In the realization of ultrasmall semiconductor lasers, cavity-QED effects are used to enhance spontaneous emission and enable the lasing threshold to be crossed with gain contributions from only a few solid-state emitters. Operation in this regime fosters correlation effects that leave their fingerprint especially in the emission dynamics of nanolasers. Using time-resolved photon-correlation spectroscopy, we show that in a quantum-dot photonic-crystal nanolaser emitting in the telecom band, second-order coherence associated with lasing is established on a different timescale than the emission itself. By combining measurements with a microscopic semiconductor laser theory, we attribute the origin to carrier-photon correlations that give rise to non-Markovian effects in the emission dynamics that are not captured by laser rate-equation theories. Our results have direct implications with respect to the modulation response, repetition rate, noise characteristics, and coherence properties of nanolasers for device applications.
© 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement
The quest for miniaturization of integrable and energy-efficient optoelectronic devices has led to the development of semiconductor nanolasers with increasingly smaller footprints and nearly thresholdless operation . Optical microcavities are used to confine the electromagnetic field to the extent of the wavelength, including photonic-crystal (PhC) cavities that combine a small mode volume with a long photon storage time. The small mode volume places a limit on the amount of gain material that can be brought into spatial overlap with the mode. To acquire sufficient gain to sustain lasing, spontaneous emission is enhanced via the Purcell effect [2,3], pushing the concept of lasing into a cavity-QED regime governed by photonic and electronic correlation and fluctuation effects [4–9].
The influence of correlations on lasing is not easily revealed, but it most often manifests in the dynamical properties of the emission, especially following a short excitation pulse. Here, we show that in a semiconductor nanolaser, carrier-photon correlations—enhanced by cavity-QED effects—lead to a breakdown of the traditional lasing picture in which coherent emission is directly related to the presence of stimulated emission. Using a modified Hanbury Brown and Twiss (HBT) experimental setup, we measure the time-resolved emission dynamics of a quantum-dot (QD) PhC nanolaser, which provides a complete two-time map of the second-order intensity correlation function,1.
The experimental results are confirmed by microscopic calculations of the output intensity and photon autocorrelation function. In the theory, both quantities obey different dynamical equations. At the lasing threshold, the dynamics of the output intensity are primarily determined by stimulated emission, while follows carrier-photon correlations that are analogous to stimulated emission but in the presence of an additional photon. Here, we show that the individual time dynamics of these higher-order correlations determining , but not the emission intensity, are responsible for the delay in coherent emission in a non-Markovian manner. This effect is facilitated by the combination of a high cavity-quality factor and a small amount of gain provided by a few solid-state emitters in the PhC nanocavity.
In Section 2, we characterize our PhC laser with a temperature-tunable gain and show input-output curves in the light-emitting diode (LED) and lasing operational regimes. In Section 3, the microscopic laser model that provides access to the laser and photon-correlation dynamics is introduced. Maps of the two-time autocorrelation function are presented in Section 4. The two-time diagonal provides the zero-delay photon autocorrelation function, which reveals the novel effect of delayed coherence formation presented in Section 5.
2. NANOLASER CHARACTERISTICS
A. Sample Characterization and Temperature Tuning of the Emitter Number
The nanolaser gain material comprises a single layer of InAsP QDs at the center of a 320 nm thick InP layer grown by metal organic vapor phase epitaxy [10,11]. The QD density is on the order of . A hexagonal PhC structure with a lattice constant of and an air-hole radius of is fabricated using electron-beam lithography, a plasma-etching process to form the PhC, and wet etching to suspend the InP membrane. A high- cavity is formed from three missing holes (-type defect cavity), yielding a nanocavity with an effective mode volume of containing on the order of few tens of QDs. The position of the two holes forming the end mirrors of the cavity have been displaced outward by to enhance the cavity . Measurements of the cavity linewidth, shown in Fig. 2(a), yield , which is the resolution limit of the spectrometer. While this places a lower bound of 50,000 on the factor at all temperatures, from our theoretical analysis we estimate a value that is approximately three times higher, corresponding to a cavity lifetime of . The QD spontaneous-emission lifetime measured in an unpatterned region of the device is between 5 K and 100 K (see Supplement 1). Within the PhC cavity, the combination of low cavity mode volume and high factor leads to a significant Purcell enhancement. By comparing dynamical measurements with a microscopic semiconductor model, excellent agreement is obtained for a cavity-modified lifetime of 305 ps at 300 K, implying a Purcell factor of around five.
An important aspect of our device is the ability to control its emission and photon correlation statistics by temperature-tuning the number of QDs that couple to the laser mode. From 5 K to 300 K, the center of the QD spontaneous emission shifts from 1540 to 1580 nm and the linewidth broadens from to . Figure 2(a) illustrates how the center of the inhomogeneous ensemble is strongly detuned at low temperatures (black). Feeding into the cavity mode is provided by only a few resonant emitters and is likely aided by off-resonant coupling of detuned background emitters through a quasicontinuum of excitonic transitions due to the complex multi-exciton level structure in the QDs [12–14]. At room temperature, a strong overlap of the emitter ensemble with the cavity mode is observed (red) and, from the theory, we estimate that emitting dipoles efficiently couple to the laser mode.
B. Input–Output Characteristics
The nanolaser is held in a vacuum in a closed-cycle cryostat with a variable temperature from 4 K to 300 K. Optical excitation is provided by a Ti:sapphire laser emitting 1 ps pulses centered at 805 nm at an 82 MHz repetition rate. A 0.5 numerical-aperture objective is used to focus and collect infrared light from the device. Emitted light is spectrally filtered with 2 nm bandwidth centered at the cavity resonance and then coupled into a single-mode optical fiber.
The input-output device characteristics are shown for different temperatures in Fig. 2(b), with the excitation pulse area and the integrated emission intensity plotted on the horizontal and vertical axes, respectively. At room temperature (red circles), the typical S-shaped curve is indicative of a clear transition from primarily spontaneous emission (LED operation) to lasing, separated by a threshold region that extends over nearly one order of magnitude in excitation power. Such smeared-out threshold behavior is characteristic of cavity-enhanced high -factor devices from which a large fraction of spontaneous emission is into the lasing mode . Importantly, the integrated output intensity saturates at the highest excitation powers (i.e., the laser mode is fed by a limited number of saturable emitters). By lowering the temperature, the attainable gain is reduced by QDs being tuned out of resonance with the laser mode. At 100 K (blue symbols), the emission intensity saturates already during the threshold, and a threshold appears to be fully absent at 5 K (black symbols). In this case, the gain saturates completely before a sufficient number of intracavity photons are present to initiate lasing. In Section 4 and in Supplement 1, we present photon autocorrelation measurements confirming that at temperatures below , the device operates in this type of LED regime and behaves as a thermal light source with at all times during the emission pulse.
To further confirm our claim of a gain-tunable QD nanolaser, we invoke a microscopic semiconductor laser theory that provides access to the full emission and correlation dynamics in a quantum-optical framework. Before the model is introduced in the following section, we interpret the input–output characteristics based on the theoretical results shown as solid lines in Fig. 2(b). Overall excellent agreement is achieved with a single parameter set for the device that is provided in Supplement 1. To accommodate the temperature tuning of the gain, the involved emitting dipole number is changed from 240 (300 K) to 10 (5 K). Simple rate-equation models relate the jump in the emission intensity at the threshold to the factor . Here, it is worth noticing that we use a temperature-independent value of . The reduction of the jump when lowering the temperature from 300 K to 100 K might be intuitively attributed to an increased factor, but is in fact caused by the onset of saturation before the threshold is fully developed . The factor itself is determined by the ratio of spontaneous emission channels and is therefore not expected to change much with the temperature.
A factor of 0.04 corresponds to photons in the cavity at the lasing threshold. A large factor for nanolasers is in contrast to macroscopic () and mesoscale () lasers with significantly more gain material and cavity photons at the threshold . Consequently, in nanolasers the emission and photon statistics are particularly sensitive to large relative fluctuations in the photon number, which scale as and can be as large as 40% for our device . In QD nanolasers with high factors similar to that presented here, large fluctuations in the photon number are responsible for strong intensity and timing fluctuations that are correlated, leading to a departure from coherent and Poissonian statistics in the emission dynamics [8,20] that are presented in Section 4. Before discussing the details of these measurements, we first introduce the theory used to access the emission and photon-correlation dynamics.
3. THEORETICAL MODEL FOR THE LASER EMISSION AND PHOTON CORRELATION DYNAMICS
The characterization of nanolasers in terms of the statistical properties of the emission (photon correlations) requires a treatment beyond rate-equation approaches. The cluster-expansion method has proven to be a reliable scheme to systematically include carrier and photon correlations and to map out their influence on the dynamical and steady-state properties of semiconductor nanolaser devices [21–24]. Particularly at low temperatures, our device operates deep in the cavity-QED regime, in which few emitters () couple to a high- cavity mode. In this regime, spontaneous emission plays an important role even at and above the threshold. By using the quantized electromagnetic field, spontaneous emission arises naturally, and dynamical equations for carrier–photon and photon–photon correlation functions give access to the photon autocorrelation function .
From the semiconductor Hamiltonian, a set of coupled equations of motion are derived for the mean photon number in the laser mode and the electron and hole fractional populations in the lasing level of the QDs,
Here, represents the photon escape rate, denotes the light–matter coupling constant, is the number of emitting dipoles in the cavity, and and are the creation (annihilation) operators for the carriers in the s-shell conduction- or valence-band state of each QD emitter. The cavity field is addressed by the Bosonic operators and . The quantities contain the scattering rates of carrier excitation from energetically higher p-states into the lasing level of the dots. The spontaneous loss of carriers into nonlasing modes at rate , together with and the dephasing and cavity-loss rates, implicitly define the factor that quantifies the ratio of the spontaneous emission in the photonic mode relative to the total spontaneous emission. Details and a derivation are given in Supplement 1.
Both the mean photon number and the carrier population dynamics (2)–(3) are driven by the photon-assisted polarization that describes an interband transition via the emission of a photon into the laser mode. Its dynamics follows a separate equation of motion,21] for more details). Rate equations can be obtained by adiabatically eliminating the dynamics of the photon-assisted polarization while neglecting higher-order carrier–photon correlations that contribute to stimulated emission in the second line ; however, the dynamical evolution of these correlations plays a central role in understanding the formation of coherent emission in Section 5.
Accessing the two-time second-order photon correlation function given by Eq. (1) is a two-step process. First, the zero-delay value is obtained by augmenting the dynamics of Eqs. (2)–(4) with that of additional carrier–photon correlation functions , , and . In a second step, the two-time map of is obtained by solving a time evolution with respect to the delay-time at each time step . Details of this procedure are given in Supplement 1.
4. PHOTON CORRELATION DYNAMICS
Photon correlation dynamics are measured using a modified HBT interferometer that provides access to the full two-time photon correlation function. This approach is similar to a previous study examining single-photon purity from a single QD . A schematic illustration of the setup is shown in Fig. 3. The light emitted from the nanolaser is spectrally filtered, split using a fiber-based 50:50 beam splitter (BS), and then measured with WSi superconducting nanowire single-photon detectors (SNSPDs) with a timing jitter of full-width at half-maximum (see Supplement 1). Photon arrival times and at the two SNSPDs are recorded relative to the Ti:sapphire excitation pulse. The time-tagged data are post-processed to construct dual start-stop correlation histograms that provide a complete mapping in and of the second-order photon correlation function (see timing diagram in the inset to Fig. 3). Measured and calculated two-time maps of are presented in Fig. 4 for the LED (5 K) and lasing (100 K) operational regimes of our device at the highest excitation powers , as indicated by the arrows in Fig. 2(b). The full two-time characteristics as obtained from experiment (top row) and theory (bottom row) are in reasonable agreement which, to the best of our knowledge, has not been presented before.
The maps can be interpreted by revisiting Eq. (1). The numerator describes the relative probability of detecting two photons at times and . The denominator describes the probability of detecting two photons at and , assuming these two photons are uncorrelated with one another (see Supplement 1). Because our source is pulsed, the temporal dynamics of do not reduce to a simple single-time dependence on , as they would for a stationary source . This can be seen by taking a slice along the diagonal line in Fig. 4 for which is fixed. The diagonal line through the origin shows the dynamics for .
As an example, at 100 K, see the right panel of Fig. 4(a). If one photon is detected at , then the likelihood of a second photon being detected at (0.5 ns) is higher (lower) than it would be for a coherent state with the same temporal intensity profile. Slices along the diagonal for are shown (points) together with the emission intensity (solid lines) for the LED and lasing operational regimes of our device in Figs. 5(a) and 5(b). The selected excitation powers , , and are indicated by the arrows in Fig. 2(b) and, in the case of the device operating at 100 K, correspond to below, at, and above the threshold. Theoretical results are provided in Fig. 5(c). At 5 K (panel a), throughout the entire pulse and does not change significantly with excitation power, as is expected for a thermal light source. Although an ideal value of two is expected for thermal emission, smaller values are observed, possibly due to the temporal resolution of the HBT experiment (see Supplement 1).
At 100 K, sufficient gain leads to the development of a threshold region in the input–output curve in Fig. 2(b). This interpretation is confirmed by the autocorrelation measurements in Fig. 5(b). Below the threshold (), at all times, whereas a value of one is reached during the emission pulse at higher excitation powers , confirming that the carrier density is high enough to drive coherent emission. It is noteworthy that under pulsed excitation, the emission pulse of a nanolaser undergoes various stages: After carriers have been created by the excitation pulse, the confined QD states that feed the laser transition are filled by carrier scattering on a timescale of the carrier relaxation time . Already during the relaxation process, spontaneous thermal emission begins as soon as carriers populate the lasing levels (rising edge of the emission pulse). At the peak of the emission pulse at time , the photon density in the cavity mode is at its highest value, and one would readily expect coherent emission with due to stimulated emission. However, a closer examination of the data shown in Fig. 5 reveals a significant temporal delay between the maximum of the emission peak and the formation of coherent emission expressed by the minimum in the autocorrelation function.
We find that the delay increases from to with temperature in the measurements and theory, leading to the high-intensity portion of the pulse being largely thermal despite the system operating in the regime of stimulated emission. These dynamics are in marked contrast to a previous study of a QD micropillar laser with , in which the onset of coherent emission coincides with the onset of stimulated emission at the pulse intensity maximum .
5. NON-MARKOVIAN DELAY OF SECOND-ORDER COHERENCE IN HIGH- NANOLASERS
Since the coupled equations of motion of the microscopic laser model accurately reproduce the observed delay in the formation of coherence, more insight can be obtained from theory. Equations (2)–(4) already show that the photon production does not adiabatically follow its source (namely spontaneous and stimulated emission), but is determined by the photon-assisted polarization that has its own dynamical evolution given by Eq. (4). A similar relationship exists  between the higher-order photon-correlation function that determines , and the higher-order photon-assisted polarization that describes interband recombination and the emission of a photon in the presence of an additional photon. This process obeys the time evolution ,
An understanding of the origin of delayed coherence formation can be obtained by identifying the dominant contributions to the time evolution of both polarizations, Eqs. (4) and (5), at the onset of lasing, given by the terms . While the time evolution of the photon production follows the polarization via the carrier inversion term , the evolution of the higher-order polarization is driven by correlations between carriers and photons . These carrier–photon correlations obey their own time evolution, which differs from that of the carrier populations,
In Fig. 6, the dynamics of the remaining equations of motion (blue dashed curve) are compared to the full dynamics (blue solid curve). Evidently, when the correlation dynamics are eliminated in a Markovian sense, the delay disappears and the maximum of the emission peak coincides with the minimum of the autocorrelation function (blue dashed curve). Therefore, this confirms our initial assertion that the traditional lasing picture, in which coherent emission is directly related to the presence of stimulated emission, is too simple. Instead, the photon number and its fluctuations respond to microscopic polarizations, and these develop on different timescales due to the presence of carrier–photon correlations, causing the observed effect.
Finally, we identify the delay in coherence formation as a property of high- nanolasers that is generally absent in conventional laser devices. In Fig. 7, the delay is plotted against the cavity- factor for three different sets of parameters that are representative of typical laser systems and, in particular, the number of involved emitting dipoles. As a general trend, a delay begins to form for -factors above 10,000 and can, in principle, become as large as 0.5 ns in cavities with extreme factors, such as microsphere or whispering-gallery mode resonators . Lower- cavities require a larger amount of gain material to cross the threshold, which is why the curves for 20, 75, and 240 emitters set in at a minimum -value. Below this value, stimulated emission is not reached, and the system operates as an LED. In the bad-cavity regime, lasing can be reached with sufficient gain material and the absence of a delay. Then, a Markovian description of the laser dynamics, in which coherence forms as an instantaneous response of the photonic field to stimulated emission, is justified.
A QD-PhC nanolaser has been demonstrated to operate in regimes of LED and laser emission by temperature-tuning the amount of gain material that couples to the laser mode. Photon correlation spectroscopy with high temporal resolution and microscopic laser theory have been combined to reveal a non-instantaneous response of the photon-autocorrelation function to the onset of stimulated emission. As a result, the emission pulse of our nanolaser is largely thermal and becomes coherent with a delay of 250 ps after the emission-pulse maximum has been reached at the peak of stimulated emission. The origin of this effect lies in the non-Markovian dynamics of microscopic polarization that is the response of the gain material to spontaneous and stimulated emission. While the effect plays no role in the bad-cavity regime of conventional lasers, it is of central importance in the design of cavity-QED enhanced nanolasers that operate with little gain material in high- cavities with . This new dynamical effect should stimulate further investigations into the modulation response of such devices.
Deutsche Forschungsgemeinschaft (Dfg).
See Supplement 1 for supporting content.
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