Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles

Anatase TiO 2 nanoparticles (NPs) have the potential to photocatalyse water splitting using UV light, to thus provide hydrogen fuel in a clean and sustainable manner. Such NPs have optical gaps covering a small range of relatively high energy solar photons, giving rise to low photo-efficiencies. Alt...

Full description

Bibliographic Details
Authors: Morales García, Ángel; Macià Escatllar, Antoni; Illas i Riera, Francesc; Bromley, Stefan Thomas
Format: Article
Status:Accepted version
Publication date:2019
Country:España
Institution:Universidad de Barcelona
Repository:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/165146
Online Access:https://hdl.handle.net/2445/165146
Access Level:Open access
Keyword:Fotocatàlisi
Diòxid de titani
Nanopartícules
Photocatalysis
Titanium dioxide
Nanoparticles
_version_ 1878739628882657280
author Morales García, Ángel
author2 Macià Escatllar, Antoni
Illas i Riera, Francesc
Bromley, Stefan Thomas
author2_role author
author
author
author_browse Bromley, Stefan Thomas
Illas i Riera, Francesc
Macià Escatllar, Antoni
Morales García, Ángel
author_facet Morales García, Ángel
Macià Escatllar, Antoni
Illas i Riera, Francesc
Bromley, Stefan Thomas
author_role author
collection Dipòsit Digital de la UB
description Anatase TiO 2 nanoparticles (NPs) have the potential to photocatalyse water splitting using UV light, to thus provide hydrogen fuel in a clean and sustainable manner. Such NPs have optical gaps covering a small range of relatively high energy solar photons, giving rise to low photo-efficiencies. Although anatase NPs with 10-20 nm diameters thermodynamically prefer crystalline faceted morphologies, application of physico-chemical procedures can produce more rounded NPs with amorphous shells. Such engineered metastable core-shell NPs (so-called black TiO 2 NPs) have reduced band gaps due to shell-induced band edge broadening, resulting in higher photoactivities. For <5 nm diameters, TiO 2 NPs typically exhibit spherical-like NP morphologies, which also display enhanced photoactivity. For smaller NPs it is difficult to experimentally determine their thermodynamic stability and internal atomic structure, to help rationalise their higher photoactivities. Employing accurate electronic structure calculations, we establish the relative stability of spherical and faceted stoichiometric TiO 2 NPs with 1-3.4 nm diameters. Mirroring experimental preparation, simulated thermal annealing is found to significantly stabilise relaxed spherical cut anatase NPs. We find that the smallest spherical NPs become amorphized by annealing, but, for diameters >2 nm, annealing yields NPs with anatase-cores and amorphous-shells. Like larger black TiO 2 core-shell NPs, we confirm that our core-shell NPs are metastable relative to faceted anatase NPs and have significantly smaller optical gaps than faceted NPs. Our calculated gaps are in excellent agreement with experimental data, strongly supporting the validity of our NP models. Energy gap narrowing in these core-shell NPs is found to be due to broadening of valence band states induced by the amorphous shell, analogous to the mechanism proposed for black TiO 2 NPs. Our stoichiometric NPs also show that this band narrowing effect does not require the disordered shells to be non-stoichiometric or for incorporation of other atom types. Instead, we find that this effect mainly arises from 4-coordinated Ti atoms in the amorphous shell. Our careful and systematic computational investigation, using NP models of unprecedented realism, thus provides direct confirmation that the enhanced photoactivity in small spherical TiO 2 NP observed in experiment is due to the formation of metastable core-shell NPs with 4-coordinated Ti centres
eu_rights_str_mv openAccess
format article
id ES_c516a69063ca3e5aae7d5af33b3bf8a7
institution Universidad de Barcelona
instname_str Universidad de Barcelona
network_acronym_str ES
network_name_str España
oai_identifier_str oai:diposit.ub.edu:2445/165146
publishDate 2019
publishDateSort 2019
publisher Royal Society of Chemistry
publisherStr Royal Society of Chemistry
reponame_str Dipòsit Digital de la UB
spelling Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles Morales García, Ángel Macià Escatllar, Antoni Illas i Riera, Francesc Bromley, Stefan Thomas Fotocatàlisi Diòxid de titani Nanopartícules Photocatalysis Titanium dioxide Nanoparticles Anatase TiO 2 nanoparticles (NPs) have the potential to photocatalyse water splitting using UV light, to thus provide hydrogen fuel in a clean and sustainable manner. Such NPs have optical gaps covering a small range of relatively high energy solar photons, giving rise to low photo-efficiencies. Although anatase NPs with 10-20 nm diameters thermodynamically prefer crystalline faceted morphologies, application of physico-chemical procedures can produce more rounded NPs with amorphous shells. Such engineered metastable core-shell NPs (so-called black TiO 2 NPs) have reduced band gaps due to shell-induced band edge broadening, resulting in higher photoactivities. For <5 nm diameters, TiO 2 NPs typically exhibit spherical-like NP morphologies, which also display enhanced photoactivity. For smaller NPs it is difficult to experimentally determine their thermodynamic stability and internal atomic structure, to help rationalise their higher photoactivities. Employing accurate electronic structure calculations, we establish the relative stability of spherical and faceted stoichiometric TiO 2 NPs with 1-3.4 nm diameters. Mirroring experimental preparation, simulated thermal annealing is found to significantly stabilise relaxed spherical cut anatase NPs. We find that the smallest spherical NPs become amorphized by annealing, but, for diameters >2 nm, annealing yields NPs with anatase-cores and amorphous-shells. Like larger black TiO 2 core-shell NPs, we confirm that our core-shell NPs are metastable relative to faceted anatase NPs and have significantly smaller optical gaps than faceted NPs. Our calculated gaps are in excellent agreement with experimental data, strongly supporting the validity of our NP models. Energy gap narrowing in these core-shell NPs is found to be due to broadening of valence band states induced by the amorphous shell, analogous to the mechanism proposed for black TiO 2 NPs. Our stoichiometric NPs also show that this band narrowing effect does not require the disordered shells to be non-stoichiometric or for incorporation of other atom types. Instead, we find that this effect mainly arises from 4-coordinated Ti atoms in the amorphous shell. Our careful and systematic computational investigation, using NP models of unprecedented realism, thus provides direct confirmation that the enhanced photoactivity in small spherical TiO 2 NP observed in experiment is due to the formation of metastable core-shell NPs with 4-coordinated Ti centres Royal Society of Chemistry https://hdl.handle.net/2445/165146
spellingShingle Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
Morales García, Ángel
Fotocatàlisi
Diòxid de titani
Nanopartícules
Photocatalysis
Titanium dioxide
Nanoparticles
status_str acceptedVersion
title Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
title_full Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
title_fullStr Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
title_full_unstemmed Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
title_short Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
title_sort Understanding the interplay between size, morphology and energy gap in photoactive TiO2 nanoparticles
topic Fotocatàlisi
Diòxid de titani
Nanopartícules
Photocatalysis
Titanium dioxide
Nanoparticles
topic_facet Fotocatàlisi
Diòxid de titani
Nanopartícules
Photocatalysis
Titanium dioxide
Nanoparticles
url https://hdl.handle.net/2445/165146