CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Synthesis of High Surface Area TiO2 Aerogel Support with Pt Nanoparticle Catalyst and CO Oxidation Study
Authors
Chan Ho Jung
Hanseul Choi
+5 more
Jeong Young Park
Matthias M. Koebel
Michele Carboni
Song Yi Moon
You Kyung Kim
Publication date
1 May 2018
Publisher
'Springer Fachmedien Wiesbaden GmbH'
Abstract
We demonstrate the preparation and catalytic testing of nanocatalysts composed of TiO2 synthesized in aerogel using a supercritical drying process with Pt nanoparticles deposited on the mesopore oxide surface. By controlling the aging time, we found conditions that led to TiO2 with a surface area among the highest ever reported for a TiO2 material in aerogel form (similar to 685 m(2) g(- 1)). The chosen synthesis route also features good control over the pore volume and pore size. Even though our aerogel TiO2 support showed an amorphous structure before calcination, 90.2% anatase and 9.8% rutile phases co-existed after calcination at 500 A degrees C for 2 h with an average particle size of about 17 nm based on XRD results. The as-synthesized TiO2 and Pt/TiO2 were both used as catalysts for the CO oxidation reaction. Uncalcined Pt/TiO2 showed 100% conversion at 300 A degrees C. After calcination, Pt/TiO2 exhibited a significantly higher catalytic activity, showing 100% conversion at 125 A degrees C and an activation energy of only 13.4 kcal mol(- 1). We show that TiO2 synthesized by the aerogel method can be an excellent support material for nanocatalysis because of its high surface area and facile and scalable synthesis. © Springer Science+Business Media, LLC, part of Springer Nature 201
Similar works
Full text
Available Versions
IBS Publications Repository
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:pr.ibs.re.kr:8788114/6195
Last time updated on 06/02/2020