Observation of nanoscale opto-mechanical molecular damping as the origin of spectroscopic contrast in photo induced force microscopy.

Observation of nanoscale opto-mechanical molecular damping as the origin of spectroscopic contrast in photo induced force microscopy.
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DOI:
10.1038/s41467-020-19067-3
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发表时间:
2020-11-10
影响因子:
16.6
通讯作者:
Wickramasinghe HK
Wickramasinghe HK
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Almajhadi MA;Uddin SMA;Wickramasinghe HK

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Infrared photoinduced force microscopy (IR-PiFM) is a scanning probe spectroscopic technique that maps sample morphology and chemical properties on the nanometer (nm)-scale. Fabricated samples with nm periodicity such as self-assembly of block copolymer films can be chemically characterized by IR-PiFM with relative ease. Despite the success of IR-PiFM, the origin of spectroscopic contrast remains unclear, preventing the scientific community from conducting quantitative measurements. Here we experimentally investigate the contrast mechanism of IR-PiFM for recording vibrational resonances. We show that the measured spectroscopic information of a sample is directly related to the energy lost in the oscillating cantilever, which is a direct consequence of a molecule excited at its vibrational optical resonance—coined as opto-mechanical damping. The quality factor of the cantilever and the local sample polarizability can be mathematically correlated, enabling quantitative analysis. The basic theory for dissipative tip-sample interactions is introduced to model the observed opto-mechanical damping. Existing high-dimensional optical imaging techniques that record space and polarization cannot detect the photon’s time of arrival due to the limited speeds of electronic sensors. Here, the authors develop a single-shot ultrafast imaging modality to record light-speed high-dimensional events with picosecond resolution.
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