high surface coverage by H* (the active species or adsorbed hydrogen) are key for HER. Similarly, for effective OER, moderate adsorption/desorption free energy, high surface coverage by *O, *OH, and *OOH active species, and the lowest energy barriers are essential. By optimizing electrocatalysts based on these factors, it is possible to enhance the efficiency of multiple electron-coupled transfer half-cell reactions and the overall electrocatalytic water splitting process (ΔGo = +237.2 kJ/mol, ΔE = 1.23 V). This optimization can reduce overpotentials, while improving stability, mass activity, and exchange current density.
Keeping these points in mind, our group developed a few novel and interesting nanostructured electrocatalysts suitable for efficient alkaline seawater/natural water splitting reaction to produce green hydrogen. By Sasanka Deka
Torus-shaped Mo0.1Ni1.9P nanoparticles having hollow nanorings at the center is synthesized using a single-step one-pot colloidal synthesis method. The nanoring particles act as highly efficient standalone electrocatalysts for alkaline water and seawater splitting at low cell voltage with high turnover frequency. This novel catalyst offers high stability under industrial harsh conditions.
Small, 2024, ASAP 2408036
Electrocatalysis🫱
ACS Catal. 2023, 13, 16, 10615–10626
We have introduced a highly effective, eco-friendly, and cost-efficient strategy for significantly enhancing photocatalytic green H2 and H2O2 production using an in-situ synthesized Pd single-atom catalyst (SAC) on indirect band gap CuCo2S4 semiconductor surface. Our findings reveal that anchoring Pd SAs enhances charge carrier migration and modifies the charge density distribution on the catalyst surface under visible light irradiation
Adv. Funct. Mater. 2025, 2507783
ACS Applied Energy Materials 2022 5 (9), 11113-11121
J. Mater. Chem. A,2020,8, 13328–13339
J. Mater. Chem. A,2019,7, 6985–6994
Electrochemical supercapacitors (SCs) are a highly efficient and promising type of rechargeable energy storage system (EES) that has garnered significant attention in recent years. This is due to their rapid charging and discharging capabilities (thanks to fast redox reaction kinetics), along with high capacity, power and energy densities, and long cycle life. Compared to commercial batteries, SCs are emerging as one of the most promising EES technologies, as both electrical and chemical energy are carried by the same carrier, the electron. SCs have proven to be highly reliable in applications such as lightweight portable electronic devices and hybrid power vehicles. With the rapid advancement in the field of nanoscience and nanotechnology, the electrochemical performances of supercapacitors have been significantly improved. This is attributed to the electrode’s high surface area for storing charges and the ease with which the electrolyte diffuses into the nanostructured electrodes. However, the current obstruction in the performance of SCs is their low energy density and it still remains a bottleneck. As a contribution to this field, we have developed a few highly efficient functional nanostructured materials/electrodes to store energy electrochemically. These include nanostructured NiCo2O4, SnS2, g-C3N4, CuCoB, NiCoCuB, SnCoSe, ZnCoNi-LDH, CuCo-LDH, etc.
Among various working electrode materials explored for supercapacitors, nanostructured transition metal oxides containing mixed metals are highly specific and special, because of their stability, variable oxidation states of the constituted metal ions, possibility to tune the mixed metal combinations, and existence of new battery types and extrinsic pseudocapacitance.
Review: Dalton Trans., 2023, 52, 839
Cobalt metal-free crystalline NiCuB alloy particles with nanowire-type morphology are developed by a new synthesis process for this sustainable development. The optimized composition Ni0.6Cu0.4B is found to have the maximum synergy effect among the metals and the metalloid.
Energy Fuels 2024, 38, 21, 21510–21520
A symmetric two-electrode coin cell device of NiCuCoB in 6.0 M KOH offers 358 F/g specific capacitance with 56 Wh/kg energy and 13,320 W/kg power density, with 50,000 cycling stability.
Journal of Energy Storage 72 (2023) 108435
With the evolution of supercapacitors, flexible and wearable electronic devices acting as promising soft power sources have gained tremendous attention. Such a device with extreme bending, twisting, and foldable features and extraordinary riveting properties like high capacitance, long cycling stability and small size perhaps will be one of the best suitable patch devices in the near future. We made several flexible supercapacitor devices in the lab, which show a highly stable electrochemical performance even under extreme mechanical deformations and no leakage or evaporation of the electrolyte on bending the cell at different angles. These are made with the materials developed as mentioned above.
Dr. C.S. Gopinath, NCL-Pune
Dr. Manash R. Das (CSIR-NEIST, Jorhat)
Dr. Ankur K Guha (Cotton University, Guwahati, Assam)
Dr. Samira Siahrostami (Simon Fraser University, Canada)
Prof. S.A. Hashmi, Physics-DU
Prof. Sameer Sapra (IIT-Delhi)
Dr. Lakshi Saikia (CSIR-NEIST, Jorhat)
Dr. Akhtar Hussain (Handique Girls’ College, Guwahati)
Dr. Tanushree Bala (University of Calcutta, Kolkata)
1. “Morphology oriented nanostructured ternary metal chalcogenide semiconductors and their use of” funded by CSIR (Council of Scientific and Industrial Research), New Delhi, 2023-2026.
2. “Development of single atom catalysts (SAC) for superior and robust photocatalytic applications” funded by SERB-DST (Science and Engineering Research Board), 2022-2025.
3. “Development of nanostructured mixed metal oxide and metal chalcogenide materials based effective electrodes and their use in supercapacitor devices” funded by TMD-DST (Department of Science and Technology, India), 2019-2022.
4. “Development of advanced nanomaterials for benchmark electrocatalytic hydrogen and oxygen evolution from water” funded by SERB-DST (Science and Engineering Research Board), 2017-2020.
5. “Synthesis, characterization and advanced multifunctional applications of novel chalcogenide semiconductor nanocrystals” funded by CSIR (Council of Scientific and Industrial Research), New Delhi, 2014-2018.
6. “Synthesis, characterization and evaluation of anticancer activity of novel bioessential transition metal complexes having tumor targeting and antitumor active ligands” funded by DBT (Department of Biotechnology), 2014-2018.
7. “Synthesis, characterization, porous assembly and application of novel metal-metal oxide hybrid nanocrystals” funded by SERB-DST, 2012-2025.
8. “Studies on the optical and magnetic properties of semiconductor-magnetic oxide hybrid nanocrystals” funded by BRNS-BARC-DAE (department of Atomic Energy), 2012-2015.
9. “Synthesis and studies of the optical, plasmonic and magnetic behavior of Ni/Ag-semiconductor hybrid nanostructures” funded by DST-DAAD (German Academic Exchange Service, Indo German), 2014-2016.
10. “Complex nanostructures and their applications in optics, photonics and electronics” funded by DST Purse grant, 2011, 2015, 2016.
11. University of Delhi Institute of Excellence (IoE) minor project 2021, 2022, 2023 and 2024.
12. University of Delhi funding through Faculty rechrage program/SEED money 2010 to 2024.