飞秒
傅里叶变换红外光谱
材料科学
光热治疗
红外线的
光学
傅里叶变换光谱学
显微镜
红外光谱学
傅里叶变换
红外显微镜
吸收(声学)
光电子学
分析化学(期刊)
化学
激光器
纳米技术
物理
有机化学
量子力学
色谱法
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-11-11
卷期号:22 (22): 9174-9180
被引量:8
标识
DOI:10.1021/acs.nanolett.2c04097
摘要
The mechanical detection of photothermal expansion from infrared (IR) absorption with an atomic force microscope (AFM) bypasses Abbe's diffraction limit, forming the chemical imaging technique of AFM-IR. Here, we develop a Fourier transform AFM-IR technique with peak force infrared microscopy and broadband femtosecond IR pulses. A Michelson interferometer creates a pair of IR pulses with controlled time delays to generate photothermal signals transduced by AFM to form an interferogram. A Fourier transform is performed to recover IR absorption spectra. We demonstrate the Fourier transform AFM-IR microscopy on a polymer blend and hexagonal boron nitride. An intriguing observation is the vertical asymmetry of the interferogram, which suggests the presence of multiphoton absorption processes under the tip-enhancement and femtosecond IR lasers. Our method demonstrates the feasibility of time-domain detection of the AFM-IR signal in the mid-IR regime and paves the way toward multiphoton vibrational spectroscopy at the nanoscale below the diffraction limit.
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