Fast electrical modulation of strong near-field interactions between erbium emitters and graphene
Daniel Cano, Alban Ferrier, Karuppasamy Pandian Soundarapandian, Antoine Reserbat‐Plantey, Marion Scarafagio, Alexandre Tallaire, Antoine Seyeux, Philippe Marcus, Hugues de Riedmatten, Philippe Goldner, Frank H. L. Koppens, Klaas‐Jan Tielrooij
Combining the quantum optical properties of single-photon emitters with the strong near-field interactions available in nanophotonic and plasmonic systems is a powerful way of creating quantum manipulation and metrological functionalities. The ability to actively and dynamically modulate emitter-environment interactions is of particular interest in this regard. While thermal, mechanical and optical modulation have been demonstrated, electrical modulation has remained an outstanding challenge. Here we realize fast, all-electrical modulation of the near-field interactions between a nanolayer of erbium emitters and graphene, by in-situ tuning the Fermi energy of graphene. We demonstrate strong interactions with a >1000-fold increased decay rate for ~25% of the emitters, and electrically modulate these interactions with frequencies up to 300 kHz - orders of magnitude faster than the emitter's radiative decay (~100 Hz). This constitutes an enabling platform for integrated quantum technologies, opening routes to quantum entanglement generation by collective plasmon emission or photon emission with controlled waveform.
Combining the quantum optical properties of single-photon emitters with the strong near-field interactions available in nanophotonic and plasmonic systems is a powerful way of creating quantum manipulation and metrological functionalities. The ability to actively and dynamically modulate emitter-environment interactions is of particular interest in this regard. While thermal, mechanical and optical modulation have been demonstrated, electrical modulation has remained an outstanding challenge. Here we realize fast, all-electrical modulation of the near-field interactions between a nanolayer of erbium emitters and graphene, by in-situ tuning the Fermi energy of graphene. We demonstrate strong interactions with a >1000-fold increased decay rate for ~25% of the emitters, and electrically modulate these interactions with frequencies up to 300 kHz - orders of magnitude faster than the emitter's radiative decay (~100 Hz). This constitutes an enabling platform for integrated quantum technologies, opening routes to quantum entanglement generation by collective plasmon emission or photon emission with controlled waveform.
Electrically tunable graphene plasmons are anticipated to enable strong light-matter interactions with resonant quantum emitters. However, plasmon resonances in graphene are typically limited to infrared frequencies, below those of optical excitations in robust quantum light sources and many biologically interesting molecules. Here we propose to utilize near fields generated by the plasmon-assisted nonlinear optical response of nanostructured graphene to resonantly couple with proximal quantum emitters operating in the near infrared. We show that the nonlinear near field produced by a graphene nanodisk can strongly excite and coherently control quantum states in two- and three-level atomic systems when the third harmonic of its plasmon resonance is tuned to a particular electronic transition. In the present scheme, emitter and plasmon resonances are nondegenerate, circumventing strong enhancement of spontaneous emission. We envision potential applications for the proposed nonlinear plasmonic coupling scheme in sensing and temporal quantum control.
Inspired by the remarkable ability of plasmons to boost radiative emission rates, we propose leveraging acoustic graphene plasmons (AGPs) to realize tunable, giant Purcell enhancements for single-photon, entangled-photon, and multipolar quantum emitters. These AGPs are localized inside a cavity defined by a graphene sheet and a metallic nanocube and filled with a dielectric of thickness of a few nanometers and consisting of stacked layers of 2D materials, containing impurities or defects that act as quantum light emitters. Through finite-difference time domain (FDTD) calculations, we show that this geometry can achieve giant Purcell enhancement factors over a large portion of the infrared (IR) spectrum, up to 6 orders of magnitude in the mid-IR and up to 4 orders of magnitude at telecommunications wavelengths, reaching quantum efficiencies of 95\% and 89\%, respectively, with high-mobility graphene. We obtain Purcell enhancement factors for single-photon electric dipole (E1), electric quadrupole (E2), and electric octupole (E3) transitions and two-photon spontaneous emission (2PSE) transitions, of the orders of 104, 107, 109, and 109, respectively, and a quantum efficiency of 79\% for entangled-photon emission with high-mobility graphene at a wavelength of λ=1.55μm. Importantly, AGP mode frequencies depend on the graphene Fermi energy, which can be tuned via electrostatic gating to modulate fluorescence enhancement in real time. As an example, we consider the Purcell enhancement of spontaneous single- and two-photon emissions from an erbium atom inside single-layer (SL) WS2. Our results could be useful for electrically tunable quantum emitter devices with applications in quantum communication and quantum information processing.
A scheme to construct analogical atoms using graphene nanostructures via quantum nonlinearity is proposed. Due to the strong field localization capability of graphene plasmons and the significant intrinsic nonlinearity of graphene, a strong nonlinear optical response can be realized even with single-photon excitation. In this process, the quantum vacuum localized plasmonic mode plays a crucial role in achieving the third-order multi-photon nonlinear effect. The eigenfrequency of the nanostructure can shift by an amount tens of times larger than the decay rate, causing the nanostructure cavity to exhibit atomic-like behaviors. Furthermore, multilevel atoms can be constructed through the interaction of composite graphene nanostructures. The parameters of these atoms can be manipulated by adjusting the nanostructure size, Fermi energy, and other parameters. This research holds significant potential for applications in highly integrated, controllable nanophotonics.
Achieving dynamic and broadband control of superradiance and subradiance at elevated temperatures is central to quantum photonic technologies. Herein, we theoretically investigate near-field photonics combined with adiabatic and non-adiabatic time-varying media—created via temporal modulation of material properties—to dynamically generate and coherently manipulate quantum emission states, including single photons and photon pairs. Distinctively, this cavity-free near-field method operates effectively at practical temperatures (tens of Kelvin), circumventing traditional operational constraints. We initiate this approach by exploiting plasmonically coupled silicon carbide color centers, which are used as quantum emitters (QEs), with relatively long coherence lifetimes, enabling precise quantum state control before temperature-induced dephasing sets in. In particular, a hybrid plasmonic waveguide is used as the light delivery method, where its subdiffracted near-field generates nanoscale heating that effectively tunes the energies of color centers, via phonon occupation, on resonance with the near-field. Furthermore, we employ transparent conducting oxides, such as indium tin oxide, that may achieve significant refractive index modulation on the femto–picosecond timescales. The resulting behavior is that of a photonic time crystal (PTC) or an epsilon-near-zero (ENZ) material response, dependent on modulation times, and characterized by the amplification or increased absorption of light, respectively, where both enhance field localization around the embedded QEs and extend periods of super- or subradiance compared to static conditions. Our methodology significantly simplifies scalable quantum photonic integration, while advancing quantum memories and entanglement capabilities under accessible conditions.
Quantum technologies are widely expected to bring a revolution in communications and information technologies in the coming decade allowing, for example, un-paralleled levels of secure communications. For quantum communication, photonic quantum effects have played a central role, but most photonic solutions and systems based on light-matter interaction also require cryogenic environments. Strong coupling of light and matter at the single emitter level is a fundamental quantum resource offering deterministic energy exchange between single photons and a two-level system, and the possibility to achieve single-photon nonlinearities via the anharmonicity of the Jaynes-Cummings ladder. Until recently, however, the conditions for achieving strong-coupling were most commonly met at cryogenic temperatures such that de-coherence processes are suppressed. As a major step forward, we have recently demonstrated room-temperature strong coupling of single molecules [1] and single quantum dots [2] to ultra-confined light fields in plasmonic resonators at ambient conditions. The fact that strong-coupling conditions may be reached at room temperature is of immense interest because it represents a clear route to a practical implementation and use of quantum behaviour in nanophotonic systems and its application in bio-sensing [3]. The talk will discuss how nanoplasmonics can be an enabler of ultrafast room-temperature quantum nanophotonic networks via strong coupling and ultrafast quantum dynamics [4]. We will highlight the physics associated with recently demonstrated room-temperature strong coupling of single molecules in a plasmonic nano-cavity [1] and near-field generated strong coupling of single quantum dots [2] and single quantum emitter Dicke enhancement [5] paving the road towards single-photon quantum nonlinearities. The presentation will also explain near-field enhanced single-photon emission in near-zero index materials [6] and ultrafast multi-partite quantum entanglement [7]. This provides the foundation for unprecedented control over photon number, single photon dynamics, and dynamic multi-photon coherence. These properties are all imperative for the development of next-generation, nanoscale building blocks in ambient-temperature photonic quantum communication technologies.
The spontaneous emission of a V-type three-level quantum emitter near graphene layers is investigated. With appropriate doping densities, graphene layers support transverse electric- (TE-) polarized surface plasmons. This kind of plasmon can enhance the decay rates of dipoles parallel to the layers, and subsequently, strong quantum interference presents between the two orthogonal transition dipoles of the emitter. As a result, the emission field polarization and the spectrum can be radically changed. This can be evidence of the TE-polarized surface plasmons in the graphene layers.