Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media

Low-loading of oxidized platinum nanoparticles (0.1–0.5 wt%) was incorporated into mesoporous titanium dioxide support (Ptx/meso-TiO2) via evaporation self-assembly (ESA) approach followed by a two-step calcination processes. The physicochemical characterizations showed that the oxidized Ptx/meso-Ti...

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Main Authors: Mabrook S. Amer, Mohamed A. Ghanem, Abdullah M. Al-Mayouf, Prabhakarn Arunachalam, Nezar H. Khdary
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Arabian Journal of Chemistry
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535218300911
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spelling doaj-57c527192d7449da99cf6ddbf57a33682020-11-25T02:21:36ZengElsevierArabian Journal of Chemistry1878-53522020-01-0113122572270Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic mediaMabrook S. Amer0Mohamed A. Ghanem1Abdullah M. Al-Mayouf2Prabhakarn Arunachalam3Nezar H. Khdary4Electrochemistry Research Group, Chemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaElectrochemistry Research Group, Chemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia; Corresponding author.Electrochemistry Research Group, Chemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaElectrochemistry Research Group, Chemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi ArabiaKing Abdulaziz City for Science and Technology, Riyadh 11442, Saudi ArabiaLow-loading of oxidized platinum nanoparticles (0.1–0.5 wt%) was incorporated into mesoporous titanium dioxide support (Ptx/meso-TiO2) via evaporation self-assembly (ESA) approach followed by a two-step calcination processes. The physicochemical characterizations showed that the oxidized Ptx/meso-TiO2 catalysts exhibit high surface area around 200 m2/g and Pt nanoparticles having an average size of 3.0 nm are uniformly incorporated into the mesoporous TiO2 matrix with the existence of Pt(II) and Pt(IV) oxidation states. The Ptx/meso-TiO2 electrocatalysts showed an enhanced electrocatalytic activity with hydrogen evolution onset potential at −10 mV vs. RHE, Tafel slope of −110 mV/dec, small charge transfer resistance, and mass activity that reaches up to 25.7 A/mgPt at −300 mV vs. RHE. The hydrogen evolution mass activity of Ptx/meso-TiO2 electrocatalysts is significantly more efficient than the commercial Pt/C catalysts and Pt nanoparticles supported on nanostructured carbon substrates. Moreover, the Ptx/meso-TiO2 electrocatalysts exhibit excellent durability for a 24-hour electrolysis in acid solution with a further current activation during the prolonged electrolysis. The enhanced mass activity and durability are attributed to the substrate mesoporosity, uniform distribution and strong bonding between the oxidized Pt nanoparticles and the TiO2 substrate. These results demonstrate the promise of the mesoporous TiO2 substrate modified with low loading of platinum nanoparticles for energy conversion technologies. Keywords: Oxidized Pt nanoparticles, Mesoporous TiO2, Electrocatalyst, Hydrogen evolutionhttp://www.sciencedirect.com/science/article/pii/S1878535218300911
collection DOAJ
language English
format Article
sources DOAJ
author Mabrook S. Amer
Mohamed A. Ghanem
Abdullah M. Al-Mayouf
Prabhakarn Arunachalam
Nezar H. Khdary
spellingShingle Mabrook S. Amer
Mohamed A. Ghanem
Abdullah M. Al-Mayouf
Prabhakarn Arunachalam
Nezar H. Khdary
Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
Arabian Journal of Chemistry
author_facet Mabrook S. Amer
Mohamed A. Ghanem
Abdullah M. Al-Mayouf
Prabhakarn Arunachalam
Nezar H. Khdary
author_sort Mabrook S. Amer
title Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
title_short Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
title_full Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
title_fullStr Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
title_full_unstemmed Low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
title_sort low-loading of oxidized platinum nanoparticles into mesoporous titanium dioxide for effective and durable hydrogen evolution in acidic media
publisher Elsevier
series Arabian Journal of Chemistry
issn 1878-5352
publishDate 2020-01-01
description Low-loading of oxidized platinum nanoparticles (0.1–0.5 wt%) was incorporated into mesoporous titanium dioxide support (Ptx/meso-TiO2) via evaporation self-assembly (ESA) approach followed by a two-step calcination processes. The physicochemical characterizations showed that the oxidized Ptx/meso-TiO2 catalysts exhibit high surface area around 200 m2/g and Pt nanoparticles having an average size of 3.0 nm are uniformly incorporated into the mesoporous TiO2 matrix with the existence of Pt(II) and Pt(IV) oxidation states. The Ptx/meso-TiO2 electrocatalysts showed an enhanced electrocatalytic activity with hydrogen evolution onset potential at −10 mV vs. RHE, Tafel slope of −110 mV/dec, small charge transfer resistance, and mass activity that reaches up to 25.7 A/mgPt at −300 mV vs. RHE. The hydrogen evolution mass activity of Ptx/meso-TiO2 electrocatalysts is significantly more efficient than the commercial Pt/C catalysts and Pt nanoparticles supported on nanostructured carbon substrates. Moreover, the Ptx/meso-TiO2 electrocatalysts exhibit excellent durability for a 24-hour electrolysis in acid solution with a further current activation during the prolonged electrolysis. The enhanced mass activity and durability are attributed to the substrate mesoporosity, uniform distribution and strong bonding between the oxidized Pt nanoparticles and the TiO2 substrate. These results demonstrate the promise of the mesoporous TiO2 substrate modified with low loading of platinum nanoparticles for energy conversion technologies. Keywords: Oxidized Pt nanoparticles, Mesoporous TiO2, Electrocatalyst, Hydrogen evolution
url http://www.sciencedirect.com/science/article/pii/S1878535218300911
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