HYBRID EVENT: You can participate in person at Rome, Italy or Virtually from your home or work.

10th Edition of World Nanotechnology Conference

March 10-12, 2025

March 10 -12, 2025 | Rome, Italy
World Nano 2022

Diogo M F Santos

Diogo M F Santos, Speaker at Nanotechnology conferences
Instituto Superior Técnico, ULisboa, Portugal
Title : Pt-M (M=Ni,Fe,Cu) alloys supported on graphene nanoplatelets as bifunctional electrocatalysts for ORR/OER


Alkaline water electrolysis is a well-established technology for hydrogen production. If the required electricity comes from renewable energy sources (e.g., solar, wind), green hydrogen will be generated. Improving hydrogen (HER) and oxygen evolution reaction (OER) efficiency is essential to make electrolysis more competitive with dominant fossil fuel-based technologies. That requires developing efficient electrocatalytic materials for fuel and oxygen electrodes. In this study, PtM (M=Ni,Fe,Cu) alloy nanoparticles were supported on graphene nanoplatelets (GNPs) and tested as bifunctional electrocatalysts for the oxygen evolution (OER) and oxygen reduction (ORR) reactions. Bifunctional electrocatalysts can be applied in unitized regenerative fuel cells (URFCs), as these devices work in two operation modes: electrolysis mode, converting water to hydrogen and oxygen when there is a surplus of electricity, and fuel cell mode, in which hydrogen and oxygen are consumed when there is a need for extra power. The PtM/GNPs were synthesized via simultaneous supercritical carbon dioxide (scCO2) deposition technique, where the primary metal (Pt) and secondary metal (Ni, Fe, Cu) were deposited onto GNPs by scCO2 in the same step. This resulted in ca. 20 wt.% Pt loading and M loading in the 1.4 - 3.4 wt.% range. Morphology analysis by TEM revealed the formation of metal nanoparticles of 2–3 nm size uniformly distributed over GNPs, while XPS was used to determine their oxidation states. The electrocatalytic activity of the produced materials towards ORR was investigated in 0.1 M KOH by performing a series of linear scan voltammetry experiments at different rotation rates. The data allowed calculating the number of exchanged electrons, n, and the Tafel slope, b, two critical parameters for electrocatalysts’ evaluation. PtFe/GNPs exhibited favorable ORR kinetics in terms of the highest diffusion-limited current density, low Tafel slope, and high number of exchanged electrons (n = 3.66), which might be attributed to its high double-layer capacitance and, thus, high electrochemically active surface area. Furthermore, this material performance was comparable to that of commercial Pt/C electrocatalyst containing double the amount of Pt. PtFe/GNPs also showed the best performance toward OER as evidenced by the high current density, the lowest overpotential to reach a current density of 10 mA cm-2, and the lowest Tafel slope. The results show a great potential of the synthesized PtFe/GNPs as bifunctional catalysts for OER/ORR in URFCs.

Audience take-away:

  • This presentation will present the fundamentals of green hydrogen production by alkaline water electrolysis.
  • Then, a particular study on the development of bifunctional catalysts for OER/ORR will show the possibility of incorporating such catalysts in the oxygen electrode of URFCs for enhancing the efficiency of green hydrogen production (electrolysis mode) and simultaneously boosting the oxygen reduction reaction kinetics (fuel cell mode).


Diogo M.F. Santos is an Invited Assistant Professor at Instituto Superior Técnico (ULisboa, Portugal) and Researcher in the Center of Physics and Engineering of Advanced Materials, studying electrodes and membranes for application in direct liquid fuel cells. D.M.F. Santos has authored 120 journal papers and 90 conference proceedings, and his current h index is 30. He is in the “World’s Top 2% Scientists list” of Stanford University for the impact in 2020. D.M.F. Santos has presented more than 60 oral communications and 80 posters at international conferences. His main research interests are related to electrochemical energy conversion and storage.