TY - JOUR
T1 - On-Chip Lock-In Detection for Ultrafast Spectroscopy of Single Particles
AU - Adhikari, Subhasis
AU - Gross, Niklas
AU - Wilson, Kelly S.
AU - Verma, Ojasvi
AU - Jia, Zhenyang
AU - Landes, Christy F.
AU - Roberts, Sean T.
AU - Link, Stephan
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/5/30
Y1 - 2024/5/30
N2 - Time-resolved spectroscopy of plasmonic nanoparticles is a vital technique for probing their ultrafast electron dynamics and subsequent acoustic and photothermal properties. Traditionally, these experiments are performed with spectrally broad probe beams on the ensemble level to achieve high signal amplitudes. However, the relaxation dynamics of plasmonic nanoparticles is highly dependent on their size, shape, and crystallinity. As such, the inherent heterogeneity of most nanoparticle samples can complicate efforts to build microscopic models for these dynamics solely on the basis of ensemble measurements. Although approaches for collecting time-resolved microscopy signals from individual nanoparticles at selected probe wavelengths have been demonstrated, acquiring time-resolved spectra from single objects remains challenging. Here, we demonstrate an alternate method that efficiently yields the time-resolved spectra of a single gold nanodisk in one measurement. By modulating the frequency-doubled output of a 96 MHz Ti:sapphire oscillator at 8 kHz, we are able to use a lock-in pixel-array camera to detect photoinduced changes in the transmission of a white light continuum probe derived from a photonic crystal fiber to produce broadband femtosecond transmission spectra of a single gold nanodisk. We also compare the performance of the lock-in camera for the same single nanoparticle to measurements with a single-element photodiode and find comparable sensitivities. The lock-in camera thus provides a major advantage due to its ability to multiplex spectral detection, which we utilize here to capture both the electronic dynamics and acoustic vibrations of a single gold nanodisk following ultrafast laser excitation.
AB - Time-resolved spectroscopy of plasmonic nanoparticles is a vital technique for probing their ultrafast electron dynamics and subsequent acoustic and photothermal properties. Traditionally, these experiments are performed with spectrally broad probe beams on the ensemble level to achieve high signal amplitudes. However, the relaxation dynamics of plasmonic nanoparticles is highly dependent on their size, shape, and crystallinity. As such, the inherent heterogeneity of most nanoparticle samples can complicate efforts to build microscopic models for these dynamics solely on the basis of ensemble measurements. Although approaches for collecting time-resolved microscopy signals from individual nanoparticles at selected probe wavelengths have been demonstrated, acquiring time-resolved spectra from single objects remains challenging. Here, we demonstrate an alternate method that efficiently yields the time-resolved spectra of a single gold nanodisk in one measurement. By modulating the frequency-doubled output of a 96 MHz Ti:sapphire oscillator at 8 kHz, we are able to use a lock-in pixel-array camera to detect photoinduced changes in the transmission of a white light continuum probe derived from a photonic crystal fiber to produce broadband femtosecond transmission spectra of a single gold nanodisk. We also compare the performance of the lock-in camera for the same single nanoparticle to measurements with a single-element photodiode and find comparable sensitivities. The lock-in camera thus provides a major advantage due to its ability to multiplex spectral detection, which we utilize here to capture both the electronic dynamics and acoustic vibrations of a single gold nanodisk following ultrafast laser excitation.
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U2 - 10.1021/acs.jpcc.4c01814
DO - 10.1021/acs.jpcc.4c01814
M3 - Article
AN - SCOPUS:85193508044
SN - 1932-7447
VL - 128
SP - 8708
EP - 8715
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 21
ER -