SearcharxivSearch

arXiv · 2511.23462

Arbitrary control of the temporal waveform of photons during spontaneous emission

Abstract

Control of the temporal waveform of photons produced during spontaneous emission from single quantum emitters provides a crucial tool in the establishment of hybrid quantum systems, optimization of quantum state transfer protocols and mitigation of effects due interferometric instability for network architectures based on flying qubits. We describe a method to generate photons of any temporal waveform from emitters of any excited state lifetime, limited only by the timing resolution of control hardware. We show how the temporal waveform of photons can be controlled by deterministically varying the population of an excited state which undergoes spontaneous emission. Our broadly applicable approach has only two requirements for a candidate quantum emitter: modulation of the (1) amplitude and (2) relative phase of a field coupling a ground state to the excited manifold. We detail how to identify optimal excitation pulses by employing variational algorithms to feed back on atomic populations. Additionally, we develop Quantum Monte Carlo based tools to determine photon-number statistics and establish techniques to identify optimal excitation strengths and post-selection thresholds for photon generation protocols. We situate our work in the context of other prior research on bespoke single photon sources and networking including post-emission pulse shaping, temporal gating and cavity-based methods. In comparison, our free-space process has greater flexibility in producing any waveform, requires less infrastructure, and can be readily applied across a wide range of quantum emitters. We discuss the applications and limits of this technique, including how increasing photon emission probabilities affects achievable temporal-mode overlap fidelities between emitted and target photon waveforms.

Explore related subjects

Keep this discovery

BibTeXRIS

Carl Thomas, Rebecca Munk, Boris Blinov. 2025-11-28. Arbitrary control of the temporal waveform of photons during spontaneous emission. https://doi.org/10.1103/t18q-5ls4

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Delay-engineered dynamical phases in a programmable non-Markovian spin oscillator

Non-Markovian dynamics offer a new route towards engineering non-equilibrium matter, where memory and feedback act as programmable resources for controlling order in time. Here we report the realization of a non-Markovian spin oscillator in a hot vapour $^{129}$Xe-Cs co-magnetometer with programmable feedback delay and gain. By tuning these parameters, we observe a hierarchy of dynamical phases, including time-crystalline response, nonlinear bifurcations, and frequency-comb formation. The measured spectra and phase boundaries are captured by linear stability analysis of delayed Bloch equations, revealing these phenomena as different manifestations of the same memory-induced instability structure. These results establish time-delayed feedback as a powerful strategy for controlling non-equilibrium phases, enabling quantum sensing, frequency referencing, and synchronization within a single spin-based platform.

physics.atom-ph

Non-stick vacuum wall collisions with a laser-coolable molecule

Molecular species that are suitable for direct laser cooling are typically considered lost or destroyed if they collide with an ambient temperature vacuum wall. Here, we study surface collisions with aluminum monofluoride (AlF), a laser-coolable molecule that survives this process with unusually high probability. We detect the outgoing AlF molecules from a single wall collision via Doppler-sensitive laser-induced fluorescence spectroscopy, using incoming supersonic (pulsed) and thermochemical (continuous) molecular beams. The angular, velocity and rovibrational level distributions of the outgoing molecules show near-complete thermalisation to the wall in a single collision event. We determine an upper limit to the surface residence time of about 5$~\mu$s, and by monitoring the decay in density of pulses of molecules loaded into a small storage volume, we deduce the surface sticking probability for different materials. For a siloxane-coated metallic surface, the sticking probability of AlF is about 0.015, allowing us to accumulate molecules from the thermochemical source into an ambient temperature storage vessel at densities near $10^{8}~$cm$^{-3}$. This provides a route to compact, portable traps for neutral molecules.

physics.atom-ph

Kinetic modeling of molecular beam formation in a cryogenic buffer-gas cell

Cryogenic buffer-gas cells are widely used to produce cold molecular beams, but the microscopic dynamics governing beam formation remain challenging to model. Here we present fully kinetic simulations of a cryogenic buffer-gas cell using the Direct Simulation Monte Carlo method implemented in the PICLas framework, treating the buffer gas and ablated molecules within a single unified model. We capture characteristic features of cryogenic buffer-gas sources, including plume cooling, directed transport toward the aperture, and the formation of a slow molecular beam, while also resolving energy transfer from the hot ablation plume to the helium buffer gas that is inaccessible to existing approaches relying on the background-gas approximation. Our results demonstrate that fully kinetic simulations can provide detailed insights into buffer-gas cell dynamics and open a route toward a systematic optimization of such sources.

physics.atom-ph