{"title":"深紫外激发下二硫化钼范德华异质结构界面能量传递的光谱特征。","authors":"Tsung-Hsien Lee, Sheng-Lung Chou, Tzu-Ping Huang, Chak-Ming Liu, Chih-Hao Chin, Meng-Yeh Lin, Hui-Fen Chen and Yu-Jong Wu","doi":"10.1039/D5RA04686F","DOIUrl":null,"url":null,"abstract":"<p >We report a comprehensive photoluminescence (PL) and photoluminescence excitation (PLE) study of monolayer MoS<small><sub>2</sub></small> and its van der Waals heterostructures with hBN and graphene under deep-ultraviolet (DUV) excitation. Using synchrotron-based VUV/UV spectroscopy, we reveal that while pristine MoS<small><sub>2</sub></small> exhibits only A-exciton emission at ∼660 nm under visible excitation, broadband near-infrared emission (750–900 nm) emerges at cryogenic temperatures under DUV excitation in MoS<small><sub>2</sub></small>/hBN and MoS<small><sub>2</sub></small>/graphene heterostructures. This emission indicates a nonlocal excitation–emission mechanism facilitated by interfacial energy transfer from the UV-absorbing layers. In MoS<small><sub>2</sub></small>/hBN, a broad UV band near 350 nm also appears under 200 nm excitation and is attributed to impurity-related defect luminescence in hBN. The interfacial processes are governed by temperature-sensitive radiative channels involving defect-bound states or localized excitons in MoS<small><sub>2</sub></small>. Our results highlight the crucial role of interlayer coupling and spectral sensitization in enabling new radiative pathways in 2D heterostructures, offering novel strategies for tailoring light emission in layered optoelectronic systems.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 44","pages":" 37183-37193"},"PeriodicalIF":4.6000,"publicationDate":"2025-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12498572/pdf/","citationCount":"0","resultStr":"{\"title\":\"Spectroscopic signatures of interfacial energy transfer in MoS2-based van der Waals heterostructures under deep-UV excitation\",\"authors\":\"Tsung-Hsien Lee, Sheng-Lung Chou, Tzu-Ping Huang, Chak-Ming Liu, Chih-Hao Chin, Meng-Yeh Lin, Hui-Fen Chen and Yu-Jong Wu\",\"doi\":\"10.1039/D5RA04686F\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We report a comprehensive photoluminescence (PL) and photoluminescence excitation (PLE) study of monolayer MoS<small><sub>2</sub></small> and its van der Waals heterostructures with hBN and graphene under deep-ultraviolet (DUV) excitation. Using synchrotron-based VUV/UV spectroscopy, we reveal that while pristine MoS<small><sub>2</sub></small> exhibits only A-exciton emission at ∼660 nm under visible excitation, broadband near-infrared emission (750–900 nm) emerges at cryogenic temperatures under DUV excitation in MoS<small><sub>2</sub></small>/hBN and MoS<small><sub>2</sub></small>/graphene heterostructures. This emission indicates a nonlocal excitation–emission mechanism facilitated by interfacial energy transfer from the UV-absorbing layers. In MoS<small><sub>2</sub></small>/hBN, a broad UV band near 350 nm also appears under 200 nm excitation and is attributed to impurity-related defect luminescence in hBN. The interfacial processes are governed by temperature-sensitive radiative channels involving defect-bound states or localized excitons in MoS<small><sub>2</sub></small>. Our results highlight the crucial role of interlayer coupling and spectral sensitization in enabling new radiative pathways in 2D heterostructures, offering novel strategies for tailoring light emission in layered optoelectronic systems.</p>\",\"PeriodicalId\":102,\"journal\":{\"name\":\"RSC Advances\",\"volume\":\" 44\",\"pages\":\" 37183-37193\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-10-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12498572/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Advances\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra04686f\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra04686f","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Spectroscopic signatures of interfacial energy transfer in MoS2-based van der Waals heterostructures under deep-UV excitation
We report a comprehensive photoluminescence (PL) and photoluminescence excitation (PLE) study of monolayer MoS2 and its van der Waals heterostructures with hBN and graphene under deep-ultraviolet (DUV) excitation. Using synchrotron-based VUV/UV spectroscopy, we reveal that while pristine MoS2 exhibits only A-exciton emission at ∼660 nm under visible excitation, broadband near-infrared emission (750–900 nm) emerges at cryogenic temperatures under DUV excitation in MoS2/hBN and MoS2/graphene heterostructures. This emission indicates a nonlocal excitation–emission mechanism facilitated by interfacial energy transfer from the UV-absorbing layers. In MoS2/hBN, a broad UV band near 350 nm also appears under 200 nm excitation and is attributed to impurity-related defect luminescence in hBN. The interfacial processes are governed by temperature-sensitive radiative channels involving defect-bound states or localized excitons in MoS2. Our results highlight the crucial role of interlayer coupling and spectral sensitization in enabling new radiative pathways in 2D heterostructures, offering novel strategies for tailoring light emission in layered optoelectronic systems.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.