Lei Chen, Juan Pedro Merino, Miquel Torrent-Sucarrat, Hui-Lei Hou, Maurizio Prato
{"title":"电荷转移诱导的 SERS 增强取决于 MoS2 掺杂剂的相互作用差异","authors":"Lei Chen, Juan Pedro Merino, Miquel Torrent-Sucarrat, Hui-Lei Hou, Maurizio Prato","doi":"10.1002/admi.202400272","DOIUrl":null,"url":null,"abstract":"<p>2D transition metal dichalcogenide materials have attracted increasing attention as active surface-enhanced Raman spectroscopy (SERS) platforms. In this study, the influence of n- and p-type doping of exfoliated MoS<sub>2</sub> (exMoS<sub>2</sub>) hybrids on the SERS performance is investigated, employing Rhodamine 6G (R6G) as a probe molecule. It is demonstrated that n-doped exMoS<sub>2</sub> hybrids (exMoS<sub>2</sub> mixed with C<sub>60</sub>, graphene, and sodium dodecyl sulfate) exhibit enhanced SERS intensities, while p-doping (exMoS<sub>2</sub> mixed with TCNQ) resulted in inhibited SERS enhancement. A key discovery is the linear relationship between Raman enhancement of MoS<sub>2</sub>/dopant hybrids and the difference in their LUMO energy levels, which dictate the degree and direction of charge transfer. Interestingly, MC<sub>60</sub>-4, a C<sub>60</sub>-doped hybrid, deviates from the linear relationship, displaying remarkable SERS enhancement owing to its chemical interaction and unique Raman scattering activity. The findings provide critical insights into the SERS enhancement behavior of doped MoS<sub>2</sub>, facilitating precise tuning of SERS intensities by manipulating the MoS<sub>2</sub> doping state.</p>","PeriodicalId":115,"journal":{"name":"Advanced Materials Interfaces","volume":"11 28","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admi.202400272","citationCount":"0","resultStr":"{\"title\":\"Charge Transfer-Induced SERS Enhancement of MoS2/Dopants Dependent on their Interaction Difference\",\"authors\":\"Lei Chen, Juan Pedro Merino, Miquel Torrent-Sucarrat, Hui-Lei Hou, Maurizio Prato\",\"doi\":\"10.1002/admi.202400272\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>2D transition metal dichalcogenide materials have attracted increasing attention as active surface-enhanced Raman spectroscopy (SERS) platforms. In this study, the influence of n- and p-type doping of exfoliated MoS<sub>2</sub> (exMoS<sub>2</sub>) hybrids on the SERS performance is investigated, employing Rhodamine 6G (R6G) as a probe molecule. It is demonstrated that n-doped exMoS<sub>2</sub> hybrids (exMoS<sub>2</sub> mixed with C<sub>60</sub>, graphene, and sodium dodecyl sulfate) exhibit enhanced SERS intensities, while p-doping (exMoS<sub>2</sub> mixed with TCNQ) resulted in inhibited SERS enhancement. A key discovery is the linear relationship between Raman enhancement of MoS<sub>2</sub>/dopant hybrids and the difference in their LUMO energy levels, which dictate the degree and direction of charge transfer. Interestingly, MC<sub>60</sub>-4, a C<sub>60</sub>-doped hybrid, deviates from the linear relationship, displaying remarkable SERS enhancement owing to its chemical interaction and unique Raman scattering activity. The findings provide critical insights into the SERS enhancement behavior of doped MoS<sub>2</sub>, facilitating precise tuning of SERS intensities by manipulating the MoS<sub>2</sub> doping state.</p>\",\"PeriodicalId\":115,\"journal\":{\"name\":\"Advanced Materials Interfaces\",\"volume\":\"11 28\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-08-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/admi.202400272\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Materials Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/admi.202400272\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Materials Interfaces","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/admi.202400272","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Charge Transfer-Induced SERS Enhancement of MoS2/Dopants Dependent on their Interaction Difference
2D transition metal dichalcogenide materials have attracted increasing attention as active surface-enhanced Raman spectroscopy (SERS) platforms. In this study, the influence of n- and p-type doping of exfoliated MoS2 (exMoS2) hybrids on the SERS performance is investigated, employing Rhodamine 6G (R6G) as a probe molecule. It is demonstrated that n-doped exMoS2 hybrids (exMoS2 mixed with C60, graphene, and sodium dodecyl sulfate) exhibit enhanced SERS intensities, while p-doping (exMoS2 mixed with TCNQ) resulted in inhibited SERS enhancement. A key discovery is the linear relationship between Raman enhancement of MoS2/dopant hybrids and the difference in their LUMO energy levels, which dictate the degree and direction of charge transfer. Interestingly, MC60-4, a C60-doped hybrid, deviates from the linear relationship, displaying remarkable SERS enhancement owing to its chemical interaction and unique Raman scattering activity. The findings provide critical insights into the SERS enhancement behavior of doped MoS2, facilitating precise tuning of SERS intensities by manipulating the MoS2 doping state.
期刊介绍:
Advanced Materials Interfaces publishes top-level research on interface technologies and effects. Considering any interface formed between solids, liquids, and gases, the journal ensures an interdisciplinary blend of physics, chemistry, materials science, and life sciences. Advanced Materials Interfaces was launched in 2014 and received an Impact Factor of 4.834 in 2018.
The scope of Advanced Materials Interfaces is dedicated to interfaces and surfaces that play an essential role in virtually all materials and devices. Physics, chemistry, materials science and life sciences blend to encourage new, cross-pollinating ideas, which will drive forward our understanding of the processes at the interface.
Advanced Materials Interfaces covers all topics in interface-related research:
Oil / water separation,
Applications of nanostructured materials,
2D materials and heterostructures,
Surfaces and interfaces in organic electronic devices,
Catalysis and membranes,
Self-assembly and nanopatterned surfaces,
Composite and coating materials,
Biointerfaces for technical and medical applications.
Advanced Materials Interfaces provides a forum for topics on surface and interface science with a wide choice of formats: Reviews, Full Papers, and Communications, as well as Progress Reports and Research News.