Optical and Electronic Properties of Pyrite Nanocrystal Thin Films: the Role of Ligands
Pyrite nanocrystals are currently considered as a promising material for large scale photovoltaic applications due to their non‐toxicity and large abundance. While scalable synthetic routes for phase‐pure and shape controlled colloidal pyrite nanocrystals have been reported, their use in solar cells...
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Veröffentlicht in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2014-03, Vol.10 (6), p.1194-1201 |
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description | Pyrite nanocrystals are currently considered as a promising material for large scale photovoltaic applications due to their non‐toxicity and large abundance. While scalable synthetic routes for phase‐pure and shape controlled colloidal pyrite nanocrystals have been reported, their use in solar cells has been hampered by the detrimental effects of their surface defects. Here, we report a systematic study of optical and electronic properties of pyrite nanocrystal thin films employing a series of different ligands varying both the anchor and bridging group. The effect of the ligands on the optical and electronic properties is investigated by UV‐vis/NIR absorption spectroscopy, current voltage characteristic measurements and surface photovoltage spectroscopy. We find that the optical absorption is mainly determined by the anchor group. The absorption onset in the thin films shifts up to ∼100 meV to the red. This is attributed to changes in the dielectric environment induced by different anchors. The conductivity and photoconductivity, on the other hand, are determined by combined effects of anchor and bridging group, which modify the effective hopping barrier. Employing different ligands, the differential conductance varies over four orders of magnitude. The largest redshift and differential conductance are observed for ammonium sulfides and thiolated aromatic linkers. Pyridine and long chain amines, on the other hand, lead to smaller modifications. Our findings highlight the importance of surface functionalization and interparticle electronic coupling in the use of pyrite nanocrystals for photovoltaic devices.
The influence of ligand anchor and bridging groups on the optical and electronic properties of pyrite nanocrystal thin films is investigated systematically. The thin film absorption onset shifts up to 100 meV to the red and the differential conductance varies over four orders of magnitude for the different ligands with ammonium sulfides and thiolated aromatic linkers showing the largest effects. |
doi_str_mv | 10.1002/smll.201302333 |
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The influence of ligand anchor and bridging groups on the optical and electronic properties of pyrite nanocrystal thin films is investigated systematically. The thin film absorption onset shifts up to 100 meV to the red and the differential conductance varies over four orders of magnitude for the different ligands with ammonium sulfides and thiolated aromatic linkers showing the largest effects.</description><identifier>ISSN: 1613-6810</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.201302333</identifier><identifier>PMID: 24395590</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Anchors ; Bridging ; Conductivity ; Electronic properties ; iron sulfides ; Ligands ; Nanocrystals ; Nanotechnology ; Optical properties ; Pyrite ; semiconductor nanocrystal solids ; solar cells ; Spectrum analysis ; surface photo voltage spectroscopy ; surface states ; Thin films</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2014-03, Vol.10 (6), p.1194-1201</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4853-55802ae7ef3c116562240c10f5885ff48b63453b225016af2a71aa091cb09b03</citedby><cites>FETCH-LOGICAL-c4853-55802ae7ef3c116562240c10f5885ff48b63453b225016af2a71aa091cb09b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsmll.201302333$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsmll.201302333$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24395590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Dittrich, Thomas</creatorcontrib><creatorcontrib>Jäckel, Frank</creatorcontrib><creatorcontrib>Feldmann, Jochen</creatorcontrib><title>Optical and Electronic Properties of Pyrite Nanocrystal Thin Films: the Role of Ligands</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>Pyrite nanocrystals are currently considered as a promising material for large scale photovoltaic applications due to their non‐toxicity and large abundance. While scalable synthetic routes for phase‐pure and shape controlled colloidal pyrite nanocrystals have been reported, their use in solar cells has been hampered by the detrimental effects of their surface defects. Here, we report a systematic study of optical and electronic properties of pyrite nanocrystal thin films employing a series of different ligands varying both the anchor and bridging group. The effect of the ligands on the optical and electronic properties is investigated by UV‐vis/NIR absorption spectroscopy, current voltage characteristic measurements and surface photovoltage spectroscopy. We find that the optical absorption is mainly determined by the anchor group. The absorption onset in the thin films shifts up to ∼100 meV to the red. This is attributed to changes in the dielectric environment induced by different anchors. The conductivity and photoconductivity, on the other hand, are determined by combined effects of anchor and bridging group, which modify the effective hopping barrier. Employing different ligands, the differential conductance varies over four orders of magnitude. The largest redshift and differential conductance are observed for ammonium sulfides and thiolated aromatic linkers. Pyridine and long chain amines, on the other hand, lead to smaller modifications. Our findings highlight the importance of surface functionalization and interparticle electronic coupling in the use of pyrite nanocrystals for photovoltaic devices.
The influence of ligand anchor and bridging groups on the optical and electronic properties of pyrite nanocrystal thin films is investigated systematically. The thin film absorption onset shifts up to 100 meV to the red and the differential conductance varies over four orders of magnitude for the different ligands with ammonium sulfides and thiolated aromatic linkers showing the largest effects.</description><subject>Anchors</subject><subject>Bridging</subject><subject>Conductivity</subject><subject>Electronic properties</subject><subject>iron sulfides</subject><subject>Ligands</subject><subject>Nanocrystals</subject><subject>Nanotechnology</subject><subject>Optical properties</subject><subject>Pyrite</subject><subject>semiconductor nanocrystal solids</subject><subject>solar cells</subject><subject>Spectrum analysis</subject><subject>surface photo voltage spectroscopy</subject><subject>surface states</subject><subject>Thin films</subject><issn>1613-6810</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0c1rFDEYBvAgiq3Vq0cJePEy6_vmYz68ydLdCmNbdKHFS8ikGZuamWyTWXT_-2bZuogXPSWH3_OQ8BDyGmGGAOx9GryfMUAOjHP-hBxjibwoa9Y8PdwRjsiLlO4AODJRPSdHTPBGygaOydXFenJGe6rHG3rqrZliGJ2hlzGsbZycTTT09HIb3WTpuR6Dids0Zb-6dSNdOD-kD3S6tfRL8HZHW_c9V6WX5FmvfbKvHs8TslqcruZnRXux_DT_2BZG1JIXUtbAtK1szw1iKUvGBBiEXta17HtRdyUXkneMScBS90xXqDU0aDpoOuAn5N2-dh3D_camSQ0uGeu9Hm3YJIVSoGCsFtV_UARElHWZ6du_6F3YxDH_IytoeFNWHLOa7ZWJIaVoe7WObtBxqxDUbhy1G0cdxsmBN4-1m26wNwf-e40Mmj346bzd_qNOff3ctn-WF_usS5P9dcjq-EPl11ZSXZ0v1fVCfpu3161a8gflXqfn</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Li, Wei</creator><creator>Dittrich, Thomas</creator><creator>Jäckel, Frank</creator><creator>Feldmann, Jochen</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>F28</scope><scope>FR3</scope></search><sort><creationdate>20140301</creationdate><title>Optical and Electronic Properties of Pyrite Nanocrystal Thin Films: the Role of Ligands</title><author>Li, Wei ; Dittrich, Thomas ; Jäckel, Frank ; Feldmann, Jochen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4853-55802ae7ef3c116562240c10f5885ff48b63453b225016af2a71aa091cb09b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Anchors</topic><topic>Bridging</topic><topic>Conductivity</topic><topic>Electronic properties</topic><topic>iron sulfides</topic><topic>Ligands</topic><topic>Nanocrystals</topic><topic>Nanotechnology</topic><topic>Optical properties</topic><topic>Pyrite</topic><topic>semiconductor nanocrystal solids</topic><topic>solar cells</topic><topic>Spectrum analysis</topic><topic>surface photo voltage spectroscopy</topic><topic>surface states</topic><topic>Thin films</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Dittrich, Thomas</creatorcontrib><creatorcontrib>Jäckel, Frank</creatorcontrib><creatorcontrib>Feldmann, Jochen</creatorcontrib><collection>Istex</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Wei</au><au>Dittrich, Thomas</au><au>Jäckel, Frank</au><au>Feldmann, Jochen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optical and Electronic Properties of Pyrite Nanocrystal Thin Films: the Role of Ligands</atitle><jtitle>Small (Weinheim an der Bergstrasse, Germany)</jtitle><addtitle>Small</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>10</volume><issue>6</issue><spage>1194</spage><epage>1201</epage><pages>1194-1201</pages><issn>1613-6810</issn><eissn>1613-6829</eissn><abstract>Pyrite nanocrystals are currently considered as a promising material for large scale photovoltaic applications due to their non‐toxicity and large abundance. While scalable synthetic routes for phase‐pure and shape controlled colloidal pyrite nanocrystals have been reported, their use in solar cells has been hampered by the detrimental effects of their surface defects. Here, we report a systematic study of optical and electronic properties of pyrite nanocrystal thin films employing a series of different ligands varying both the anchor and bridging group. The effect of the ligands on the optical and electronic properties is investigated by UV‐vis/NIR absorption spectroscopy, current voltage characteristic measurements and surface photovoltage spectroscopy. We find that the optical absorption is mainly determined by the anchor group. The absorption onset in the thin films shifts up to ∼100 meV to the red. This is attributed to changes in the dielectric environment induced by different anchors. The conductivity and photoconductivity, on the other hand, are determined by combined effects of anchor and bridging group, which modify the effective hopping barrier. Employing different ligands, the differential conductance varies over four orders of magnitude. The largest redshift and differential conductance are observed for ammonium sulfides and thiolated aromatic linkers. Pyridine and long chain amines, on the other hand, lead to smaller modifications. Our findings highlight the importance of surface functionalization and interparticle electronic coupling in the use of pyrite nanocrystals for photovoltaic devices.
The influence of ligand anchor and bridging groups on the optical and electronic properties of pyrite nanocrystal thin films is investigated systematically. The thin film absorption onset shifts up to 100 meV to the red and the differential conductance varies over four orders of magnitude for the different ligands with ammonium sulfides and thiolated aromatic linkers showing the largest effects.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>24395590</pmid><doi>10.1002/smll.201302333</doi><tpages>8</tpages></addata></record> |
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subjects | Anchors Bridging Conductivity Electronic properties iron sulfides Ligands Nanocrystals Nanotechnology Optical properties Pyrite semiconductor nanocrystal solids solar cells Spectrum analysis surface photo voltage spectroscopy surface states Thin films |
title | Optical and Electronic Properties of Pyrite Nanocrystal Thin Films: the Role of Ligands |
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