TY - JOUR
T1 - Effect of Cu doping on the anatase-to-rutile phase transition in TiO2 photocatalysts
T2 - Theory and experiments
AU - Byrne, Ciara
AU - Moran, Lorraine
AU - Hermosilla, Daphne
AU - Merayo, Noemí
AU - Blanco, Ángeles
AU - Rhatigan, Stephen
AU - Hinder, Steven
AU - Ganguly, Priyanka
AU - Nolan, Michael
AU - Pillai, Suresh C.
N1 - Funding Information:
SR and MN acknowledge support from Science Foundation Ireland (SFI) through the US-Ireland R&D Partnership Program, grant number SFI 14/US/E2915 , the ERA.Net for Materials Research and Innovation (M-ERA.Net 2), Horizon 2020 grant agreement number 685451 , SFI Grant Number SFI/16/M-ERA/3418 (RATOCAT) and the European Commission through the COST Action CM1104 “Reducible Metal Oxides, Structure and Function”. We acknowledge access to computing resources at Tyndall provided by SFI and by the SFI and Higher Education Authority funded Irish Centre for High End Computing. CB, LM and SP would like to acknowledge access to Raman Spectroscopy at Centre for Research in Engineering Surface Technology (CREST), FOCAS Institute, Dublin Institute of Technology, Kevin Street. CB & PG would like to acknowledge the Institute of Technology Sligo President’s Bursary for providing financial support. SP is grateful to the Renewable Engine project funded by European Union’s INTERREG VA Programme, managed by the Special EU Programmes Body (SEUPB), with match funding provided by the Department for the Economy and Department of Jobs, Enterprise and Innovation in Ireland. DH would like to acknowledgment the Universidad de Valladolid for granting the stay at the Institute of Technology Sligo. DH would also to thank Ministerio de Economía y Competitividad of Spain (research grant number: CTM2016-77948-R ) for providing research funding.
Publisher Copyright:
© 2019
PY - 2019/6/5
Y1 - 2019/6/5
N2 - This paper shows that incorporation of Cu inhibits the anatase to rutile phase transition at temperatures above 500 °C. The control sample, with 0% Cu contained 34.3% anatase at 600 °C and transitioned to 100% rutile by 650 °C. All copper doped samples maintained 100% anatase up to 600 °C. With 2% Cu doping, anatase fully transformed to rutile at 650 °C, at higher Cu contents of 4% & 8% mixed phased samples, with 27.3% anatase and 74.3% anatase respectively, are present at 650 °C. All samples had fully transformed to rutile by 700 °C. 0%, 4% and 8% Cu were evaluated for photocatalytic degradation of 1, 4 dioxane. Without any catalyst, 15.8% of the 1,4 dioxane degraded upon irradiation with light for 4 h. Cu doped TiO2 shows poor photocatalytic degradation ability compared to the control samples. Density functional theory (DFT) studies of Cu-doped rutile and anatase show formation of charge compensating oxygen vacancies and a Cu2+ oxidation state. Reduction of Cu2+ to Cu+ and Ti4+ to Ti3+ was detected by XPS after being calcined to 650–700 °C. This reduction was also shown in DFT studies. Cu 3d states are present in the valence to conduction band energy gap upon doping. We suggest that the poor photocatalytic activity of Cu-doped TiO2, despite the high anatase content, arises from the charge recombination at defect sites that result from incorporation of copper into TiO2.
AB - This paper shows that incorporation of Cu inhibits the anatase to rutile phase transition at temperatures above 500 °C. The control sample, with 0% Cu contained 34.3% anatase at 600 °C and transitioned to 100% rutile by 650 °C. All copper doped samples maintained 100% anatase up to 600 °C. With 2% Cu doping, anatase fully transformed to rutile at 650 °C, at higher Cu contents of 4% & 8% mixed phased samples, with 27.3% anatase and 74.3% anatase respectively, are present at 650 °C. All samples had fully transformed to rutile by 700 °C. 0%, 4% and 8% Cu were evaluated for photocatalytic degradation of 1, 4 dioxane. Without any catalyst, 15.8% of the 1,4 dioxane degraded upon irradiation with light for 4 h. Cu doped TiO2 shows poor photocatalytic degradation ability compared to the control samples. Density functional theory (DFT) studies of Cu-doped rutile and anatase show formation of charge compensating oxygen vacancies and a Cu2+ oxidation state. Reduction of Cu2+ to Cu+ and Ti4+ to Ti3+ was detected by XPS after being calcined to 650–700 °C. This reduction was also shown in DFT studies. Cu 3d states are present in the valence to conduction band energy gap upon doping. We suggest that the poor photocatalytic activity of Cu-doped TiO2, despite the high anatase content, arises from the charge recombination at defect sites that result from incorporation of copper into TiO2.
KW - DFT
KW - Doping
KW - Oxygen vacancy
KW - Photocatalysis
KW - TiO
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U2 - 10.1016/j.apcatb.2019.01.058
DO - 10.1016/j.apcatb.2019.01.058
M3 - Article
AN - SCOPUS:85060736428
SN - 0926-3373
VL - 246
SP - 266
EP - 276
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -