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Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells
Sebastian Pont,
Daniel Bryant,
Chieh-Ting Lin,
Nicholas Aristidou,
Scot Wheeler,
Xuerui Ma,
Robert Godin,
Saif A. Haque,
James Durrant
J. Mater. Chem. A, Volume: 5, Issue: 20, Pages: 9553 - 9560
Swansea University Author: James Durrant
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DOI (Published version): 10.1039/C7TA00058H
Abstract
The rapid development of organic–inorganic lead halide perovskites has resulted in high efficiency photovoltaic devices. However the susceptibility of these devices to degradation under environmental stress has so far hindered commercial development, requiring for example expensive device encapsulat...
Published in: | J. Mater. Chem. A |
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ISSN: | 2050-7488 2050-7496 |
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2017
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URI: | https://cronfa.swan.ac.uk/Record/cronfa34708 |
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<?xml version="1.0"?><rfc1807><datestamp>2017-07-20T10:10:59.8589137</datestamp><bib-version>v2</bib-version><id>34708</id><entry>2017-07-20</entry><title>Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells</title><swanseaauthors><author><sid>f3dd64bc260e5c07adfa916c27dbd58a</sid><ORCID>0000-0001-8353-7345</ORCID><firstname>James</firstname><surname>Durrant</surname><name>James Durrant</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2017-07-20</date><deptcode>MTLS</deptcode><abstract>The rapid development of organic–inorganic lead halide perovskites has resulted in high efficiency photovoltaic devices. However the susceptibility of these devices to degradation under environmental stress has so far hindered commercial development, requiring for example expensive device encapsulation. Herein, we have investigated the stability of CH3NH3Pb(I1−xBrx)3 [x = 0–1] thin films and solar cells under controlled humidity, light, and oxygen conditions. We show that higher bromide ratios increase tolerance to moisture, with x = 1 thin films being stable to 120 h of moisture stress. Under light and dry air, partial bromide (x < 1) substitution does not enhance film stability significantly, with the corresponding solar cells degrading within two hours. In contrast, CH3NH3PbBr3 films show excellent stability, with device stability being limited by the organic interlayer. For these x = 1 films, we show that charge carriers are quenched in the presence of oxygen and form superoxide; however in contrast to perovskites containing iodide, this superoxide does not degrade the crystal. Our observations show that iodide limits the oxygen and light stability of CH3NH3Pb(I1−xBrx)3 perovskites, but that CH3NH3PbBr3 provides an opportunity to develop inherently stable high voltage photovoltaic devices and 4-terminal tandem solar cells.</abstract><type>Journal Article</type><journal>J. Mater. Chem. A</journal><volume>5</volume><journalNumber>20</journalNumber><paginationStart>9553</paginationStart><paginationEnd>9560</paginationEnd><publisher/><issnPrint>2050-7488</issnPrint><issnElectronic>2050-7496</issnElectronic><keywords/><publishedDay>31</publishedDay><publishedMonth>12</publishedMonth><publishedYear>2017</publishedYear><publishedDate>2017-12-31</publishedDate><doi>10.1039/C7TA00058H</doi><url/><notes/><college>COLLEGE NANME</college><department>Materials Science and Engineering</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>MTLS</DepartmentCode><institution>Swansea University</institution><apcterm/><lastEdited>2017-07-20T10:10:59.8589137</lastEdited><Created>2017-07-20T10:05:54.9380189</Created><path><level id="1">Faculty of Science and Engineering</level><level id="2">School of Engineering and Applied Sciences - Materials Science and Engineering</level></path><authors><author><firstname>Sebastian</firstname><surname>Pont</surname><order>1</order></author><author><firstname>Daniel</firstname><surname>Bryant</surname><order>2</order></author><author><firstname>Chieh-Ting</firstname><surname>Lin</surname><order>3</order></author><author><firstname>Nicholas</firstname><surname>Aristidou</surname><order>4</order></author><author><firstname>Scot</firstname><surname>Wheeler</surname><order>5</order></author><author><firstname>Xuerui</firstname><surname>Ma</surname><order>6</order></author><author><firstname>Robert</firstname><surname>Godin</surname><order>7</order></author><author><firstname>Saif A.</firstname><surname>Haque</surname><order>8</order></author><author><firstname>James</firstname><surname>Durrant</surname><orcid>0000-0001-8353-7345</orcid><order>9</order></author></authors><documents/><OutputDurs/></rfc1807> |
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2017-07-20T10:10:59.8589137 v2 34708 2017-07-20 Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells f3dd64bc260e5c07adfa916c27dbd58a 0000-0001-8353-7345 James Durrant James Durrant true false 2017-07-20 MTLS The rapid development of organic–inorganic lead halide perovskites has resulted in high efficiency photovoltaic devices. However the susceptibility of these devices to degradation under environmental stress has so far hindered commercial development, requiring for example expensive device encapsulation. Herein, we have investigated the stability of CH3NH3Pb(I1−xBrx)3 [x = 0–1] thin films and solar cells under controlled humidity, light, and oxygen conditions. We show that higher bromide ratios increase tolerance to moisture, with x = 1 thin films being stable to 120 h of moisture stress. Under light and dry air, partial bromide (x < 1) substitution does not enhance film stability significantly, with the corresponding solar cells degrading within two hours. In contrast, CH3NH3PbBr3 films show excellent stability, with device stability being limited by the organic interlayer. For these x = 1 films, we show that charge carriers are quenched in the presence of oxygen and form superoxide; however in contrast to perovskites containing iodide, this superoxide does not degrade the crystal. Our observations show that iodide limits the oxygen and light stability of CH3NH3Pb(I1−xBrx)3 perovskites, but that CH3NH3PbBr3 provides an opportunity to develop inherently stable high voltage photovoltaic devices and 4-terminal tandem solar cells. Journal Article J. Mater. Chem. A 5 20 9553 9560 2050-7488 2050-7496 31 12 2017 2017-12-31 10.1039/C7TA00058H COLLEGE NANME Materials Science and Engineering COLLEGE CODE MTLS Swansea University 2017-07-20T10:10:59.8589137 2017-07-20T10:05:54.9380189 Faculty of Science and Engineering School of Engineering and Applied Sciences - Materials Science and Engineering Sebastian Pont 1 Daniel Bryant 2 Chieh-Ting Lin 3 Nicholas Aristidou 4 Scot Wheeler 5 Xuerui Ma 6 Robert Godin 7 Saif A. Haque 8 James Durrant 0000-0001-8353-7345 9 |
title |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
spellingShingle |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells James Durrant |
title_short |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
title_full |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
title_fullStr |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
title_full_unstemmed |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
title_sort |
Tuning CH3NH3Pb(I1−xBrx)3 perovskite oxygen stability in thin films and solar cells |
author_id_str_mv |
f3dd64bc260e5c07adfa916c27dbd58a |
author_id_fullname_str_mv |
f3dd64bc260e5c07adfa916c27dbd58a_***_James Durrant |
author |
James Durrant |
author2 |
Sebastian Pont Daniel Bryant Chieh-Ting Lin Nicholas Aristidou Scot Wheeler Xuerui Ma Robert Godin Saif A. Haque James Durrant |
format |
Journal article |
container_title |
J. Mater. Chem. A |
container_volume |
5 |
container_issue |
20 |
container_start_page |
9553 |
publishDate |
2017 |
institution |
Swansea University |
issn |
2050-7488 2050-7496 |
doi_str_mv |
10.1039/C7TA00058H |
college_str |
Faculty of Science and Engineering |
hierarchytype |
|
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facultyofscienceandengineering |
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Faculty of Science and Engineering |
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facultyofscienceandengineering |
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Faculty of Science and Engineering |
department_str |
School of Engineering and Applied Sciences - Materials Science and Engineering{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Materials Science and Engineering |
document_store_str |
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description |
The rapid development of organic–inorganic lead halide perovskites has resulted in high efficiency photovoltaic devices. However the susceptibility of these devices to degradation under environmental stress has so far hindered commercial development, requiring for example expensive device encapsulation. Herein, we have investigated the stability of CH3NH3Pb(I1−xBrx)3 [x = 0–1] thin films and solar cells under controlled humidity, light, and oxygen conditions. We show that higher bromide ratios increase tolerance to moisture, with x = 1 thin films being stable to 120 h of moisture stress. Under light and dry air, partial bromide (x < 1) substitution does not enhance film stability significantly, with the corresponding solar cells degrading within two hours. In contrast, CH3NH3PbBr3 films show excellent stability, with device stability being limited by the organic interlayer. For these x = 1 films, we show that charge carriers are quenched in the presence of oxygen and form superoxide; however in contrast to perovskites containing iodide, this superoxide does not degrade the crystal. Our observations show that iodide limits the oxygen and light stability of CH3NH3Pb(I1−xBrx)3 perovskites, but that CH3NH3PbBr3 provides an opportunity to develop inherently stable high voltage photovoltaic devices and 4-terminal tandem solar cells. |
published_date |
2017-12-31T03:43:04Z |
_version_ |
1763752001978499072 |
score |
11.035655 |