MoS2 pixel arrays for real-time photoluminescence imaging of redox molecules
An array of micrometer-scale pixels of MoS 2 works as a fluorescent “redox screen” to visualize redox molecule concentration. Measuring the behavior of redox-active molecules in space and time is crucial for understanding chemical and biological systems and for developing new technologies. Optical s...
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Veröffentlicht in: | Science advances 2019-11, Vol.5 (11), p.eaat9476-eaat9476 |
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creator | Reynolds, M F Guimarães, M H D Gao, H Kang, K Cortese, A J Ralph, D C Park, J McEuen, P L |
description | An array of micrometer-scale pixels of MoS
2
works as a fluorescent “redox screen” to visualize redox molecule concentration.
Measuring the behavior of redox-active molecules in space and time is crucial for understanding chemical and biological systems and for developing new technologies. Optical schemes are noninvasive and scalable, but usually have a slow response compared to electrical detection methods. Furthermore, many fluorescent molecules for redox detection degrade in brightness over long exposure times. Here, we show that the photoluminescence of “pixel” arrays of monolayer MoS
2
can image spatial and temporal changes in redox molecule concentration. Because of the strong dependence of MoS
2
photoluminescence on doping, changes in the local chemical potential substantially modulate the photoluminescence of MoS
2
, with a sensitivity of 0.9
mV
/
Hz
on a 5 μm × 5 μm pixel, corresponding to better than parts-per-hundred changes in redox molecule concentration down to nanomolar concentrations at 100-ms frame rates. This provides a new strategy for visualizing chemical reactions and biomolecules with a two-dimensional material screen. |
doi_str_mv | 10.1126/sciadv.aat9476 |
format | Article |
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2
works as a fluorescent “redox screen” to visualize redox molecule concentration.
Measuring the behavior of redox-active molecules in space and time is crucial for understanding chemical and biological systems and for developing new technologies. Optical schemes are noninvasive and scalable, but usually have a slow response compared to electrical detection methods. Furthermore, many fluorescent molecules for redox detection degrade in brightness over long exposure times. Here, we show that the photoluminescence of “pixel” arrays of monolayer MoS
2
can image spatial and temporal changes in redox molecule concentration. Because of the strong dependence of MoS
2
photoluminescence on doping, changes in the local chemical potential substantially modulate the photoluminescence of MoS
2
, with a sensitivity of 0.9
mV
/
Hz
on a 5 μm × 5 μm pixel, corresponding to better than parts-per-hundred changes in redox molecule concentration down to nanomolar concentrations at 100-ms frame rates. This provides a new strategy for visualizing chemical reactions and biomolecules with a two-dimensional material screen.</description><identifier>EISSN: 2375-2548</identifier><identifier>DOI: 10.1126/sciadv.aat9476</identifier><identifier>PMID: 31723596</identifier><language>eng</language><publisher>American Association for the Advancement of Science</publisher><subject>Chemistry ; SciAdv r-articles</subject><ispartof>Science advances, 2019-11, Vol.5 (11), p.eaat9476-eaat9476</ispartof><rights>Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). 2019 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839941/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839941/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,53790,53792</link.rule.ids></links><search><creatorcontrib>Reynolds, M F</creatorcontrib><creatorcontrib>Guimarães, M H D</creatorcontrib><creatorcontrib>Gao, H</creatorcontrib><creatorcontrib>Kang, K</creatorcontrib><creatorcontrib>Cortese, A J</creatorcontrib><creatorcontrib>Ralph, D C</creatorcontrib><creatorcontrib>Park, J</creatorcontrib><creatorcontrib>McEuen, P L</creatorcontrib><title>MoS2 pixel arrays for real-time photoluminescence imaging of redox molecules</title><title>Science advances</title><description>An array of micrometer-scale pixels of MoS
2
works as a fluorescent “redox screen” to visualize redox molecule concentration.
Measuring the behavior of redox-active molecules in space and time is crucial for understanding chemical and biological systems and for developing new technologies. Optical schemes are noninvasive and scalable, but usually have a slow response compared to electrical detection methods. Furthermore, many fluorescent molecules for redox detection degrade in brightness over long exposure times. Here, we show that the photoluminescence of “pixel” arrays of monolayer MoS
2
can image spatial and temporal changes in redox molecule concentration. Because of the strong dependence of MoS
2
photoluminescence on doping, changes in the local chemical potential substantially modulate the photoluminescence of MoS
2
, with a sensitivity of 0.9
mV
/
Hz
on a 5 μm × 5 μm pixel, corresponding to better than parts-per-hundred changes in redox molecule concentration down to nanomolar concentrations at 100-ms frame rates. This provides a new strategy for visualizing chemical reactions and biomolecules with a two-dimensional material screen.</description><subject>Chemistry</subject><subject>SciAdv r-articles</subject><issn>2375-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVjztPwzAYRS0kRFHpyuyRJcXv2AsSQrykIgZgjhznS2vkxMFOqvbfE4kuTHe4V0fnInRNyZpSpm6z87bZr60djSjVGbpkvJQFk0Iv0Crnb0IIFUpJai7QgtOScWnUJdq8xQ-GB3-AgG1K9phxGxNOYEMx-g7wsItjDFPne8gOegfYd3br-y2O7Txr4gF3MYCbAuQrdN7akGF1yiX6enr8fHgpNu_Prw_3m2Jggo-Fm81k2daU1YoorSmoWkupwFrTMk1o3baqIaLWUBvmiKCuKUtuGietUqXkS3T3xx2muoNm1hqTDdWQZrV0rKL11f-m97tqG_eV0twYQWfAzQmQ4s8Eeaw6P78LwfYQp1wxToWUUhPDfwF5-Wrr</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Reynolds, M F</creator><creator>Guimarães, M H D</creator><creator>Gao, H</creator><creator>Kang, K</creator><creator>Cortese, A J</creator><creator>Ralph, D C</creator><creator>Park, J</creator><creator>McEuen, P L</creator><general>American Association for the Advancement of Science</general><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20191101</creationdate><title>MoS2 pixel arrays for real-time photoluminescence imaging of redox molecules</title><author>Reynolds, M F ; Guimarães, M H D ; Gao, H ; Kang, K ; Cortese, A J ; Ralph, D C ; Park, J ; McEuen, P L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p243t-c37557fb12b606881e6b8556eaa9f2801bff6d04b8eb92c041cd7739dc5a66753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Chemistry</topic><topic>SciAdv r-articles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reynolds, M F</creatorcontrib><creatorcontrib>Guimarães, M H D</creatorcontrib><creatorcontrib>Gao, H</creatorcontrib><creatorcontrib>Kang, K</creatorcontrib><creatorcontrib>Cortese, A J</creatorcontrib><creatorcontrib>Ralph, D C</creatorcontrib><creatorcontrib>Park, J</creatorcontrib><creatorcontrib>McEuen, P L</creatorcontrib><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Science advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reynolds, M F</au><au>Guimarães, M H D</au><au>Gao, H</au><au>Kang, K</au><au>Cortese, A J</au><au>Ralph, D C</au><au>Park, J</au><au>McEuen, P L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MoS2 pixel arrays for real-time photoluminescence imaging of redox molecules</atitle><jtitle>Science advances</jtitle><date>2019-11-01</date><risdate>2019</risdate><volume>5</volume><issue>11</issue><spage>eaat9476</spage><epage>eaat9476</epage><pages>eaat9476-eaat9476</pages><eissn>2375-2548</eissn><abstract>An array of micrometer-scale pixels of MoS
2
works as a fluorescent “redox screen” to visualize redox molecule concentration.
Measuring the behavior of redox-active molecules in space and time is crucial for understanding chemical and biological systems and for developing new technologies. Optical schemes are noninvasive and scalable, but usually have a slow response compared to electrical detection methods. Furthermore, many fluorescent molecules for redox detection degrade in brightness over long exposure times. Here, we show that the photoluminescence of “pixel” arrays of monolayer MoS
2
can image spatial and temporal changes in redox molecule concentration. Because of the strong dependence of MoS
2
photoluminescence on doping, changes in the local chemical potential substantially modulate the photoluminescence of MoS
2
, with a sensitivity of 0.9
mV
/
Hz
on a 5 μm × 5 μm pixel, corresponding to better than parts-per-hundred changes in redox molecule concentration down to nanomolar concentrations at 100-ms frame rates. This provides a new strategy for visualizing chemical reactions and biomolecules with a two-dimensional material screen.</abstract><pub>American Association for the Advancement of Science</pub><pmid>31723596</pmid><doi>10.1126/sciadv.aat9476</doi><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Chemistry SciAdv r-articles |
title | MoS2 pixel arrays for real-time photoluminescence imaging of redox molecules |
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