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The Role of Excitons and Free Charges in the Excited-State Dynamics of Solution-Processed Few-Layer MoS2 Nanoflakes
Solution-processed semiconducting transition metal dichalcogenides are emerging as promising two-dimensional materials for photovoltaic and optoelectronic applications. Here, we have used transient absorption spectroscopy to provide unambiguous evidence and distinct signatures of photogenerated exci...
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Published in: | Journal of physical chemistry. C 2016-10, Vol.120 (40), p.23286-23292 |
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container_end_page | 23292 |
container_issue | 40 |
container_start_page | 23286 |
container_title | Journal of physical chemistry. C |
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creator | Tsokkou, Demetra Yu, Xiaoyun Sivula, Kevin Banerji, Natalie |
description | Solution-processed semiconducting transition metal dichalcogenides are emerging as promising two-dimensional materials for photovoltaic and optoelectronic applications. Here, we have used transient absorption spectroscopy to provide unambiguous evidence and distinct signatures of photogenerated excitons and charges in solution-processed few-layer MoS2 nanoflakes (10–20 layers). We find that photoexcitation above the direct energy gap results in the ultrafast generation of a mixture of free charges in direct band states and of excitons. While the excitons are rapidly trapped, the free charges are long-lived with nanosecond recombination times. The different signatures observed for these species enable the experimental extraction of the exciton binding energy, which we find to be ∼80 meV in the nanoflakes, in agreement with reported values in the bulk material. Carrier-density-dependent measurements bring new insights about the many-body interactions between free charges resulting in band gap renormalization effects in the few-layer MoS2 nanoflakes. |
doi_str_mv | 10.1021/acs.jpcc.6b09267 |
format | article |
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Here, we have used transient absorption spectroscopy to provide unambiguous evidence and distinct signatures of photogenerated excitons and charges in solution-processed few-layer MoS2 nanoflakes (10–20 layers). We find that photoexcitation above the direct energy gap results in the ultrafast generation of a mixture of free charges in direct band states and of excitons. While the excitons are rapidly trapped, the free charges are long-lived with nanosecond recombination times. The different signatures observed for these species enable the experimental extraction of the exciton binding energy, which we find to be ∼80 meV in the nanoflakes, in agreement with reported values in the bulk material. Carrier-density-dependent measurements bring new insights about the many-body interactions between free charges resulting in band gap renormalization effects in the few-layer MoS2 nanoflakes.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.6b09267</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. 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C</addtitle><description>Solution-processed semiconducting transition metal dichalcogenides are emerging as promising two-dimensional materials for photovoltaic and optoelectronic applications. Here, we have used transient absorption spectroscopy to provide unambiguous evidence and distinct signatures of photogenerated excitons and charges in solution-processed few-layer MoS2 nanoflakes (10–20 layers). We find that photoexcitation above the direct energy gap results in the ultrafast generation of a mixture of free charges in direct band states and of excitons. While the excitons are rapidly trapped, the free charges are long-lived with nanosecond recombination times. The different signatures observed for these species enable the experimental extraction of the exciton binding energy, which we find to be ∼80 meV in the nanoflakes, in agreement with reported values in the bulk material. 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C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tsokkou, Demetra</au><au>Yu, Xiaoyun</au><au>Sivula, Kevin</au><au>Banerji, Natalie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Role of Excitons and Free Charges in the Excited-State Dynamics of Solution-Processed Few-Layer MoS2 Nanoflakes</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2016-10-13</date><risdate>2016</risdate><volume>120</volume><issue>40</issue><spage>23286</spage><epage>23292</epage><pages>23286-23292</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Solution-processed semiconducting transition metal dichalcogenides are emerging as promising two-dimensional materials for photovoltaic and optoelectronic applications. Here, we have used transient absorption spectroscopy to provide unambiguous evidence and distinct signatures of photogenerated excitons and charges in solution-processed few-layer MoS2 nanoflakes (10–20 layers). We find that photoexcitation above the direct energy gap results in the ultrafast generation of a mixture of free charges in direct band states and of excitons. While the excitons are rapidly trapped, the free charges are long-lived with nanosecond recombination times. The different signatures observed for these species enable the experimental extraction of the exciton binding energy, which we find to be ∼80 meV in the nanoflakes, in agreement with reported values in the bulk material. Carrier-density-dependent measurements bring new insights about the many-body interactions between free charges resulting in band gap renormalization effects in the few-layer MoS2 nanoflakes.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcc.6b09267</doi><tpages>7</tpages></addata></record> |
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title | The Role of Excitons and Free Charges in the Excited-State Dynamics of Solution-Processed Few-Layer MoS2 Nanoflakes |
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