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Phosphate stabilized PdCoP@Nifoam catalyst for self-pressurized H2 production from the electrochemical reforming of ethanol at 150 °C

Authors :
Alessandro Lavacchi
Maria V. Pagliaro
Francesco Vizza
Hamish A. Miller
Carlo Bartoli
Marco Bellini
Source :
Journal of catalysis (Online) 382 (2020): 237–246. doi:10.1016/j.jcat.2019.12.019, info:cnr-pdr/source/autori:Maria Vincenza Pagliaro, Marco Bellini, Alessandro Lavacchi, Hamish Andrew Miller, Carlo Bartoli, Francesco Vizza/titolo:Phosphate stabilized PdCoP@Nifoam catalyst for self-pressurized H2 production from the electrochemical reforming of ethanol at 150 °C/doi:10.1016%2Fj.jcat.2019.12.019/rivista:Journal of catalysis (Online)/anno:2020/pagina_da:237/pagina_a:246/intervallo_pagine:237–246/volume:382
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

The electrochemical reforming of ethanol to H2 is achieved at 150 °C in an autoclave electrochemical cell that allows the safe pressurization of the H2 produced as no O2 is evolved. The alkaline conditions are very aggressive to catalysts including noble metals like Pt and Pd. We report a highly active ethanol oxidation catalyst (PdCoNifoam) composed of Pd nanoparticles supported on nanostructured Co oxide structures grown on nickel foam. Treatment with phosphorous vapors at high temperature yields a thin coating of phosphate that confers enhanced stability to the electrode operating in an electrolysis cell at 150 °C. A combination of scanning electron microscopy (energy dispersive X-ray spectroscopy) and X-ray photoelectron spectroscopy reveal a 3D nano-flake surface with an external layer of phosphates that prevents Pd dissolution. The PdCoP@Nifoam catalyst was successfully used for ethanol electrochemical reforming at 150 °C with self-pressurization of the H2 produced by the electrochemical reaction.

Details

ISSN :
00219517
Volume :
382
Database :
OpenAIRE
Journal :
Journal of Catalysis
Accession number :
edsair.doi.dedup.....772c0d8691b126ef35a9b8cab8176a87
Full Text :
https://doi.org/10.1016/j.jcat.2019.12.019