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Implementation of Transition Metal Phosphides as Pt-Free Catalysts for PEM Water Electrolysis
| Content Provider | MDPI |
|---|---|
| Author | Falcão, D. S. Brito, João Restivo, João Sousa, Juliana P. S. Spera, Natalia C. M. Rocha, Amadeu Pinto, A. M. F. R. Pereira, Manuel Fernando R. Soares, Olívia Salomé G. P. |
| Copyright Year | 2022 |
| Description | Proton Exchange Membrane (PEM) water electrolysis (WE) produces $H_{2}$ with a high degree of purity, requiring only water and energy. If the energy is provided from renewable energy sources, it releases “Green $H_{2}$”, a $CO_{2}$-free $H_{2}$. PEMWE uses expensive and rare noble metal catalysts, which hinder their use at a large industrial scale. In this work, the electrocatalytic properties of Transition Metal Phosphides (TMP) catalysts supported on Carbon Black (CB) for Hydrogen Evolution Reaction (HER) were investigated as an alternative to Platinum Group Metals. The physico-chemical properties and catalytic performance of the synthesized catalysts were characterized. In the ex situ experiments, the 25% FeP/CB, 50% FeP/CB and 50% CoP/CB with overpotentials of −156.0, −165.9 and −158.5 mV for a current density of 100 mA $cm^{−2}$ showed the best catalytic properties, thereby progressing to the PEMWE tests. In those tests, the 50% FeP/CB required an overpotential of 252 mV for a current density of 10 mA $cm^{−2}$, quite close to the 220 mV of the Pt catalyst. This work provides a proper approach to the synthesis and characterization of TMP supported on carbon materials for the HER, paving the way for further research in order to replace the currently used PGM in PEMWE. |
| Starting Page | 1821 |
| e-ISSN | 19961073 |
| DOI | 10.3390/en15051821 |
| Journal | Energies |
| Issue Number | 5 |
| Volume Number | 15 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2022-03-01 |
| Access Restriction | Open |
| Subject Keyword | Energies Electrochemistry Hydrogen Water Electrolysis Transition Metal Phosphides Pem |
| Content Type | Text |
| Resource Type | Article |
