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Annual Meeting Optical Society of America

Optical spectroscopy using a solid as a single-molecule trap

W. E. Moerner, Th. Basché, Michel Orrit

Published Jan 1, 1992• 0 citations
Publisher

Abstract

As was recently demonstrated1 by using highly efficient fluorescence excitation spcctroscopy with N.A. = 0.98 collection optics, single impurity molecules in both crystals and polymers may now be detected with single-to-noiseratios (SNRs) as high as 30 in a 1 Hz bandwidth at low temperatures. In essence, the solid may be regarded as a trap for the single molecule, which effectively quenches rotation. Our measurements include precise determination of the lifetime limited linewidth and the temperature dependence of the optical dephasing, as well as spectral diffusion (wandering in frequency space due to perturbations by lattice degrees of freedom). For the polymeric host, light-induced changes in resonant frequency of a single molecule can be produced, a process that is normally termed spectral hole-burning when large ensembles of molecules are probed. In recent studies, nonclassical light emission from a single molecule (photon antibunching) has been observed in a fashion analogous to that reported earlier for a single atom in a trap.

DOI
10.1364/oam.1992.mtt2

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•May 8, 2019•4 citations
As was recently demonstrated1 by using highly efficient fluorescence excitation spcctroscopy with N.A. = 0.98 collection optics, single impurity molecules in both crystals and polymers may now be detected with single-to-noiseratios (SNRs) as high as 30 in a 1 Hz bandwidth at low temperatures. In essence, the solid may be regarded as a trap for the single molecule, which effectively quenches rotation. Our measurements include precise determination of the lifetime limited linewidth and the temperature dependence of the optical dephasing, as well as spectral diffusion (wandering in frequency space due to perturbations by lattice degrees of freedom). For the polymeric host, light-induced changes in resonant frequency of a single molecule can be produced, a process that is normally termed spectral hole-burning when large ensembles of molecules are probed. In recent studies, nonclassical light emission from a single molecule (photon antibunching) has been observed in a fashion analogous to that reported earlier for a single atom in a trap.
Recent advances in absorption1 and fluorescence2 detection now allow high-quality measurement of the optical absorption spectrum of individual single-impurity molecules in both crystals and polymers at liquid-helium temperatures. Here, the solid may be viewed as a trap for the defect center similar to the well-known electromagnetic single-ion traps, except that Doppler and recoil effects are replaced by (static) inhomogeneous broadening and host-guest interactions. Most importantly, molecular rotation is absent because of steric effects at low temperatures.
Single-molecule detection and spectroscopy in solids has the potential for direct observation of the microscopic physics and chemistry of defects without multicenter averaging. Initial observations of the optical absorption spectra of a single pentacene molecule in p-terphenyl crystals achieved signal-to-noise ratios (SNR's) of 3-5 in a 1-Hz bandwidth and required intensities at the sample above the saturation intensity. Careful noise analysis of our detectors showed that little improvement in SNR could be expected with an absorption technique unless simple and reliable sources of squeezed light were available. Recent advances in fluorescence- excitation spectroscopy have removed this SNR limitation.3
Experiments with single quantum systems are at the frontier of modern physics. Probing single molecules allows for very precise control of light-matter interaction and for quantum optical studies. Moreover, a single guest molecule in a solid host matrix is a very sensitive probe of local dynamics in its nano-environment. Fluorescence excitation spectroscopy on single molecules is a powerful tool for spectroscopic characterizations at highest resolution, as information can be revealed that is not accessible in experiments on ensembles of molecules. The detection of the fluorescence signal of a single absorber is achieved by exploiting the high spectral selectivity given by the ratio (10 10) of homogeneous to inhomogeneous linewidths of optical transitions at cryogenic temperatures (zero-phonon transitions). Two-photon fluorescence excitation, a fundamental nonlinear optical process, was observed on a single quantum system [1]. Single diphenyl-octatetraene molecules trapped in an n-tetradecane matrix were excited from the 1Ag ground to the lowest excited singlet state by simultaneous absorption of two photons using a single-mode cw laser. Excited molecules were observed through weak one-photon emission resulting from a symmetry breaking induced by the crystal field. The fundamental principles and the experimental technique of single molecule spectroscopy will be introduced briefly and some particular single molecule experiments presented. This work was done in collaboration with T. Plakhotnik, A. Renn and U.P. Wild
Abstract Optical spectroscopy of a single impurity molecule provides the first truly local probe of host–guest interactions in doped solids. In conventional optical high‐resolution experiments with many molecules only ensemble averages of the microscopic parameters can be obtained. In the single‐molecule regime, the exquisite sensitivity of an individual dopant molecule to both the local environment and to external perturbations has been exploited in recent experiments to reveal a wealth of fascinating novel phenomena such as spectral diffusion in crystals and polymers, optical modification of a single impurity molecule (spectral hole‐burning), local field measurements at the site of a single impurity molecule, and quantum optics in a solid.
Recent advances in the optical detection and spectroscopy of single impurity centers in crystals has provided the possibility of obtaining information about defect-solid interactions on a truly local level. For the system composed of pentacene impurity molecules in the crystal p-terphenyl, single molecules have been studied using both absorption1 and fluorescence excitation2 techniques at liquid helium temperatures. The superior signal-to-noise of the latter technique has led to direct observations of the lifetime-limited Lorentzian homogeneous profile of a single pentacene impurity3 as well as the surprising observation of spontaneous spectral diffusion4. Spectral diffusion, or changes in the resonance frequency of an impurity molecule with time as a result of low-energy excitations (two-level system transitions (TLS)),5 is generally expected in amorphous hosts. Indeed, the presence of TLSs in amorphous solids is intimately connected with nonphotochemical mechanisms for persistent spectral hole-burning (PSHB) in amorphous materials6-8. Using perylene impurity molecules in poly(ethylene), we have observed the optical spectra of single molecules in a polymeric host for the first time. At 1.5K, individual perylene molecules show the expected spectral diffusion; moreover, we observe light-induced changes in resonance frequency, i.e., persistent spectral hole-burning, which allows one to envision optical storage on the single-molecule level.
Optical spectroscopy of single impurity molecules in low-temperature solids provides an exquisitely sensitive probe of the structure and dynamics of the specific local environment around the single molecule, unobscured by ensemble averaging. Effects such as spectral diffusion, perturbations by external fields, changes in molecular photophysics, optical switching, dynamics due to amorphous system physics, magnetic resonance of a single molecular spin, and perturbations due to nearby charge transport have all been observed. Because properly chosen single molecules act as two- and three-level quantum systems, a variety of quantum optical effects may be observed, such as photon antibunching, optical Stark effect, and single-photon emission on command. When they carry spin in their ground and excited states, single molecules and other nano-objects open many more experiments in quantum optics and nanophysics, because they are sensitive to magnetic interactions and can serve as readouts for spin systems with long coherence times. As a new class of nanoscale experiments, the ability to optically pump and probe single 2–3-nm-sized molecules in complex systems provides a new window into the local dynamics and heterogeneity of solids.