Controlling light–matter interaction strength is a highly important objective in many fundamental aspects of science and relevant applications. Being inherently small, the fine-structure constant α is responsible for light–matter interaction dynamics and the rates of related quantum processes. However, a structured electromagnetic environment is capable of modifying and tailoring these dynamics quite significantly by introducing new interaction channels [1]. There are two main approaches to control the structure of free-space fields—the first one is to create a cavity capable of concentrating electromagnetic energy. Cavity quantum electrodynamics (CQED), having a well-understood theoretical background, keeps inspiring investigation of new effects and experimental realizations. Numerous dielectric, plasmonic, and other types of structures have been realized, uncovering various types of light–matter interactions [2–5]. The second approach to manipulate quantum processes is to increase the light–matter interaction length. A typical layout in this case relies on a waveguide, supporting a long-distance propagation of electromagnetic waves without diffraction losses [6,7].

Over the past several decades, fiber technology has progressed a long distance from the rolled fiberglass to photonic crystal fibers (PCFs). Originally, step-index optical fibers were designed for information and communications technology. However, the advent of PCFs has led to extending their applications to many other areas, while advances in additive manufacturing techniques have the potential to shift fiber technologies to new frontiers [8,9]. PCFs consist of a set of microstructured capillaries running along the entire fiber length in order to suppress light escaping from the fiber core due to a photonic bandgap (bandgap PCFs), topological effect (kagome PCFs), or negative curvature phenomenon [antiresonant PCFs (AR-PCFs)]. Low optical losses and a large analyte–light interaction volume have stimulated using PCFs in such realms as photochemistry, optomechanics, biomedical and chemical sensing, and many others [10–12].

In order to increase the interaction strength between an analyte and propagating modes in a solid-core fiber, the jacket can be removed and leaking near fields are made accessible. However, a configuration where a field inside the fiber core overlaps with the matter suggests significant improvement of the interaction strength. It has been shown that hollow-core fibers can be used as spectrofluorimetric systems in which sample solutions are excited within the microstructure of the fiber [13–15]. Another notable spectrum of PCF applications can be achieved via functionalization of the fiber inner structure. For example, deposition of composite materials on the inner surface of PCF’s structure can tune the fiber light guiding properties in a controllable fashion [16,17]. Hence, comprehensive studies of factors affecting light–matter interaction dynamics inside a fiber could enable further advances in the field.

In our work, we use a so-called free-boundary AR-PCF [Fig. 1(a)], where the dynamics of light–matter interactions are governed by two main factors. The first factor is the propagation of light along the fiber. The second one is the transverse confinement, associated with the design of the internal structure. In order to probe those mechanisms, we have deposited halide perovskite nanocrystals on the fiber capillary walls and investigated the impact of the fiber structure on their fluorescent properties, including changes in the emitted light intensity and fluorescence lifetime.

The manipulation of the spontaneous emission rate of an emitter via modification of the surrounding electromagnetic environment is known as the Purcell effect [18]. The radiation Purcell factor (Frad) is defined as the ratio between the decay rates in a structure (γ) and the free-space value (γ0). This ratio is directly linked to the local electromagnetic field and enables probing the latter by investigating the fluorescent properties of light emitters [19]: Frad=γγ0=1+6πε0|d¯1|21q3Im[d¯1*⋅E¯s(r¯d)],(1)where q=ω/c is a free-space wavenumber, E¯s(r¯d) is the scattering part of the electric field, produced by a point radiating dipole, and positioned at (r¯d), d¯1 is a dipole moment corresponding to an oscillating frequency ω0 (central emission frequency of a quantum system). Note that the Purcell factor in a nontrivial electromagnetic environment is not a scalar and rather depends on the orientation of a radiating dipole moment with respect to a medium.

It is quite remarkable that the classical-quantum correspondence principle, based on a local Langevin quantization, allows the calculation of spontaneous decay rates and other higher-order phenomena with classical electrodynamic tools (e.g., Refs. [1,20,21]). In fact, the calculation of E¯s(r¯d) in Eq. (1) can be obtained with a numerical modeling, which can be implemented in a number of commercially available packages. While Eq. (1) addresses a hypothetical case of a perfect emitter with a quantum yield equal to unity, nonradiative channels can be introduced to the formalism phenomenologically. Considering the balance between the radiated and dissipated energies and assuming a weak coupling regime with radiative decay dynamics described with a single exponential contribution [22] (I=I0e−t/τ), the overall Purcell factor can be written as F=Prad+PnonradP0,rad=Frad+Fnonrad,(2)where Prad is the radiated power, and Pnonrad is the power dissipated in the environment and in the emitter itself. P0,rad is the radiated power in the case when the emitter is placed in free space (less than unity quantum yields can also be introduced here). It is worth noting that all of the quantities in Eq. (2) can be straightforwardly calculated by surface flux integration of a Poynting vector and volumetric integration of Joule losses. The latter can be defined as P=ω2ε0∫d3r′Im[ε(r′)]E¯(r′)2 [21]. A numerical routine for calculating the Purcell factor in the fiber was implemented by adopting the impedance approach, which allows these factors to be taken into account simultaneously [23].

The fiber modes have been calculated by a finite element method (FEM). They can be divided into two groups: cladding or leaky modes and core (guided) modes. In our work we consider the fundamental core mode (LP01) and a mixture of cladding modes. Numerically calculated core and cladding mode field distributions and their effective indices are shown in Figs. 2(a) and 2(b). Experimentally, the fundamental mode was excited by overlapping a weakly focused Gaussian beam at a wavelength of 485 nm with the fiber core, while leaky modes were excited by shifting the beam to the fiber cladding. Due to the short fiber length (several centimeters), these modes were detected with a CCD camera from the output fiber facet [Figs. 2(c) and 2(d)] (additional experimental details will be provided hereinafter). The resulting interference is the result of the excitation of a set of leaky modes, which have different mode profiles with very close effective indices. The calculated effective index has a real part close to 1.4499. Since fundamental and leaky modes are spatially well separated, they can be probed individually by spatial filtering in the image plane.

Spontaneous emission rate is inversely proportional to the group velocity [24], and when the modal dispersion is negligible it grows linearly with the modal effective index. Consequently, a higher mode index for the cladding modes is expected to result in a higher Purcell factor compared to the case of the guided core mode with a near-unity effective index.

CsPbBr3 nanocrystals (NCs) were synthesized by using similar procedures reported by Protesescu et al. [25]. 0.4 g of caesium carbonate (Cs2CO3, Sigma-Aldrich, 99.9%), 20 mL of 1-octadecene (ODE, TCI, >90%), and 1.25 mL of oleic acid (OA, Vekton, 90%) were added into a 50 mL single neck flask and stirred vigorously for 5 h at 120°C in a N2-filled glove box with O2 and H2O level not exceeding 1 ppm (parts per million). Then the temperature was raised up to 150°C, and the mixture was kept until Cs2CO3 reacted with OA to afford a clear solution. 69 mg of lead (II) bromide (PbBr2, Alfa Aesar, Puratronic, 99.999%) and 7 mL of ODE were added into a 50 mL three-neck flask and stirred vigorously for 1 h at 120°C under vacuum. Thereafter, vacuum conditions were changed to bubbling under N2 gas and 0.5 mL of OA and 0.5 mL of oleylamine (OLA, Acros, 80%–90%) were rapidly injected into the mixture to dissolve PbBr2 and to afford a pale yellowish solution for 1–2 min. Then the temperature was gradually increased by 6°C/min, and, once it reached 180°C, 0.5 mL of CsOA in ODE preheated at 120°C was rapidly injected in the solution. Immediately, a fluorescent colloid solution was formed and allowed to react for 6 s until it was cooled down in an ice bath. The cooled solution was poured into a centrifuge tube and centrifuged at 5000 r/min for 5 min. Then the supernatant solution was discarded, and the precipitant, which is aggregated CsPbBr3 NCs, was dispersed in 20 mL of toluene. To fill in AR-PCF with CsPbBr3 NCs, we kept the colloid solution overnight to allow precipitation of the aggregates and used an upper transparent fraction.

The photonic crystal fiber was fabricated at the University of Bath using the stack-and-draw technique [26]. Hollow silica capillaries are placed inside a silica jacket tube and supported by additional glass tubes at either end, creating a preform containing a single ring of seven separate capillaries around a hollow core. This preform is then drawn to fiber via an intermediate cane stage in which the capillaries become fused to the jacket. In the final draw stage differential pressure is applied to the core and the capillaries to yield control over the degree of inflation and hence the dimensions of the cladding structure. Thus, we create fiber in which the thickness of the single silica layer adjacent to the core is very well controlled and supports guidance of core modes in wavelength ranges that are in antiresonance with the core–cladding boundary [27]. The AR-PCF used in this work has a core size of approximately 30 μm, capillaries 12 μm in diameter, and a cutback measurement over 60 m of fiber reveals a transmission window around 600 nm wavelength with attenuation below 0.25 dB/km between 550 and 650 nm. The short length of AR-PCF used in the experiments presented here enables transmission over a slightly broader wavelength range.

The AR-PCF was glued into the syringe needle using mounting wax (Apiezon W Wax). The needle with the fiber glued inside was attached to a luer syringe filled with solvent or particle suspension, and constant pressure was applied. The perovskite quantum dots were deposited inside the AR-PCF using a two-step process. First, the fiber was washed with toluene for 1 h in order to improve adhesion of perovskite dots to the fiber surface. Second, the particle solution in dimethyl formamide was rinsed through the fiber for 30 min. After the perovskite crystal deposition, the fiber was flushed with dimethyl formamide for 30 min to remove excess crystals, and the fiber was put on hotplate at 100°C for 2 h to remove excess solvent from the fiber core. After the dots’ deposition, both ends of the capillary were cleaved to avoid crystalline deposits on the fiber facets.

The deposited perovskite NCs inside the AR-PCF were characterized by SEM and confocal scanning laser microscopy (CLSM) as shown in Fig. 3. It is noteworthy that there were no large clusters of perovskite nanoparticles, and the perovskite nanoparticles were located on all capillary surfaces with the size of individual crystals ranging between 20 and 50 nm.

CLSM data was obtained using a Leica DM8 microscope with a 20× objective (NA = 0.75). The excitation was performed at 488 nm, and the fluorescence was detected with the filter set to a 505–530 nm window. The cleaved AR-PCF was mounted on a holder to measure a Z-stack. Figure 3(c) shows a single cross section of the acquired stack. It can be seen that the fluorescence intensity distribution varies between individual capillaries, which can be caused by constrained flow of the solution in one of the smaller capillaries. The three-dimensional reconstruction of perovskite fluorescence also shows that one of the capillaries has significantly smaller filling fraction of emitters [Fig. 3(d)].

It should be noted that lack of aggregates justifies the use of suggested analytical model for Purcell factor assessment—the individual crystals are well separated from each other and small enough to be considered as point radiation sources.

A schematic of the experimental setup is depicted in Fig. 4. The spectrally filtered supercontinuum laser (YSL SC Pro with VLF filter, excitation band 480–490 nm) is coupled to the AR-PCF with perovskite quantum dots with a 4× objective. The excitation power was attenuated to levels, when the shape of the lifetime curve of the dots was not changed. The light was outcoupled from fiber using a 20× objective, the excitation was suppressed using a 500 nm longpass filter (Semrock), and background rejection was improved using a spatial filter (1:1 telescope with 200 μm pinhole in the focal plane). The fiber facet was imaged using an f=200mm lens and split by a 50:50 beam splitter between the CMOS camera and the fiber-coupled spectrometer (Andor Kymera 193) with a single-photon counter (MicroPhotonDevices). The lifetimes were obtained using time-tagging electronics (TimeHarp 260, Picoquant) and analyzed using dedicated software (Fluofit, Picoquant).

Time-correlated single-photon counting was employed to measure lifetime changes of perovskite NCs deposited on the fiber capillaries. The experimental layout appears in Fig. 4(a) and contains two main parts—coupling of excitation light into the PCF and collection of the transmitted light. The output fiber facet is imaged with the objective, and perovskite NCs emission is analyzed. Optical signals were collected with a fiber mounted on a motorized stage. The aperture of the collection fiber acts as a spatial filter, which enables assessing the contribution of different modes to the overall interaction phenomenon.

Lead halide perovskite NCs were chosen for the experiment. Such materials have chemical formula ABX3, where A (cation) stands for organic or inorganic cations, B is lead, and X is replaced by I, Br, or Cl. Distinct features of lead halide perovskites are pronounced exciton resonance at room temperature and high quantum yield, which make them good candidates for probing local Purcell enhancement. By changing the anion composition, it is possible to tune the emission wavelength over the whole visible spectrum. Here the crystals were chosen to fit the transparency window of the fiber.

The impact of the AR-PCF modes hierarchy on the emission properties was analyzed by measuring the photoluminescence and luminescence decay rates of perovskite NCs. The schematic of the measurements is depicted in Fig. 4(a). The excitation light was coupled to AR-PCF, and the emission of the perovskite NCs was analyzed at different points at the AR-PCF cross section [Fig. 4(b)]: (1) core of AR-PCF, (2) capillary of AR-PCF, and (3) fiber cladding near the surface of the inner capillary. The fiber capillaries and core were flushed with toluene to improve adhesion of the perovskite NCs to the fiber glass.

Photoluminescence was excited by using a band-filtered supercontinuum light source centered around 470 nm with bandwidth of 10 nm. In order to avoid pump-dependent effects, the excitation power was decreased down to levels where no pump-dependent lifetime shortening was observed. The collected signal was spectrally filtered with a longpass filter to suppress excitation light and spatially filtered with a collection fiber in order to distinguish between signals coupled into different modes in the fiber.

Since the Purcell enhancement is position dependent [Fig. 1(b)] and the signal is collected from a large set of emitters coupled to core or cladding modes, initially a single exponential decay of an isolated nanocrystal becomes more complex, showing multiple emitters’ contributions (e.g., Refs. [28,29]). In order to account for this position and orientation dependence, decay curves were fitted using a multi-exponential model with deconvolution fitting, where an instrument response function (IRF) was used to factor in a finite duration of the pump pulse (under 150 ps) and overall delay in electronics responses. The time-dependent signal is I(t)=∫−∞tIRF(t′)∑i=1nAie−t−t′ti,(3)where I(t) is the time-dependent intensity of the measured signal.

Spontaneous emission spectra were measured first. Figure 5(a) shows the data for three collection points. While the spectral shapes are similar in all cases, the emission peak center exhibits a redshift when moving the probe point away from the fiber’s center. This effect is associated with self-absorption of emitted light, which is well known in perovskite nanowires [30–32]. Time traces of the luminescence decay for the probe points appear in Figs. 5(b)–5(d), making the direct comparison possible. The lifetimes (biexponential decay) for the perovskite quantum dots [blue curve in Fig. 5(b)] deposited on the glass were τ1=1.8±0.1ns and τ2=6.9±0.3ns, which are in good agreement with the values for colloid-synthesized perovskite quantum dots, reported in literature [25].

The first observation to be made is that the lifetime of perovskite quantum dots in the core is almost identical to the free-space scenario (the reference) as shown in Fig. 5(b). The reference measurements were taken by depositing a thin layer of perovskite dots on cleaned glass coverslip and by averaging over 10 measurements. This is fully consistent with both the modal and local Purcell approach, suggesting the enhancement to be negligible (close to unity). The shortest luminescence lifetime emerges from the emission coupled to the cladding modes as seen in Figs. 5(c) and 5(d).

In order to distinguish the difference between emission of quantum dots coupled to cladding modes and free-space emission, we calculate both intensity and amplitude-weighted lifetimes. The lifetimes at different points of interest on the fiber and of reference perovskite dots are summarized in Table 1. Here, for the sake of simplicity, we consider a multi-exponential decay model, where emission decay is described by Eq. (1). However, it should be noted that the more accurate description of charge-carrier recombination dynamics is given by the ABC model, which factors in multiple-particle recombination effects [33].Table 1.

Summary on Lifetime Data Extracted from PL Decay Curves

The analysis of the impact of the Purcell effect on quantum dot emission was carried out for averaged values of lifetimes [34], intensity-weighted and amplitude-weighted, which are described with the following relations: ⟨τamplitude⟩=∑Ajτj∑Aj,(4)⟨τintensity⟩=∑Ajτj2∑Ajτj.(5)

Following Ref. [35], intensity-weighted lifetimes are used for the Purcell factor analysis owing to their lower sensitivity to the fitting model.

Table 2 summarizes the values of Purcell factor calculated for different modes, propagating in the fiber. The lowest value is observed for the core-coupled modes, yielding value of P=0.92. The cladding modes exhibit higher values of Purcell factor of P=1.33 (for the modes outcoupled from inner capillary structure) and P=1.38 (for the modes outcoupled from cladding). The obtained values are in good agreement with numerical simulation result Pnumerical=1.33 for the quantum dots located in the vicinity of the capillaries.Table 2.

Purcell Factors for Different Modes of the Fiber

Finally, it is worth making the comparison between the local Purcell effect analysis and the modal structure. The latter approach uses an effective index as a single input parameter. Indeed, the modal description predicts no enhancement for emitters in the core and 1.45 for those coupled to the cladding. Comparing the results, it can be seen that both approaches agree with each other within ∼10%, nevertheless local Purcell analysis provides a better fit. This result demonstrates the impact of local structuring over the global response of the system. It is worth noting that the computational complexity favors the modal approach by far (a single 2D simulation versus a large number of full-wave 3D computations). Similar conclusions were drawn by expecting local interactions with, e.g.,  metamaterials [36,37].

Here we have compared those two approaches by investigating spontaneous emission processes inside an AR-PCF, functionalized with perovskite crystals. Hollow-core photonic crystal fibers, supporting long-distance light propagation inside a hollow capillary, have a rather complex internal structure. The latter complicates studies of light–matter dynamics of processes occurring inside the fiber. While local Langevin quantization of electromagnetic fields allows addressing interaction processes of any order, the modal description of propagation has a clear advantage of providing an intuitive description. Spontaneous emission, being the first-order quantum process, allows probing the local density of states, which is one of the key input parameters in any quantum model. Applying spatial filtering on a collected signal together with time-correlated single-photon counting, we reconstructed local Purcell enhancement in the fiber and compared it qualitatively with the effective index of core and cladding modes, which predicts higher Purcell enhancement for cladding modes. We found that local approach agrees with the experimental data within ∼10% and correlates with estimates. Local Purcell analysis demonstrates the impact of local structuring over the global response of the system and allows assessment of enhancement value qualitatively.