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Phase segregation due to ion migration in all-inorganic mixed-halide perovskite nanocrystals
Semiconductor mixed-halide perovskites featured with a tunable energy bandgap are ideal candidates for light absorbers in tandem solar cells as well as fluorescent materials in light-emitting diodes and nanoscale lasers. These device advancements are currently hindered by the light-induced phase seg...
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Published in: | Nature communications 2019-03, Vol.10 (1), p.1088-1088, Article 1088 |
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description | Semiconductor mixed-halide perovskites featured with a tunable energy bandgap are ideal candidates for light absorbers in tandem solar cells as well as fluorescent materials in light-emitting diodes and nanoscale lasers. These device advancements are currently hindered by the light-induced phase segregation effect, whereby ion migration would yield smaller-bandgap domains with red-shifted photoluminescence. Here we show that upon laser excitation all-inorganic mixed-halide nanocrystals unexpectedly exhibit a blue shift in the photoluminescence peak that can revert back in the dark, thus depicting the processes of ion migration out of and back to the originally excited nanocrystals. Interestingly, this reversible photoluminescence shift can also be induced by electrical biasing of mixed-halide nanocrystals without the injection of charge carriers. The above findings suggest that it is the local electric field that breaks the ionic bonds in mixed-halide nanocrystals, which could be a universal origin for light-induced phase segregation observed in other mixed-halide perovskite materials.
Mixed-halide perovskites possess excellent semiconductor properties but suffer severely from notorious light-induced phase segregation effect. Here Zhang et al. employ simple photoluminescence measurements to link the effect to the local electric field induced ion migration process. |
doi_str_mv | 10.1038/s41467-019-09047-7 |
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Mixed-halide perovskites possess excellent semiconductor properties but suffer severely from notorious light-induced phase segregation effect. Here Zhang et al. employ simple photoluminescence measurements to link the effect to the local electric field induced ion migration process.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-019-09047-7</identifier><identifier>PMID: 30842434</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>140/125 ; 639/301/1019 ; 639/301/357 ; 639/624/400 ; 639/925/357 ; Blue shift ; Charge injection ; Crystals ; Current carriers ; Domains ; Electric fields ; Energy gap ; Fluorescence ; Humanities and Social Sciences ; Ion migration ; Lasers ; Luminescence ; multidisciplinary ; Nanocrystals ; Organic light emitting diodes ; Perovskites ; Photoluminescence ; Photons ; Photovoltaic cells ; Science ; Science (multidisciplinary) ; Solar cells</subject><ispartof>Nature communications, 2019-03, Vol.10 (1), p.1088-1088, Article 1088</ispartof><rights>The Author(s) 2019</rights><rights>This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c606t-f9d97b001933957b59a97a9d688c8d46b360e66f6a7707f72c0174d831d910913</citedby><cites>FETCH-LOGICAL-c606t-f9d97b001933957b59a97a9d688c8d46b360e66f6a7707f72c0174d831d910913</cites><orcidid>0000-0001-5354-6718</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2188582224/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2188582224?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30842434$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Huichao</creatorcontrib><creatorcontrib>Fu, Xu</creatorcontrib><creatorcontrib>Tang, Ying</creatorcontrib><creatorcontrib>Wang, Hua</creatorcontrib><creatorcontrib>Zhang, Chunfeng</creatorcontrib><creatorcontrib>Yu, William W.</creatorcontrib><creatorcontrib>Wang, Xiaoyong</creatorcontrib><creatorcontrib>Zhang, Yu</creatorcontrib><creatorcontrib>Xiao, Min</creatorcontrib><title>Phase segregation due to ion migration in all-inorganic mixed-halide perovskite nanocrystals</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>Semiconductor mixed-halide perovskites featured with a tunable energy bandgap are ideal candidates for light absorbers in tandem solar cells as well as fluorescent materials in light-emitting diodes and nanoscale lasers. These device advancements are currently hindered by the light-induced phase segregation effect, whereby ion migration would yield smaller-bandgap domains with red-shifted photoluminescence. Here we show that upon laser excitation all-inorganic mixed-halide nanocrystals unexpectedly exhibit a blue shift in the photoluminescence peak that can revert back in the dark, thus depicting the processes of ion migration out of and back to the originally excited nanocrystals. Interestingly, this reversible photoluminescence shift can also be induced by electrical biasing of mixed-halide nanocrystals without the injection of charge carriers. The above findings suggest that it is the local electric field that breaks the ionic bonds in mixed-halide nanocrystals, which could be a universal origin for light-induced phase segregation observed in other mixed-halide perovskite materials.
Mixed-halide perovskites possess excellent semiconductor properties but suffer severely from notorious light-induced phase segregation effect. Here Zhang et al. employ simple photoluminescence measurements to link the effect to the local electric field induced ion migration process.</description><subject>140/125</subject><subject>639/301/1019</subject><subject>639/301/357</subject><subject>639/624/400</subject><subject>639/925/357</subject><subject>Blue shift</subject><subject>Charge injection</subject><subject>Crystals</subject><subject>Current carriers</subject><subject>Domains</subject><subject>Electric fields</subject><subject>Energy gap</subject><subject>Fluorescence</subject><subject>Humanities and Social Sciences</subject><subject>Ion migration</subject><subject>Lasers</subject><subject>Luminescence</subject><subject>multidisciplinary</subject><subject>Nanocrystals</subject><subject>Organic light emitting diodes</subject><subject>Perovskites</subject><subject>Photoluminescence</subject><subject>Photons</subject><subject>Photovoltaic cells</subject><subject>Science</subject><subject>Science 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Commun</addtitle><date>2019-03-06</date><risdate>2019</risdate><volume>10</volume><issue>1</issue><spage>1088</spage><epage>1088</epage><pages>1088-1088</pages><artnum>1088</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Semiconductor mixed-halide perovskites featured with a tunable energy bandgap are ideal candidates for light absorbers in tandem solar cells as well as fluorescent materials in light-emitting diodes and nanoscale lasers. These device advancements are currently hindered by the light-induced phase segregation effect, whereby ion migration would yield smaller-bandgap domains with red-shifted photoluminescence. Here we show that upon laser excitation all-inorganic mixed-halide nanocrystals unexpectedly exhibit a blue shift in the photoluminescence peak that can revert back in the dark, thus depicting the processes of ion migration out of and back to the originally excited nanocrystals. Interestingly, this reversible photoluminescence shift can also be induced by electrical biasing of mixed-halide nanocrystals without the injection of charge carriers. The above findings suggest that it is the local electric field that breaks the ionic bonds in mixed-halide nanocrystals, which could be a universal origin for light-induced phase segregation observed in other mixed-halide perovskite materials.
Mixed-halide perovskites possess excellent semiconductor properties but suffer severely from notorious light-induced phase segregation effect. Here Zhang et al. employ simple photoluminescence measurements to link the effect to the local electric field induced ion migration process.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30842434</pmid><doi>10.1038/s41467-019-09047-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5354-6718</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 140/125 639/301/1019 639/301/357 639/624/400 639/925/357 Blue shift Charge injection Crystals Current carriers Domains Electric fields Energy gap Fluorescence Humanities and Social Sciences Ion migration Lasers Luminescence multidisciplinary Nanocrystals Organic light emitting diodes Perovskites Photoluminescence Photons Photovoltaic cells Science Science (multidisciplinary) Solar cells |
title | Phase segregation due to ion migration in all-inorganic mixed-halide perovskite nanocrystals |
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