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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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 |
format | Article |
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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><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. A, Materials for energy and sustainability, 2018, Vol.6 (31), p.1527-1532</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-5e67a32a1ada5b9799fbb6a9d1e70762a56fd79c8882d82c8e5b881aaee293743</citedby><cites>FETCH-LOGICAL-c425t-5e67a32a1ada5b9799fbb6a9d1e70762a56fd79c8882d82c8e5b881aaee293743</cites><orcidid>0000-0001-5576-2828 ; 0000-0002-8141-6774 ; 0000-0002-4043-2954 ; 0000-0003-4965-0971</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids></links><search><creatorcontrib>Hu, Linping</creatorcontrib><creatorcontrib>Xu, Chao</creatorcontrib><creatorcontrib>Peng, Liang</creatorcontrib><creatorcontrib>Gu, Feng Long</creatorcontrib><creatorcontrib>Yang, Weitao</creatorcontrib><title>Photocatalytic activity and the radiative lifetimes of excitons via an ab initio approach</title><title>Journal of materials chemistry. 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 & 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. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Linping</au><au>Xu, Chao</au><au>Peng, Liang</au><au>Gu, Feng Long</au><au>Yang, Weitao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photocatalytic activity and the radiative lifetimes of excitons via an ab initio approach</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2018</date><risdate>2018</risdate><volume>6</volume><issue>31</issue><spage>1527</spage><epage>1532</epage><pages>1527-1532</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>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.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c8ta04140g</doi><tpages>6</tpages><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></addata></record> |
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language | eng |
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source | Royal Society Of Chemistry Journals 2008- |
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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