Excitation Laser Energy Dependence of the Gap-Mode TERS Spectra of WS2 and MoS2 on Silver

被引:0
作者
Krayev, Andrey [1 ]
Isotta, Eleonora [2 ]
Hoang, Lauren [3 ]
Yang, Jerry A. [3 ]
Neilson, Kathryn [3 ]
Wang, Minyuan [4 ]
Haughn, Noah [4 ]
Pop, Eric [3 ,5 ]
Mannix, Andrew [5 ]
Balogun, Oluwaseyi [6 ,7 ]
Wang, Chih-Feng [8 ]
机构
[1] HORIBA Sci, Novato, CA 94949 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[4] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[5] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[6] Northwestern Univ, Dept Mech Engn, Evanston, IL 60208 USA
[7] Northwestern Univ, Dept Civil & Environm Engn, Evanston, IL 60208 USA
[8] Pacific Northwest Natl Lab, Richland, WA 99352 USA
来源
ACS PHOTONICS | 2025年 / 12卷 / 03期
基金
美国国家科学基金会; 美国能源部;
关键词
tip-enhanced Raman spectroscopy; excitationenergy dependence; transition metal dichalcogenides; concurrent excitationand collection; nanocavity plasmon and TMD exciton coupling; TRANSITION-METAL DICHALCOGENIDES; MONOLAYER; NANOROD; PROBE;
D O I
10.1021/acsphotonics.4c02257
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, we present a systematic study of the dependence of the gap-mode tip-enhanced Raman scattering (TERS) response of the mono- and bilayer WS2 and MoS2 on silver as a function of the excitation laser energy in a broad spectral range from 473 to 830 nm. For this purpose, we collected consecutive TERS maps of the same area in the sample containing mono- and bilayer regions with the same TERS probe with 6 different excitation lasers. To decrease the number of collected TERS maps, we used for the first time, to the best of our knowledge, concurrent excitation and collection with two lasers simultaneously. We found that the E2g/A1g peak intensity ratio for the bilayer WS2@Ag and the ratio of the A '/A1g peak intensity of the out-of-plane mode for the mono- and the bilayer change in a significantly nonmonotonous way as the excitation laser energy is swept from 1.58 to 2.62 eV. The former ratio increases at energies corresponding to A and B excitons (similar to 2.0 and 2.4 eV, respectively) in bilayer WS2. The absolute intensity of the A ' peak in the monolayer, and correspondingly the A '/A1g ratio, is surprisingly high at lower excitation energies but dips dramatically at the energy corresponding to the A exciton, being restored partially in between A and B excitons, but still showing the descending trend as the excitation laser energy increases. A somewhat similar picture was observed in mono- and bilayers of MoS2@Ag, though the existing set of excitation lasers did not match the excitonic profile of this material as nicely as for the case of WS2. We attribute the observed behavior to the presence of intermediate (Fano resonance) or strong (Rabi splitting) coupling between the excitons in transition metal dichalcogenides (TMDs) and the plasmons in the tip-substrate nanocavity. This is akin to the so-called "Fano" (Rabi) transparency experimentally observed in far-field scattering from TMDs between two plasmonic metals. The possibility of the formation of intermediate/strong coupling between the excitonic resonances in TMDs and the nanocavity reevaluates the role of various resonances in gap-mode TERS, and should become an important factor to be considered by TERS practitioners during experiment planning. Finally, based on the observed phenomena and their explanation, we propose the "ideal" substrate for efficient TERS and tip-enhanced photoluminescence (TEPL) measurements.
引用
收藏
页码:1535 / 1544
页数:10
相关论文
共 50 条
  • [21] Intermixing of MoS2 and WS2 photocatalysts toward methylene blue photodegradation
    Al Qaydi, Maryam
    Rajput, Nitul S.
    Lejeune, Michael
    Bouchalkha, Abdellatif
    El Marssi, Mimoun
    Cordette, Steevy
    Kasmi, Chaouki
    Jouiad, Mustapha
    BEILSTEIN JOURNAL OF NANOTECHNOLOGY, 2024, 15 : 817 - 829
  • [22] Two-dimensional WS2/MoS2 heterostructures: properties and applications
    Chen, Yichuan
    Sun, Mengtao
    NANOSCALE, 2021, 13 (11) : 5594 - 5619
  • [23] Origin of Indirect Optical Transitions in Few-Layer MoS2, WS2, and WSe2
    Zhao, Weijie
    Ribeiro, R. M.
    Toh, Minglin
    Carvalho, Alexandra
    Kloc, Christian
    Castro Neto, A. H.
    Eda, Goki
    NANO LETTERS, 2013, 13 (11) : 5627 - 5634
  • [24] Modeling the coverage of MoS2 and WS2 thin films using in-situ spectroscopic ellipsometry
    Houser, Elizabeth
    Knight, Thomas V. Mc
    Redwing, Joan M.
    Peiris, Frank C.
    JOURNAL OF CRYSTAL GROWTH, 2024, 640
  • [25] Phonon scattering mechanism in van der Waals heterostructures comprising of MoS2 and WS2 nanosheets
    Sinha, Sneha
    Arora, Sunil K.
    Wu, Han-Chun
    Sathe, Vasant G.
    MATERIALS TODAY-PROCEEDINGS, 2021, 45 : 4612 - 4618
  • [26] Imaging of Defect-Accelerated Energy Transfer in MoS2/hBN/WS2 Heterostructures
    Wang, Jiangcai
    Liu, Huan
    Hu, Xiangmin
    Liu, Yuanshuang
    Liu, Dameng
    ACS APPLIED MATERIALS & INTERFACES, 2022, 14 (06) : 8521 - 8526
  • [27] Temperature dependent Raman and photoluminescence of vertical WS2/MoS2 monolayer heterostructures
    Hu, Zhijian
    Bao, Yanjun
    Li, Ziwei
    Gong, Yongji
    Feng, Rui
    Xiao, Yingdong
    Wu, Xiaochun
    Zhang, Zhaohui
    Zhu, Xing
    Ajayan, Pulickel M.
    Fang, Zheyu
    SCIENCE BULLETIN, 2017, 62 (01) : 16 - 21
  • [28] Decoration of WS2 Nanotubes and Fullerene-Like MoS2 with Gold Nanoparticles
    Polyakov, Alexander Yu.
    Yadgarov, Lena
    Popovitz-Biro, Ronit
    Lebedev, Vasily A.
    Pinkas, Iddo
    Rosentsveig, Rita
    Feldman, Yishay
    Goldt, Anastasia E.
    Goodilin, Eugene A.
    Tenne, Reshef
    JOURNAL OF PHYSICAL CHEMISTRY C, 2014, 118 (04) : 2161 - 2169
  • [29] Tuning Carrier Confinement in the MoS2/WS2 Lateral Heterostructure
    Kang, Jun
    Sahin, Hasan
    Peeters, Francois M.
    JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (17) : 9580 - 9586
  • [30] Determining the thickness of atomically thin MoS2 and WS2 in the TEM
    Wu, Ryan J.
    Odlyzko, Michael L.
    Mkhoyan, K. Andre
    ULTRAMICROSCOPY, 2014, 147 : 8 - 20