Jorge Montero
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Jorge Montero has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
- Alessandra D’ Epifanio
Department of Chemical Science and Technologies, University of Rome Tor Vergata, Via Della Ricerca Scientifica 1, 00133 Rome, Italy
5 shared publications - Barbara Mecheri
Department of Chemical Science and Technologies, University of Rome Tor Vergata, Via Della Ricerca Scientifica 1, 00133 Rome, Italy
5 shared publications - Silvia Licoccia
NAST Centre, University of Rome Tor Vergata, 00133 Rome, Italy
3 shared publications - Khair Un Nisa
Department of Chemical Science and Technologies, University of Rome Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy
2 shared publications - Mattia Forchetta
Department of Chemical Science and Technologies University of Rome Tor Vergata Via della Ricerca Scientifica 00133 Rome Italy
2 shared publications - Pierluca Galloni
Department of Chemical Science and Technologies, University of Rome Tor Vergata, via della Ricerca Scientifica snc, Rome 00133, Italy
2 shared publications
Latest Publications
- 26 September 2026
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 278
Ceria-based co-catalysts, supported on reduced graphene oxide, for the oxygen reduction in PEM fuel cells
- 26 September 2026
- Published by Elsevier in International Journal of Hydrogen Energy
- Vol. 278
Ceria-based co-catalysts, supported on reduced graphene oxide, for the oxygen reduction in PEM fuel cells
- Open Access
Hierarchical porous Fe/Ni-based bifunctional oxygen electrocatalysts for rechargeable zinc-air batteries
- Open Access
Development and Optimization of Air-Electrodes for Rechargeable Zn–Air Batteries
Rechargeable Zn–air batteries (ZABs) can play a significant role in the transition to a cleaner and more sustainable energy system due to their high theoretical energy density, high cell voltage, and environmental friendliness. ZAB’s air cathode is the principal determinant in predicting the battery’s overall performance, as it is responsible for catalyzing the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) during the discharging and charging process, respectively. In this work, a detailed optimization study of the architecture of the air cathode was carried out using the benchmark bifunctional oxygen electrocatalyst (Pt/C-RuO2). The air cathode composition and architecture were optimized regarding the choice of the commercial gas diffusion layer (GDL), the effect of hot pressing the catalyst layer (CL), and the optimum pore size of the current collector. The best cathode from this study shows a maximum power density (PDmax) of 167 mW/cm2, with a round trip efficiency and a voltage gap (Egap) of 59.8% and 0.78 V, respectively, indicating the air cathodes preparation approach proposed in this work as a promising strategy for the improvement of the overall performance of ZABs.
Open AccessDevelopment and Optimization of Air-Electrodes for Rechargeable Zn–Air Batteries
Rechargeable Zn–air batteries (ZABs) can play a significant role in the transition to a cleaner and more sustainable energy system due to their high theoretical energy density, high cell voltage, and environmental friendliness. ZAB’s air cathode is the principal determinant in predicting the battery’s overall performance, as it is responsible for catalyzing the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) during the discharging and charging process, respectively. In this work, a detailed optimization study of the architecture of the air cathode was carried out using the benchmark bifunctional oxygen electrocatalyst (Pt/C-RuO2). The air cathode composition and architecture were optimized regarding the choice of the commercial gas diffusion layer (GDL), the effect of hot pressing the catalyst layer (CL), and the optimum pore size of the current collector. The best cathode from this study shows a maximum power density (PDmax) of 167 mW/cm2, with a round trip efficiency and a voltage gap (Egap) of 59.8% and 0.78 V, respectively, indicating the air cathodes preparation approach proposed in this work as a promising strategy for the improvement of the overall performance of ZABs.
- 21 December 2022
- Published by Wiley in ChemElectroChem
- Vol. 10 (2)
Cover Feature: A Neutral‐pH Aqueous Redox Flow Battery Based on Sustainable Organic Electrolytes (ChemElectroChem 2/2023)
- 21 December 2022
- Published by Wiley in ChemElectroChem
- Vol. 10 (2)
Cover Feature: A Neutral‐pH Aqueous Redox Flow Battery Based on Sustainable Organic Electrolytes (ChemElectroChem 2/2023)
- Open Access
- 13 December 2022
- Published by Wiley in ChemElectroChem
- Vol. 10 (2)
A Neutral‐pH Aqueous Redox Flow Battery Based on Sustainable Organic Electrolytes
Aqueous organic redox flow batteries (AORFBs) have gained increasing attention for large‐scale storage due to the advantages of decoupled energy and power, safe and sustainable chemistry, and tunability of the redox‐active species. Here, we report the development of a neutral‐pH AORFB assembled with a highly water‐soluble ferrocene 1,1‐disulfonic disodium salt (DS−Fc) and two viologen derivatives, 1,1’‐bis(3‐sulfonatopropyl)‐viologen (BSP−Vi) and Bis(3‐trimethylammonium)propyl viologen tetrachloride (BTMAP−Vi). Synthesized electrolytes showed excellent redox potential, good diffusion coefficient, and a good transfer rate constant. In particular, BSP−Vi has a more negative redox potential (‐0.4 V) than BTMAP−Vi (−0.3 V) and faster kinetics; therefore, it was selected to be assembled in an AORFB as anolyte, coupled with DS−Fc as catholyte.The resulting AORFB based on BTMAP−Vi/DS−Fc and BSP−Vi/DS−Fc redox couple had a high cell voltage (1.2 V and 1.3 V, respectively) and theoretical energy density (13 WhL−1 and 14 WhL−1 respectively) and was able to sustain 70 charge‐discharge cycles with energy efficiency as high as 97 %.
- 13 December 2022
- Published by Wiley in ChemElectroChem
- Vol. 10 (2)
Open AccessA Neutral‐pH Aqueous Redox Flow Battery Based on Sustainable Organic Electrolytes
Aqueous organic redox flow batteries (AORFBs) have gained increasing attention for large‐scale storage due to the advantages of decoupled energy and power, safe and sustainable chemistry, and tunability of the redox‐active species. Here, we report the development of a neutral‐pH AORFB assembled with a highly water‐soluble ferrocene 1,1‐disulfonic disodium salt (DS−Fc) and two viologen derivatives, 1,1’‐bis(3‐sulfonatopropyl)‐viologen (BSP−Vi) and Bis(3‐trimethylammonium)propyl viologen tetrachloride (BTMAP−Vi). Synthesized electrolytes showed excellent redox potential, good diffusion coefficient, and a good transfer rate constant. In particular, BSP−Vi has a more negative redox potential (‐0.4 V) than BTMAP−Vi (−0.3 V) and faster kinetics; therefore, it was selected to be assembled in an AORFB as anolyte, coupled with DS−Fc as catholyte.The resulting AORFB based on BTMAP−Vi/DS−Fc and BSP−Vi/DS−Fc redox couple had a high cell voltage (1.2 V and 1.3 V, respectively) and theoretical energy density (13 WhL−1 and 14 WhL−1 respectively) and was able to sustain 70 charge‐discharge cycles with energy efficiency as high as 97 %.
- Open Access
- 1 August 2021
- Published by Elsevier in Journal of Electroanalytical Chemistry
- Vol. 895
Redox-active coordination polymers as bifunctional electrolytes in slurry-based aqueous batteries at neutral pH
- 1 August 2021
- Published by Elsevier in Journal of Electroanalytical Chemistry
- Vol. 895
Open AccessRedox-active coordination polymers as bifunctional electrolytes in slurry-based aqueous batteries at neutral pH