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Poly(4-styrenesulfonate)-induced sulfur vacancy self-healing strategy for monolayer MoS 2 homojunction photodiode
We establish a powerful poly(4-styrenesulfonate) (PSS)-treated strategy for sulfur vacancy healing in monolayer MoS to precisely and steadily tune its electronic state. The self-healing mechanism, in which the sulfur vacancies are healed spontaneously by the sulfur adatom clusters on the MoS surface...
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Published in: | Nature communications 2017-06, Vol.8, p.15881 |
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container_title | Nature communications |
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creator | Zhang, Xiankun Liao, Qingliang Liu, Shuo Kang, Zhuo Zhang, Zheng Du, Junli Li, Feng Zhang, Shuhao Xiao, Jiankun Liu, Baishan Ou, Yang Liu, Xiaozhi Gu, Lin Zhang, Yue |
description | We establish a powerful poly(4-styrenesulfonate) (PSS)-treated strategy for sulfur vacancy healing in monolayer MoS
to precisely and steadily tune its electronic state. The self-healing mechanism, in which the sulfur vacancies are healed spontaneously by the sulfur adatom clusters on the MoS
surface through a PSS-induced hydrogenation process, is proposed and demonstrated systematically. The electron concentration of the self-healed MoS
dramatically decreased by 643 times, leading to a work function enhancement of ∼150 meV. This strategy is employed to fabricate a high performance lateral monolayer MoS
homojunction which presents a perfect rectifying behaviour, excellent photoresponsivity of ∼308 mA W
and outstanding air-stability after two months. Unlike previous chemical doping, the lattice defect-induced local fields are eliminated during the process of the sulfur vacancy self-healing to largely improve the homojunction performance. Our findings demonstrate a promising and facile strategy in 2D material electronic state modulation for the development of next-generation electronics and optoelectronics. |
doi_str_mv | 10.1038/ncomms15881 |
format | article |
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to precisely and steadily tune its electronic state. The self-healing mechanism, in which the sulfur vacancies are healed spontaneously by the sulfur adatom clusters on the MoS
surface through a PSS-induced hydrogenation process, is proposed and demonstrated systematically. The electron concentration of the self-healed MoS
dramatically decreased by 643 times, leading to a work function enhancement of ∼150 meV. This strategy is employed to fabricate a high performance lateral monolayer MoS
homojunction which presents a perfect rectifying behaviour, excellent photoresponsivity of ∼308 mA W
and outstanding air-stability after two months. Unlike previous chemical doping, the lattice defect-induced local fields are eliminated during the process of the sulfur vacancy self-healing to largely improve the homojunction performance. Our findings demonstrate a promising and facile strategy in 2D material electronic state modulation for the development of next-generation electronics and optoelectronics.</description><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/ncomms15881</identifier><identifier>PMID: 28639620</identifier><language>eng</language><publisher>England</publisher><ispartof>Nature communications, 2017-06, Vol.8, p.15881</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28639620$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Xiankun</creatorcontrib><creatorcontrib>Liao, Qingliang</creatorcontrib><creatorcontrib>Liu, Shuo</creatorcontrib><creatorcontrib>Kang, Zhuo</creatorcontrib><creatorcontrib>Zhang, Zheng</creatorcontrib><creatorcontrib>Du, Junli</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Zhang, Shuhao</creatorcontrib><creatorcontrib>Xiao, Jiankun</creatorcontrib><creatorcontrib>Liu, Baishan</creatorcontrib><creatorcontrib>Ou, Yang</creatorcontrib><creatorcontrib>Liu, Xiaozhi</creatorcontrib><creatorcontrib>Gu, Lin</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><title>Poly(4-styrenesulfonate)-induced sulfur vacancy self-healing strategy for monolayer MoS 2 homojunction photodiode</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><description>We establish a powerful poly(4-styrenesulfonate) (PSS)-treated strategy for sulfur vacancy healing in monolayer MoS
to precisely and steadily tune its electronic state. The self-healing mechanism, in which the sulfur vacancies are healed spontaneously by the sulfur adatom clusters on the MoS
surface through a PSS-induced hydrogenation process, is proposed and demonstrated systematically. The electron concentration of the self-healed MoS
dramatically decreased by 643 times, leading to a work function enhancement of ∼150 meV. This strategy is employed to fabricate a high performance lateral monolayer MoS
homojunction which presents a perfect rectifying behaviour, excellent photoresponsivity of ∼308 mA W
and outstanding air-stability after two months. Unlike previous chemical doping, the lattice defect-induced local fields are eliminated during the process of the sulfur vacancy self-healing to largely improve the homojunction performance. Our findings demonstrate a promising and facile strategy in 2D material electronic state modulation for the development of next-generation electronics and optoelectronics.</description><issn>2041-1723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo1j89LwzAcxYMgbsydvEuOeojmZ5ccZegUJgrzPtI0WTvafGvSCv3vnajv8uDD4wMPoStG7xgV-j466LrMlNbsDM05lYywFRcztMz5SE8RhmkpL9CM60KYgtM5-nyHdrqRJA9T8tHnsQ0Q7eBvSROr0fkK_6Ax4S_rbHQTzr4NpPa2beIB5yGdtocJB0i4gwitnXzCr7DDHNfQwXGMbmgg4r6GAaoGKn-JzoNts1_-9QLtnh4_1s9k-7Z5WT9sSW_EQMrSGmeVEoZq7oMslZHcSa5W3vlSccZFkKqwRTDCaMuVC6Wl0q1EsCIEsUDXv9Z-LDtf7fvUdDZN-__n4huGDVzn</recordid><startdate>20170622</startdate><enddate>20170622</enddate><creator>Zhang, Xiankun</creator><creator>Liao, Qingliang</creator><creator>Liu, Shuo</creator><creator>Kang, Zhuo</creator><creator>Zhang, Zheng</creator><creator>Du, Junli</creator><creator>Li, Feng</creator><creator>Zhang, Shuhao</creator><creator>Xiao, Jiankun</creator><creator>Liu, Baishan</creator><creator>Ou, Yang</creator><creator>Liu, Xiaozhi</creator><creator>Gu, Lin</creator><creator>Zhang, Yue</creator><scope>NPM</scope></search><sort><creationdate>20170622</creationdate><title>Poly(4-styrenesulfonate)-induced sulfur vacancy self-healing strategy for monolayer MoS 2 homojunction photodiode</title><author>Zhang, Xiankun ; Liao, Qingliang ; Liu, Shuo ; Kang, Zhuo ; Zhang, Zheng ; Du, Junli ; Li, Feng ; Zhang, Shuhao ; Xiao, Jiankun ; Liu, Baishan ; Ou, Yang ; Liu, Xiaozhi ; Gu, Lin ; Zhang, Yue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p93t-bba9ca5539082ef4b5942c4257eceb52123f456a6f9398a25cfba04c73fa3ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xiankun</creatorcontrib><creatorcontrib>Liao, Qingliang</creatorcontrib><creatorcontrib>Liu, Shuo</creatorcontrib><creatorcontrib>Kang, Zhuo</creatorcontrib><creatorcontrib>Zhang, Zheng</creatorcontrib><creatorcontrib>Du, Junli</creatorcontrib><creatorcontrib>Li, Feng</creatorcontrib><creatorcontrib>Zhang, Shuhao</creatorcontrib><creatorcontrib>Xiao, Jiankun</creatorcontrib><creatorcontrib>Liu, Baishan</creatorcontrib><creatorcontrib>Ou, Yang</creatorcontrib><creatorcontrib>Liu, Xiaozhi</creatorcontrib><creatorcontrib>Gu, Lin</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><collection>PubMed</collection><jtitle>Nature communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xiankun</au><au>Liao, Qingliang</au><au>Liu, Shuo</au><au>Kang, Zhuo</au><au>Zhang, Zheng</au><au>Du, Junli</au><au>Li, Feng</au><au>Zhang, Shuhao</au><au>Xiao, Jiankun</au><au>Liu, Baishan</au><au>Ou, Yang</au><au>Liu, Xiaozhi</au><au>Gu, Lin</au><au>Zhang, Yue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Poly(4-styrenesulfonate)-induced sulfur vacancy self-healing strategy for monolayer MoS 2 homojunction photodiode</atitle><jtitle>Nature communications</jtitle><addtitle>Nat Commun</addtitle><date>2017-06-22</date><risdate>2017</risdate><volume>8</volume><spage>15881</spage><pages>15881-</pages><eissn>2041-1723</eissn><abstract>We establish a powerful poly(4-styrenesulfonate) (PSS)-treated strategy for sulfur vacancy healing in monolayer MoS
to precisely and steadily tune its electronic state. The self-healing mechanism, in which the sulfur vacancies are healed spontaneously by the sulfur adatom clusters on the MoS
surface through a PSS-induced hydrogenation process, is proposed and demonstrated systematically. The electron concentration of the self-healed MoS
dramatically decreased by 643 times, leading to a work function enhancement of ∼150 meV. This strategy is employed to fabricate a high performance lateral monolayer MoS
homojunction which presents a perfect rectifying behaviour, excellent photoresponsivity of ∼308 mA W
and outstanding air-stability after two months. Unlike previous chemical doping, the lattice defect-induced local fields are eliminated during the process of the sulfur vacancy self-healing to largely improve the homojunction performance. Our findings demonstrate a promising and facile strategy in 2D material electronic state modulation for the development of next-generation electronics and optoelectronics.</abstract><cop>England</cop><pmid>28639620</pmid><doi>10.1038/ncomms15881</doi></addata></record> |
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source | Open Access: PubMed Central; Publicly Available Content (ProQuest); Nature Journals Online; Springer Nature - nature.com Journals - Fully Open Access |
title | Poly(4-styrenesulfonate)-induced sulfur vacancy self-healing strategy for monolayer MoS 2 homojunction photodiode |
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