Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)

Hydrogen evolution reaction (HER) is the fundamental half-reaction involved in hydrogen gas production. HER is a cathodic reaction in electrolysis, where proton is converted into H2 gas with the help of a electrocatalyst. Platinum (Pt)-based catalysts are known to be the most effective catalysts for...

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Main Author: Hung, Hsi Chien
Other Authors: Liu Zheng
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2021
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Online Access:https://hdl.handle.net/10356/147790
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1477902023-03-04T15:44:57Z Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER) Hung, Hsi Chien Liu Zheng School of Materials Science and Engineering Z.Liu@ntu.edu.sg Engineering::Materials::Nanostructured materials Hydrogen evolution reaction (HER) is the fundamental half-reaction involved in hydrogen gas production. HER is a cathodic reaction in electrolysis, where proton is converted into H2 gas with the help of a electrocatalyst. Platinum (Pt)-based catalysts are known to be the most effective catalysts for HER. In this study, Graphene-Pt-SiO2 electrocatalyst is fabricated by encapsulating graphene-supported Pt nanoparticles with ultrathin mesoporous silica mesh with thicknesses ranging from 0.1 to 10 nm. AFM images showed that the aggregation issue of Pt nanoparticles is greatly suppressed by the mesoporous silica layer. Tafel slopes corresponding to HER in 0.5 M H2SO4 solution are decreased from 86 to 58 mV dec−1 when the silica thickness is reduced from 2.0nm to 0.2nm, revealing that thinner silica coatings resulted in better catalytic activities. The remarkable catalytic stability and activity can be attributed to porous network of the SiO2 layers, which not only prevented Pt from sintering during HER, but also allowed reactant molecules to be transported through its pores easily to reach the active catalytic sites on encapsulated Pt nanoparticles. Importantly, 0.2nm and 0.6nm SiO2-encapsulated electrocatalysts were found to have the best HER activities, with a Tafel slope of 58 and 57 mV dec−1 respectively. Fundamental insights into HER reaction mechanism are discussed. The 2 main strategies commonly employed for the improvement of catalytic performance and stability based on (1) core-shell configuration and (2) encapsulation by mesoporous layer are also described in the literature review. The enhanced electrochemical properties for Pt-based nanoparticles opened doors to a more cost-efficient and stable electrocatalyst for the promotion of hydrogen economy in the future. Bachelor of Engineering (Materials Engineering) 2021-04-29T04:34:07Z 2021-04-29T04:34:07Z 2021 Final Year Project (FYP) Hung, H. C. (2021). Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER). Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/147790 https://hdl.handle.net/10356/147790 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials::Nanostructured materials
spellingShingle Engineering::Materials::Nanostructured materials
Hung, Hsi Chien
Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
description Hydrogen evolution reaction (HER) is the fundamental half-reaction involved in hydrogen gas production. HER is a cathodic reaction in electrolysis, where proton is converted into H2 gas with the help of a electrocatalyst. Platinum (Pt)-based catalysts are known to be the most effective catalysts for HER. In this study, Graphene-Pt-SiO2 electrocatalyst is fabricated by encapsulating graphene-supported Pt nanoparticles with ultrathin mesoporous silica mesh with thicknesses ranging from 0.1 to 10 nm. AFM images showed that the aggregation issue of Pt nanoparticles is greatly suppressed by the mesoporous silica layer. Tafel slopes corresponding to HER in 0.5 M H2SO4 solution are decreased from 86 to 58 mV dec−1 when the silica thickness is reduced from 2.0nm to 0.2nm, revealing that thinner silica coatings resulted in better catalytic activities. The remarkable catalytic stability and activity can be attributed to porous network of the SiO2 layers, which not only prevented Pt from sintering during HER, but also allowed reactant molecules to be transported through its pores easily to reach the active catalytic sites on encapsulated Pt nanoparticles. Importantly, 0.2nm and 0.6nm SiO2-encapsulated electrocatalysts were found to have the best HER activities, with a Tafel slope of 58 and 57 mV dec−1 respectively. Fundamental insights into HER reaction mechanism are discussed. The 2 main strategies commonly employed for the improvement of catalytic performance and stability based on (1) core-shell configuration and (2) encapsulation by mesoporous layer are also described in the literature review. The enhanced electrochemical properties for Pt-based nanoparticles opened doors to a more cost-efficient and stable electrocatalyst for the promotion of hydrogen economy in the future.
author2 Liu Zheng
author_facet Liu Zheng
Hung, Hsi Chien
format Final Year Project
author Hung, Hsi Chien
author_sort Hung, Hsi Chien
title Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
title_short Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
title_full Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
title_fullStr Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
title_full_unstemmed Ultrathin silica mesh protected Pt nanoparticles for hydrogen evolution reaction (HER)
title_sort ultrathin silica mesh protected pt nanoparticles for hydrogen evolution reaction (her)
publisher Nanyang Technological University
publishDate 2021
url https://hdl.handle.net/10356/147790
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