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Applied Physics Reviews

Photon correlations probe the quantized nature of light emission from optoelectronic materials

John M. Lupton, Jan Vogelsang

Published Oct 1, 2021• 14 citations
Publisher

Abstract

Even though the quantized interaction between light and matter in the photoelectric effect is considered one of the cornerstones in the development of quantum mechanics, it was long thought impossible to directly observe the quantized nature of light itself. The advent of light-intensity autocorrelation techniques in the 1950s, first developed to study the size of stars, changed little in this perception, until true single-photon correlation spectroscopy from trapped ions was proven to be possible in the late 1970s: Photons from a single quantum emitter tend to arrive in bunches, but each light quantum is spaced apart in time—it is antibunched. Initially considered only as the workhorse of atomic quantum optics, over the past two decades, photon correlation techniques have become a standard in fields as diverse as quantum-information processing, biological imaging, polymer physics, and materials science, in general. The technique is particularly useful for probing materials that are specifically designed to emit or absorb light in optoelectronic devices, such as light-emitting diodes, solar cells, or lasers. The central question in such studies is how large a mesoscopic piece of material can become and still behave as an atom-like source of single photons. What interactions may arise between multiple excitations within a material, and what sort of dark states may give rise to intermittency in the stream of photons? We review the many different classes of optoelectronic materials for which photon-correlation spectroscopy has proven to offer useful insight into excited-state dynamics, ranging from molecular, over semiconductor to metallic nanostructures. The technique is particularly suited to probing mesoscopic aggregates of organic semiconductors since each single molecule acts as a quantum emitter itself.

DOI
10.1063/5.0059764

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Even though the quantized interaction between light and matter in the photoelectric effect is considered one of the cornerstones in the development of quantum mechanics, it was long thought impossible to directly observe the quantized nature of light itself. The advent of light-intensity autocorrelation techniques in the 1950s, first developed to study the size of stars, changed little in this perception, until true single-photon correlation spectroscopy from trapped ions was proven to be possible in the late 1970s: Photons from a single quantum emitter tend to arrive in bunches, but each light quantum is spaced apart in time—it is antibunched. Initially considered only as the workhorse of atomic quantum optics, over the past two decades, photon correlation techniques have become a standard in fields as diverse as quantum-information processing, biological imaging, polymer physics, and materials science, in general. The technique is particularly useful for probing materials that are specifically designed to emit or absorb light in optoelectronic devices, such as light-emitting diodes, solar cells, or lasers. The central question in such studies is how large a mesoscopic piece of material can become and still behave as an atom-like source of single photons. What interactions may arise between multiple excitations within a material, and what sort of dark states may give rise to intermittency in the stream of photons? We review the many different classes of optoelectronic materials for which photon-correlation spectroscopy has proven to offer useful insight into excited-state dynamics, ranging from molecular, over semiconductor to metallic nanostructures. The technique is particularly suited to probing mesoscopic aggregates of organic semiconductors since each single molecule acts as a quantum emitter itself.
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The interaction of light with nanometer-sized structures is at the core of nano-optics. It is obvious that as the particles become smaller and smaller the laws of quantum mechanics will become apparent in their interaction with light. In this limit, continuous scattering and absorption of light will be supplemented or replaced by resonant interactions if the photon energy hits the energy difference of discrete internal (electronic) energy levels. In atoms, molecules and nanoparticles, like semiconductor nanocrystals and other “quantum confined” systems, these resonances are found at optical frequencies. Due to the resonant character, the light–matter interaction can often be approximated by treating the quantum system as an effective two-level system, i.e. by considering only those two (electronic) levels whose difference in energy is close to the interacting photon energy ħ ω 0 . In this chapter we consider single-quantum systems that are fixed in space, either by deposition to a surface or by being embedded into a solid matrix. The material to be covered should familiarize the reader with single-photon emitters and with concepts developed in the field of quantum optics. While various theoretical aspects related to the fields emitted by a quantum system have been discussed in Chapter 8, the current chapter focuses more on the nature of the quantum system itself. We adopt a rather practical perspective since more rigorous accounts can be found elsewhere (see e.g. [1–4]).
The concept of the photon , central to Einstein's explanation of the photoelectric effect, is exactly 100 years old. Yet, while photons have been detected individually for more than 50 years, devices producing individual photons on demand have only appeared in the last few years. New concepts for single-photon sources, or 'photon guns', have originated from recent progress in the optical detection, characterization and manipulation of single quantum objects. Single emitters usually deliver photons one at a time. This so-called antibunching of emitted photons can arise from various mechanisms, but ensures that the probability of obtaining two or more photons at the same time remains negligible. We briefly recall basic concepts in quantum optics and discuss potential applications of single-photon states to optical processing of quantum information: cryptography, computing and communication. A photon gun's properties are significantly improved by coupling it to a resonant cavity mode, either in the Purcell or strong-coupling regimes. We briefly recall early production of single photons with atomic beams, and the operation principles of macroscopic parametric sources, which are used in an overwhelming majority of quantum-optical experiments. We then review the photophysical and spectroscopic properties and compare the advantages and weaknesses of various single nanometre-scale objects used as single-photon sources: atoms or ions in the gas phase and, in condensed matter, organic molecules, defect centres, semiconductor nanocrystals and heterostructures. As new generations of sources are developed, coupling to cavities and nano-fabrication techniques lead to improved characteristics, delivery rates and spectral ranges. Judging from the brisk pace of recent progress, we expect single photons to soon proceed from demonstrations to applications and to bring with them the first practical uses of quantum information.
Light is often characterized only by its classical properties, like intensity or coherence. When looking at its quantum properties, described by photon correlations, new information about the state of the matter generating the radiation can be revealed. In particular the difference between independent and entangled emitters, which is at the heart of quantum mechanics, can be made visible in the photon statistics of the emitted light. The well-studied phenomenon of superradiance occurs when quantum-mechanical correlations between the emitters are present. Notwithstanding, superradiance was previously demonstrated only in terms of classical light properties. Here, we provide the missing link between quantum correlations of the active material and photon correlations in the emitted radiation. We use the superradiance of quantum dots in a cavity-quantum electrodynamics laser to show a direct connection between superradiant pulse emission and distinctive changes in the photon correlation function. This directly demonstrates the importance of quantum-mechanical correlations and their transfer between carriers and photons in novel optoelectronic devices.
Spectroscopy based on individual-photon-level light sources brings new variables to both spectroscopy and imaging. We refer to this approach as quantum-light spectroscopy (QLS). The photon statistics of different types of photon sources and photon entanglements are briefly described. We then illustrate the potential of QLS by means of some current experimental examples including time-resolved spectroscopy performed with single photons and quantum-enhanced optical imaging, showing how all the methods rely on correlations between entangled photons in the pair. We then ask: how might physical chemists exploit QLSs to expose new physical insights? For example, can we address fundamental questions in interactions between light and molecules or materials that are very difficult to address with classical light sources? Does QLS open up techniques to study highly congested spectra with higher combined spectral and temporal resolution than is possible with classical light? The concept of QLS also opens the potential study of fundamental questions such as what initial excited states are produced by individual photon absorption? We also point out the experimental challenges in extending QLS to more complex spectroscopies, such as multidimensional spectroscopies. We conclude with a brief selection of recent theoretical proposals to extend the capabilities of the QLS.
Introduction Quantum optics provides a complete description of the resonant interaction of light and a material system. The light scattered as a result of this interaction – the resonance fluorescence – provides a means to monitor and affect the material system's dynamics and also allows for the generation of nonclassical states of the electromagnetic field. Initial theoretical studies characterizing resonance fluorescence addressed fundamental questions regarding the necessity of quantizing the electromagnetic field. This is a particularly illustrative period in optical physics where multiple theories existed that might describe resonance fluorescence – semi-classical optical Bloch equations [1, 2] or quantum electrodynamics [4, 3] – and experimental evidence was necessary to identify the appropriate theoretical framework. Indeed, experiments in 1974 and 1977 investigating the resonance fluorescence lineshape [5, 6] and the photon statistics of the scattered light [7] vindicated the full quantum electrodynamical description of light-matter interaction over other models. In the subsequent 30 years, resonance fluorescence has been used as a high-resolution spectroscopic probe of a variety of physical systems, as a means to investigate quantum coherence in atomic gases and, with the current interest in quantum information science (QIS), as a tool for quantum-state preparation, measurement and control in trapped ions [8]. During this same time period, advances in material science have ushered in an era where it is possible to grow and fabricate solid-state devices at length scales commensurate with the quantum confinement of electrons and holes. It is only recently that resonance fluorescence has been observed from the prototypical artificial nanostructure exhibiting three-dimensional quantum confinement – a single semiconductor quantum dot (QD) [9].