Broadband single-molecule excitation spectroscopy
نویسندگان
چکیده
Over the past 25 years, single-molecule spectroscopy has developed into a widely used tool in multiple disciplines of science. The diversity of routinely recorded emission spectra does underpin the strength of the single-molecule approach in resolving the heterogeneity and dynamics, otherwise hidden in the ensemble. In early cryogenic studies single molecules were identified by their distinct excitation spectra, yet measuring excitation spectra at room temperature remains challenging. Here we present a broadband Fourier approach that allows rapid recording of excitation spectra of individual molecules under ambient conditions and that is robust against blinking and bleaching. Applying the method we show that the excitation spectra of individual molecules exhibit an extreme distribution of solvatochromic shifts and distinct spectral shapes. Importantly, we demonstrate that the sensitivity and speed of the broadband technique is comparable to that of emission spectroscopy putting both techniques side-by-side in single-molecule spectroscopy.
منابع مشابه
Vibrationally-Mediated Dynamics in β-carotene Probed with Broadband 2D Electronic Spectroscopy
Competing electronic pathways exhibiting energy dependence across a single vibronic excitation are observed in β-carotene for the first time with broadband two-dimensional electronic spectroscopy at 77K. The origins and implications of these features are discussed.
متن کاملMulticolour single molecule emission and excitation spectroscopy reveals extensive spectral shifts.
We explore the distribution and shape of single molecule spectra at room temperature, when embedded in a polymer host. Multicolour excitation and emission spectroscopy is implemented to capture the full inhomogeneous distribution. We observe dramatic spectral changes in a distribution of single quaterrylene diimide (QDI) molecules isolated in a PMMA matrix. The molecules are strongly blue shift...
متن کاملSurface-enhanced Raman excitation spectroscopy of a single rhodamine 6G molecule.
The surface-enhanced Raman excitation profiles (REPs) of rhodamine 6G (R6G) on Ag surfaces are studied using a tunable optical parametric oscillator excitation source and versatile detection scheme. These experiments afford the ability to finely tune the excitation wavelength near the molecular resonance of R6G (i.e., approximately 500-575 nm) and perform wavelength-scanned surface-enhanced Ram...
متن کاملThermometry for turbulent flames by coherent anti-Stokes Raman spectroscopy with simultaneous referencing to the modeless excitation profile.
An optimal system for temperature measurements by coherent anti-Stokes Raman spectroscopy (CARS) in turbulent flames and flows is presented. In addition to a single-mode pump laser and a modeless dye laser, an echelle spectrometer with a cross disperser is used. This system permits simultaneous measurement of the N2 CARS spectrum and the broadband dye laser profile. A procedure is developed to ...
متن کاملPushing the Sample-Size Limit of Infrared Vibrational Nanospectroscopy: From Monolayer toward Single Molecule Sensitivity.
While scattering-scanning near-field optical microscopy (s-SNOM) has demonstrated its potential to extend infrared (IR) spectroscopy into the nanometer scale, it has not yet reached its full potential in terms of spectroscopic sensitivity. We combine broadband femtosecond mid-IR excitation with an optimized spectral irradiance of ∼2 W/cm(2)/ cm(-1) (power/area/bandwidth) and a combination of ti...
متن کامل