Abstract
We theoretically investigate the far-field scattering properties of multiphoton super- and subradiant states which can be prepared by multiphoton excitations with orbital angular momentum (OAM). Due to multiphoton interference, the far-field patterns of the subradiant modes show directional scattering along the excitation direction or transverse scattering with number of peaks equal to the number of atoms. When more atoms are involved, we consider structures of stacked and concentric rings, which respectively show enhanced directional scattering and smoothed emission patterns. Our scheme gives insights to prepare many-body subradiant states, and is potentially applicable to quantum storage of multiphoton with OAM. By designing atomic spatial distributions, these cooperative states can tailor the far-field emission properties, which is useful for light collections and quantum information manipulations.
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Introduction
Superradiance1,2 results from cooperative light-matter interactions, which typically radiates directionally3 with a shortened time scale. This enhancement of the spontaneous emission comes from the resonant dipole-dipole interactions (RDDI)4 induced by rescattered photons between atoms. In such strong coupling regime, subradiance on the other hand also becomes evident5 in the afterglow6 of the superradiance. The remnant radiation with slow decay rates signifies the presence of subradiant states, and at the same time, indicates that the initially excited superradiant state is not the eigenstate of the dynamically interacting system. This is due to the long-range nature of RDDI which couples every other atom in the system, and thus in general all Hilbert space of super- and subradiant states are involved in the dissipation process. This offers an opportunity to manipulate light-matter interacting systems7,8 and to deterministically access these subradiant states, for example, in one-dimensional9,10,11,12, two-dimensional (2D)13, or three-dimensional (3D) atomic arrays14,15 and 2D metamaterial16,17. In addition to neutral atoms, subradiant states can also be excited and prepared in two trapped ions18, molecules19,20,21, plasmonic nanocavities22, and atomic arrays in a cavity23.
In addition to the obvious linewidth broadening (superradiance) along with cooperative frequency shifts24,25,26,27,28,29 or narrowing (subradiance)5 in fluorescence experiments, collective light scattering in a dense atomic medium30,31,32 also provides useful information of cooperative light-matter interacting systems. Aside from well-known directional light scattering of superradiance, recently we propose to use helical-phase-imprinted (HPI) single-photon subradiant states33 on a ring array to investigate the far-field emission patterns. This subradiant state can be prepared by absorption of single-photon carrying the orbital angular momentum (OAM)34,35,36,37,38 and becomes the alternative candidate for storage of light quanta with OAM39,40,41. Similar ring-shaped lattice has been proposed to excite high-lying Rydberg states42 which lead to nonclassical collective photon emissions.
In this paper, we investigate the far-field scattering properties of HPI multiphoton subradiant states in the ring arrays, which are less studied systematically. The HPI multiphoton states can tailor and modify the radiation properties by controlling and engineering the atomic configurations and light polarizations. Thus, this is potentially useful in generating and detecting entangled multiphoton states43, and also offers opportunities in manipulating multiphoton resource in quantum network7.
Helical-phase-imprinted multiphoton states
When a resonant multiphoton source of M photons is absorbed by N two-level atoms (|g〉 and |e〉), a symmetric state can be formed, and such that M excited and N − M ground states are symmetrically distributed in all atoms with equal probabilities \({({C}_{M}^{N})}^{-1}\) where C denotes the binomial coefficients. To access the other possible multiphoton super- and subradiant states, we have proposed to use phase-imprinting methods to unitarily transform the system into15,
where n ∈ \([1,{C}_{M}^{N}]\) and \(f(\overrightarrow{\mu })={\sum }_{i=1}^{M}{\mu }_{i}\) indicates the linear increases of the imprinted phases in a 3D atomic array. We use a concise representation of the traveling phase k L ⋅ R M ≡ \({{\bf{k}}}_{L}\cdot {\sum }_{m=1}^{M}{{\bf{r}}}_{{\mu }_{m}}\) and define the bare states with M excitations, \(|{\psi }_{N}^{(M)}(\overrightarrow{\mu })\rangle \equiv |e{\rangle }_{{\mu }_{1}}|e{\rangle }_{{\mu }_{2}}\cdots |e{\rangle }_{{\mu }_{M}}|g{\rangle }^{\otimes (N-M)}\) with \(\overrightarrow{\mu }\) = (μ1, μ2, …, μ M ). Note that this specific construction of Hilbert space is not unique, and there are many ways to create such multiple excitations space. This phase imprinting method dynamically controls the incrementally increasing phases either by Zeeman field or a Stark field gradient pulse, but demands large field gradient strengths or long interaction time.
Nevertheless, this linearly increasing phase can be also imprinted in an azimuthal direction by light with OAM33 without external field gradients. We consider Laguerre-Gaussian modes of light excitations, which carries a phase dependence of eilϕ with a quantized OAM of lħ. For N ϕ equidistant atoms sitting on a single ring in Fig. 1, the light imprints the phase of \(\varphi =2\pi ({\sum }_{m=1}^{M}{\mu }_{m}-\mathrm{1)/}{N}_{\varphi }\) on the atoms for M excitations. To label the ring structures of concentric or stacked rings in Fig. 1(b) and (c), we raise up atomic indices to superscripts and denote μj = \(({\mu }_{r}^{j}-\mathrm{1)}{N}_{\varphi }\) + \({\mu }_{\varphi }^{j}\) or \(({\mu }_{z}^{j}-\mathrm{1)}{N}_{\varphi }\) + \({\mu }_{\varphi }^{j}\), respectively. The number of integrated rings is \({\mu }_{r,z}^{j}\) ∈ [1, Nr,z] where Nr,z represents the rings along \(\hat{r}(z)\) direction, and the total number of atoms becomes N = Nr,zN ϕ . For each atom labeled as j, \({\mu }_{\varphi }^{j}\) is within [1, N ϕ ]. Therefore, the light with OAM absorbed by the ring array forms HPI multiphoton states
where here we note that \({\overrightarrow{\mu }}_{\varphi }=({\mu }_{\varphi }^{1},\,{\mu }_{\varphi }^{2},\,\cdots ,{\mu }_{\varphi }^{M})\) and define \({{\bf{R}}}_{M}^{j}\equiv {\sum }_{j=1}^{M}{r}_{{\mu }^{j}}\) \({f}^{j}({\overrightarrow{\mu }}_{\varphi })\equiv {\sum }_{j=1}^{M}\,{\mu }_{\varphi }^{j}\). Here we propose to use Laguerre-Gaussian modes of \({u}_{p=0}^{l}(r,\varphi )\) with an arbitrary OAM eilϕ and zero radial index (p) to prepare HPI multiphoton states. For more technical details on excitation and preparation of the states, we explain in Supplemental Information.
Comparing Eq. (1), the HPI multiphoton states of Eq. (2) has limited imprinted phases by OAM of light since it puts phases along \(\hat{\varphi }\) direction only. Thus, equation (2) forms only a subspace of multiply-excited states of equation (1). However, HPI multiphoton states can expedite the preparation protocols by simply using light with OAM, which removes the requirement of external addressing fields and makes the proposed scheme here more efficient and dominant in generating multiphoton subradiant states. In the next subsection, we further derive the general expression for far-field emission properties of HPI multiphoton states, which we use to investigate the effect of multiphoton interference and atomic configurations on the emission patterns in the next section.
Far-field scattering
The far-field scattering patterns can provide a unique characterization of the HPI multiphoton states. The general expression of the far-field scattering from uniformly-polarized two-level atoms is4
where ω eg is the energy difference, \(\hat{{\bf{R}}}\)//k R denotes the observation direction, r αβ = r α − r β denotes mutual atomic separations, and the dipole orientation \(\hat{{\bf{p}}}\) is determined by the polarization of excitation field. Since the far-field scattering concerns the observation point way distant from the atoms, the radiation phase is then contributed by the retarded ones \({e}^{-i{{\bf{k}}}_{R}\cdot {{\bf{r}}}_{\alpha }}\) and |k R | = ω eg /c. At equal time of equation (3), we obtain the far-field radiation patterns from the HPI multiphoton states \(|{\varphi }_{l}^{(M)}(t){\rangle }_{{\rm{HPI}}}\),
where I0 (t) is the time-evolving fluorescence intensity and depends on the eigenvalues of the coupling matrix10,14,15. The multiphoton coupling matrix elements from RDDI can be seen in Methods and ref.15. An implicit dependence of multiply-excited configurations is in the spatial and imprinted phases respectively. equation (4) characterizes the far-field scattering property from the HPI multiphoton states created by an excitation field with lħ OAM, which involves the interplay of the atomic distributions \({{\bf{r}}}_{{\mu }^{j}}\) and the helical phases \(\propto \,{e}^{i2l\pi /{N}_{\varphi }}\). In the next section, we investigate the far-field scattering properties for the atomic configurations in Fig. 1 and various OAM of light.
Light scattering from HPI multiphoton states
Here we focus on HPI two- and three-photon states prepared in a single, stacked, and concentric rings. For M excitations, there are in general \({C}_{M}^{N}\) possible HPI multiphoton states. Before we investigate the case of many atoms, a few atoms study can illuminate the interplay between imprinted phases, atomic spatial distributions, and multiphoton interference.
Three- and four-atom case
For three atoms on a ring with the same arc length, we have the far-field scattering from HPI two-photon states from \(\hat{x}\)-polarized light,
where \(\bar{r}=\,|{{\bf{k}}}_{R}|r\) and c.c. means the complex conjugate of counterparts in the parenthesis. This far-field pattern is exactly the same as HPI single photon states, since the traveling phases contributed from atomic configurations in equation (4), \({{\bf{R}}}_{M}^{m}-{{\bf{R}}}_{M}^{j}\), involve only pairwise atoms. This is also the case for the difference of imprinted helical phases, \({f}^{j(m)}({\overrightarrow{\mu }}_{\varphi })\). Therefore, the far-field patterns of HPI multiphoton states with M = N − 1 exactly correspond to HPI single photon states on a ring33.
The unique emission pattern of HPI multiphoton states then emerges in two-photon states of a ring with four atoms. In Fig. 2, we show the scattering patterns Ω f (θ, ϕ) with associated fluorescence intensity I0 (t). Since the HPI multiphoton states are not the eigenstates of the system in general15, their fluorescence results from several eigen decay rates which we show in Fig. 2(c) for the specific atomic configuration with six \(({C}_{M}^{N})\) eigenstates. We then distinguish the sub- (l = 1, 2) from superradiant (l = 4) states by comparing I0 (t) with the intrinsic decay function e−2Γt. A clear signature of the subradiant far-field pattern is the side scattering30,31,33 in the mode of l = 1, while the superradiant mode of l = 4 typically shows a forward and backward scattering along the excitation direction \(\hat{z}\).
Interestingly, the most subradiant state of l = 2 shows not only small side scattering peaks at ϕ = π/2 and 3π/2, but also enhanced forward and backward scatterings, bearing both signatures of single-photon sub- and superradiance. This is in contrast to HPI single-photon subradiant states33 which allow only side scatterings. In addition, this illustrates the multiphoton interference in the HPI states, which carries an extra degree of freedom in phase-imprinting other than atomic configurations (traveling phases) and excitation modes (various l). We note that discrete C4 rotational symmetry in Ω f (θ, ϕ) is preserved for linear polarizations in the atomic system of N = 4 n with integers n. This can be seen as we change ϕ to ϕ + π/2 in the prefactor of equation (4), which changes \(\hat{x}\)-polarized emission pattern to \(\hat{y}\)-polarized one. Also l ↔ −l symmetry in Ω f (θ, ϕ) is sustained for all N as r → 0. In general for all r, even N preserves this mode symmetry. This mode symmetry emerges due to the regular convex polygon geometry which we assume for atoms forming a ring and incremental helical phases we apply, and as such the far-field scattering in equation (4) does not change as l → −l (or equivalently N − l). Therefore, Ω f (θ, ϕ) of l = 3 is the same as l = 1 in Fig. 2. For another example of N = 6 with M = 2, one of the far-field scattering contributions, cos [k R ⋅ (r1 + r2 − r3 − r4) + 2lπ × 4/6], pairs up with cos[k R ⋅ (r4 + r5 − r1 − r6) + 2lπ × (−2)/6], which interchanges to each other as l → −l.
Single ring
Here We take N = 12 on a ring as an example and investigate the far-field scattering patterns of HPI two-photon subradiant states. This N has C4 rotational symmetry so we use \(\hat{x}\)-polarized light without loss of generality. In Fig. 3(a1), we show the side scattering of the subradiant modes with l = 3, 4 and 5. The specific two-dimensional plot of l = 3 mode is illustrated in Fig. 3(b), which reveals N side scattering peaks. This specific mode corresponds to the number of atoms, similar for l = 1 mode in Fig. 2(a) and thus can be used to characterize the atomic configuration. The l = 6 subradiant mode in Fig. 3(a1), also similar to the l = 2 mode in Fig. 2(a), shows forward and backward scattering, but radiates in a rate only second to the most subradiant mode of l = 5. This can be seen in the time evolutions of the subradiant modes in Fig. 3(c) where l = 5 state evolves longer than the other subradiant modes since it occupies the most subradiant eigen decay rate. The HPI states of l = 3, 4 and 5 drop rapidly initially due to partial overlaps with the superradiant eigenmodes while later they still evolve past the intrinsic decay e−2Γt, indicating a subradiant afterglow. In the insets of Fig. 3(c), we show the effect from the fluctuations of atomic positions along the arc length on the fluorescence intensity. The oscillation peaks at a later time are smoothed out as the fluctuation increases, and the fitted exponential decay rates \(({e}^{-{\Gamma }_{f}t})\) of the mean radiation envelopes are Γ f /Γ = 0.419, 0.655, 0.663, respectively for free of, 5%, and 10% position fluctuations. This leads to the decrease of the effective lifetime of the HPI subradiant state, similar to the suppression of linewidth narrowing in the subradiant eigenmodes of 2D arrays with position fluctuations13. The averaged emission patterns are shown for l = 3 and 6 respectively in Fig. 3(a2) with 5% position fluctuations. The mode of l = 3 also shows the smoothing feature in the side peaks along with finite but less significant forward and backward scatterings, in contrast to Fig. 3(b) without position fluctuations. On the contrary for the mode of l = 6, the forward and backward scattering pattern is more resilient to the fluctuations. The clear side peaks of l = 3 can be restored as the fluctuation is reduced below around 1%.
For far-field scattering patterns of HPI three-photon subradiant states, we show in Fig. 4 with N = 8. We note that as N increases, the total Hilbert space goes up as \({\mathscr{O}}({N}^{3})\), so here we only focus on the feature of directional subradiance instead of multi-atom effect. For larger N on the other hand, we will investigate the effect of stacked and concentric rings in the next subsection. In Fig. 4, we show the effect of multiphoton interference on the far-field scattering, where the subradiant mode of l = N/2 encodes the information of N side scattering peaks, in contrast to forward/backward scattering l = N/2 modes in Figs 2 and 3. Furthermore, the subradiant mode at l = 3 in Fig. 4 shows an oblique scattering, instead of forward and backward directions.
The HPI multiphoton subradiant states show quite rich far-field scattering patterns. Except for side scatterings, the subradiant emission also allows along or near the excitation direction. In addition, the oscillation of time evolutions manifests the beating frequency from the differences of cooperative frequency shifts10. This shows flexibility to tailor and manipulate the emission time and directions of multiphoton states, and enables the one to one correspondence between the atomic configurations and the far-field scattering patterns.
Stacked and concentric rings
Finally we investigate the far-field scattering properties of HPI multiphoton subradiant states in the stacked and concentric rings. We have investigated these two configurations of HPI single-photon states33 which show enhanced forward scattering and narrowing effect on side scattering peaks in the stacked and concentric rings respectively. In Fig. 5, we show the far-field scattering properties of HPI two-photon subradiant states with l = 2 and 4, in the stacked and concentric rings respectively. Similar to HPI single-photon states, the forward scattering is enhanced in Fig. 5(c) and (e) as N z increases. On the contrary, comparing Figs 3(a) and 5(a), the transverse scattering peaks are smoothed out due to multiphoton interference. This smoothing effect is even more significant in the concentric rings of Fig. 5(d) as N r increases, and the states of l = 2 and 4 become superradiant for a larger N r . In Fig. 5(f), the effect of concentric rings weakens the forward-backward scattering along with emerging side scattering. Therefore, in the perspective of preparing multiphoton subradiant states in a large atomic system, the stacked rings are better than the concentric ones since the former allows a more directional emission pattern which is better for light collection and detection.
For HPI three-photon subradiant states, we show the results of Ω f (θ, ϕ) of two stacked rings in Fig. 6 as a comparison to Fig. 4. We find the enhanced oblique scattering toward the backward direction for l = 3 mode and narrowing side scattering peaks for l = 4 in polar angles θ. The small peaks at θ ≈ 3π/4 for l = 4 is also a signature of enhanced oblique scattering which breaks the mirror symmetry of the emission patterns in Fig. 4 with respect to \(\hat{x}-\hat{y}\) plane. We note that the clear N ϕ number of transverse scattering peaks disappear due to multiphoton effect. The time evolutions of these states in Fig. 6(c) shows the subradiant fluorescence, and the mode for l = 3 is more subradiant than the one in Fig. 4(c), which indicates the cooperative enhancement in subradiance when more atoms are stacked up. For more atoms, for example of N z = 3, we find similar enhancement in oblique scattering and narrowing polar angle distribution for l = 3 and 4 modes respectively. For concentric rings, these three-photon modes do not show significant subradiance, similar to Fig. 5(c) and (d).
Discussion
Recently there is a huge advance in precisely controlling atomic separations in waveguide44 or integrated color centers45 and in assembling discrete atoms by optical microtraps46,47, which has enabled fine tunings of light-matter interactions. These experimental techniques have promised an ultimate quantum control in quantum optical systems. With well control of atomic configurations, we can manipulate RDDI of the spontaneous emission process. This controls the timescale of the emission, which makes subradiant states a resource for quantum memory. Subradiant far-field scattering, on the other hand, provides additional information for light collection and specific characterization of atomic geometry. This helps prepare genuine quantum states and makes quantum state engineering more efficient.
In conclusion, we propose to prepare the multiphoton subradiant states by imprinting the helical phases from OAM of light on the atoms in the stacked and concentric rings, and investigate their far-field scattering patterns. The directional scattering of the helical-phase-imprinted multiphoton subradiant states allows for light collimation, and their small spontaneous decay rates are preferential to quantum storage of light quanta with orbital angular momenta. We find enhanced forward (oblique backward) emission for HPI two (three)-photon subradiant states which can also support transverse scattering peaks. Therefore, we can tailor and control the scattering properties by engineering the atoms spatially, which essentially can facilitate quantum control of the many-body subradiant states and is useful in manipulating entanglement of large orbital angular momenta48 or operating quantum gates49.
Methods
Lindblad form of dissipation with resonant dipole-dipole interactions
The coupling matrix is based on the Lindblad forms of the spontaneous emissions. The general spontaneous emission process involves the dipole-dipole interaction4 which results from the rescattering events in the dissipation. For a quantum operator \(\hat{Q}\), the Heisenberg equation in a Lindblad form reads
where for the spontaneous emission,
The dipole operator is \({\hat{\sigma }}_{\mu }^{-}\) (\({\hat{\sigma }}_{\mu }^{+}\)) where \({\hat{\sigma }}_{\mu }^{-}\) ≡ |g〉 μ 〈e| and \({\hat{\sigma }}_{\mu }^{-}\equiv {({\hat{\sigma }}_{\mu }^{+})}^{\dagger }\). The frequency shift G μν and decay rate F μν are4
where Γ is the single-particle intrinsic decay rate of the excited state, ξ = |k L |r μν , and the interparticle distance r μν = |r μ − r ν |. The above expressions are valid for uniformly polarized excitations of the dipole p.
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Acknowledgements
This work is supported by the Ministry of Science and Technology (MOST), Taiwan, under the Grant No. MOST-106-2112-M-001-005-MY3. H.H.J. is partially supported by a grant from MOST of No. 106-2811-M-001-130, as an assistant research scholar in IOP, Academia Sinica. We are also grateful for the support of NCTS ECP1 (Experimental Collaboration Program) and for stimulating discussions with M.-S. Chang and Y.-C. Chen.
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Jen, H.H. Directional subradiance from helical-phase-imprinted multiphoton states. Sci Rep 8, 7163 (2018). https://doi.org/10.1038/s41598-018-25592-5
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DOI: https://doi.org/10.1038/s41598-018-25592-5
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