Photocatalytic activity and the radiative lifetimes of excitons via an ab initio approach

This work presents the radiative lifetimes of photogenerated electron-hole (e-h) pairs in bulk anatase and rutile TiO 2 calculated by solving the Bethe-Salpeter equation (BSE) at the G 0 W 0 [F. Fuchs, J. Furthmüller, F. Bechstedt, M. Shishkin and G. Kresse, Phys. Rev. B: Condens. Matter Mater. Phys...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (31), p.1527-1532
Hauptverfasser: Hu, Linping, Xu, Chao, Peng, Liang, Gu, Feng Long, Yang, Weitao
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container_issue 31
container_start_page 1527
container_title Journal of materials chemistry. A, Materials for energy and sustainability
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creator Hu, Linping
Xu, Chao
Peng, Liang
Gu, Feng Long
Yang, Weitao
description This work presents the radiative lifetimes of photogenerated electron-hole (e-h) pairs in bulk anatase and rutile TiO 2 calculated by solving the Bethe-Salpeter equation (BSE) at the G 0 W 0 [F. Fuchs, J. Furthmüller, F. Bechstedt, M. Shishkin and G. Kresse, Phys. Rev. B: Condens. Matter Mater. Phys., 2007, 76 , 115109] level with Perdew-Burke-Ernzerhof (PBE) GGA as the starting point, an approach labeled as PBE- G 0 W 0 -BSE, where G 0 W 0 is the non-self-consistent GW approximation. The geometry optimization and the electronic ground state are determined using PBE. G 0 W 0 , considered as the "gold standard" for band structure calculations, provides band gap results of anatase and rutile in good agreement with experimental values. By solving BSE that surmounts the single-particle picture of individual quasielectron and quasihole excitation, the approach for calculating radiative lifetime shakes off the dependence on the band structure in DFT calculations and the renormalization factors in GW approximation. For anatase, the calculated intrinsic lifetime of the lowest optically active bright excitons turns out to be several microseconds, while that of rutile is a few picoseconds. Overall, the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile, showing good agreement with the experimentally measured values. Longer lifetimes of excitons in anatase lead to observed better photocatalytic activity of these two common TiO 2 phases. Our ab initio calculations of exciton lifetimes provide a new insight into understanding the correlation of the widely applicable packing factor model [X. Lin, J. Wu, X. Lue, Z. Shan, W. Wang and F. Huang, Phys. Chem. Chem. Phys., 2009, 11 , 10047-10052] with photocatalytic activity, and also a predictive and convenient tool for designing novel materials with potential applications in photonics and optoelectronics. Ab initio calculations show that the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile.
doi_str_mv 10.1039/c8ta04140g
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Fuchs, J. Furthmüller, F. Bechstedt, M. Shishkin and G. Kresse, Phys. Rev. B: Condens. Matter Mater. Phys., 2007, 76 , 115109] level with Perdew-Burke-Ernzerhof (PBE) GGA as the starting point, an approach labeled as PBE- G 0 W 0 -BSE, where G 0 W 0 is the non-self-consistent GW approximation. The geometry optimization and the electronic ground state are determined using PBE. G 0 W 0 , considered as the "gold standard" for band structure calculations, provides band gap results of anatase and rutile in good agreement with experimental values. By solving BSE that surmounts the single-particle picture of individual quasielectron and quasihole excitation, the approach for calculating radiative lifetime shakes off the dependence on the band structure in DFT calculations and the renormalization factors in GW approximation. For anatase, the calculated intrinsic lifetime of the lowest optically active bright excitons turns out to be several microseconds, while that of rutile is a few picoseconds. Overall, the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile, showing good agreement with the experimentally measured values. Longer lifetimes of excitons in anatase lead to observed better photocatalytic activity of these two common TiO 2 phases. Our ab initio calculations of exciton lifetimes provide a new insight into understanding the correlation of the widely applicable packing factor model [X. Lin, J. Wu, X. Lue, Z. Shan, W. Wang and F. Huang, Phys. Chem. Chem. Phys., 2009, 11 , 10047-10052] with photocatalytic activity, and also a predictive and convenient tool for designing novel materials with potential applications in photonics and optoelectronics. Ab initio calculations show that the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/c8ta04140g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Accuracy ; Anatase ; Approximation ; Band structure ; Band structure of solids ; Bethe-Salpeter equation ; Catalytic activity ; Dependence ; Energy gap ; Excitons ; Mathematical analysis ; Optical activity ; Optoelectronics ; Photocatalysis ; Photonics ; Radiative lifetime ; Rutile ; Titanium dioxide</subject><ispartof>Journal of materials chemistry. 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A, Materials for energy and sustainability</title><description>This work presents the radiative lifetimes of photogenerated electron-hole (e-h) pairs in bulk anatase and rutile TiO 2 calculated by solving the Bethe-Salpeter equation (BSE) at the G 0 W 0 [F. Fuchs, J. Furthmüller, F. Bechstedt, M. Shishkin and G. Kresse, Phys. Rev. B: Condens. Matter Mater. Phys., 2007, 76 , 115109] level with Perdew-Burke-Ernzerhof (PBE) GGA as the starting point, an approach labeled as PBE- G 0 W 0 -BSE, where G 0 W 0 is the non-self-consistent GW approximation. The geometry optimization and the electronic ground state are determined using PBE. G 0 W 0 , considered as the "gold standard" for band structure calculations, provides band gap results of anatase and rutile in good agreement with experimental values. By solving BSE that surmounts the single-particle picture of individual quasielectron and quasihole excitation, the approach for calculating radiative lifetime shakes off the dependence on the band structure in DFT calculations and the renormalization factors in GW approximation. For anatase, the calculated intrinsic lifetime of the lowest optically active bright excitons turns out to be several microseconds, while that of rutile is a few picoseconds. Overall, the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile, showing good agreement with the experimentally measured values. Longer lifetimes of excitons in anatase lead to observed better photocatalytic activity of these two common TiO 2 phases. Our ab initio calculations of exciton lifetimes provide a new insight into understanding the correlation of the widely applicable packing factor model [X. Lin, J. Wu, X. Lue, Z. Shan, W. Wang and F. Huang, Phys. Chem. Chem. Phys., 2009, 11 , 10047-10052] with photocatalytic activity, and also a predictive and convenient tool for designing novel materials with potential applications in photonics and optoelectronics. Ab initio calculations show that the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile.</description><subject>Accuracy</subject><subject>Anatase</subject><subject>Approximation</subject><subject>Band structure</subject><subject>Band structure of solids</subject><subject>Bethe-Salpeter equation</subject><subject>Catalytic activity</subject><subject>Dependence</subject><subject>Energy gap</subject><subject>Excitons</subject><subject>Mathematical analysis</subject><subject>Optical activity</subject><subject>Optoelectronics</subject><subject>Photocatalysis</subject><subject>Photonics</subject><subject>Radiative lifetime</subject><subject>Rutile</subject><subject>Titanium dioxide</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEQhoMoWGov3oWAN2E1yebzWIpWoaCHevC0zGazNqXd1CQt9t93tVLnMsPLw7zwIHRNyT0lpXmwOgPhlJPPMzRgRJBCcSPPT7fWl2iU0pL0owmRxgzQx9si5GAhw2qfvcVgs9_5vMfQNTgvHI7QeOgzh1e-ddmvXcKhxe7b-hy6hHceehZDjX3nsw8YNpsYwC6u0EULq-RGf3uI3p8e55PnYvY6fZmMZ4XlTORCOKmgZEChAVEbZUxb1xJMQ50iSjIQsm2UsVpr1mhmtRO11hTAOWZKxcshuj3-7Wu_ti7lahm2sesrK0Y0F0RxSXrq7kjZGFKKrq020a8h7itKqh971UTPx7_2pj18c4Rjsifu3255AK0tbFc</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Hu, Linping</creator><creator>Xu, Chao</creator><creator>Peng, Liang</creator><creator>Gu, Feng Long</creator><creator>Yang, Weitao</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><scope>L7M</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0001-5576-2828</orcidid><orcidid>https://orcid.org/0000-0002-8141-6774</orcidid><orcidid>https://orcid.org/0000-0002-4043-2954</orcidid><orcidid>https://orcid.org/0000-0003-4965-0971</orcidid></search><sort><creationdate>2018</creationdate><title>Photocatalytic activity and the radiative lifetimes of excitons via an ab initio approach</title><author>Hu, Linping ; Xu, Chao ; Peng, Liang ; Gu, Feng Long ; Yang, Weitao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-5e67a32a1ada5b9799fbb6a9d1e70762a56fd79c8882d82c8e5b881aaee293743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Accuracy</topic><topic>Anatase</topic><topic>Approximation</topic><topic>Band structure</topic><topic>Band structure of solids</topic><topic>Bethe-Salpeter equation</topic><topic>Catalytic activity</topic><topic>Dependence</topic><topic>Energy gap</topic><topic>Excitons</topic><topic>Mathematical analysis</topic><topic>Optical activity</topic><topic>Optoelectronics</topic><topic>Photocatalysis</topic><topic>Photonics</topic><topic>Radiative lifetime</topic><topic>Rutile</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Linping</creatorcontrib><creatorcontrib>Xu, Chao</creatorcontrib><creatorcontrib>Peng, Liang</creatorcontrib><creatorcontrib>Gu, Feng Long</creatorcontrib><creatorcontrib>Yang, Weitao</creatorcontrib><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Journal of materials chemistry. 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B: Condens. Matter Mater. Phys., 2007, 76 , 115109] level with Perdew-Burke-Ernzerhof (PBE) GGA as the starting point, an approach labeled as PBE- G 0 W 0 -BSE, where G 0 W 0 is the non-self-consistent GW approximation. The geometry optimization and the electronic ground state are determined using PBE. G 0 W 0 , considered as the "gold standard" for band structure calculations, provides band gap results of anatase and rutile in good agreement with experimental values. By solving BSE that surmounts the single-particle picture of individual quasielectron and quasihole excitation, the approach for calculating radiative lifetime shakes off the dependence on the band structure in DFT calculations and the renormalization factors in GW approximation. For anatase, the calculated intrinsic lifetime of the lowest optically active bright excitons turns out to be several microseconds, while that of rutile is a few picoseconds. Overall, the e-h lifetimes of anatase are several orders of magnitude longer than those of rutile, showing good agreement with the experimentally measured values. Longer lifetimes of excitons in anatase lead to observed better photocatalytic activity of these two common TiO 2 phases. Our ab initio calculations of exciton lifetimes provide a new insight into understanding the correlation of the widely applicable packing factor model [X. Lin, J. Wu, X. Lue, Z. Shan, W. Wang and F. Huang, Phys. Chem. Chem. Phys., 2009, 11 , 10047-10052] with photocatalytic activity, and also a predictive and convenient tool for designing novel materials with potential applications in photonics and optoelectronics. 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subjects Accuracy
Anatase
Approximation
Band structure
Band structure of solids
Bethe-Salpeter equation
Catalytic activity
Dependence
Energy gap
Excitons
Mathematical analysis
Optical activity
Optoelectronics
Photocatalysis
Photonics
Radiative lifetime
Rutile
Titanium dioxide
title Photocatalytic activity and the radiative lifetimes of excitons via an ab initio approach
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