No abstract

The absorption of traveling photons resonant with electric dipole transitions of an atomic gas naturally leads to electric dipole spin wave excitations. For a number of applications, it would be highly desirable to shape and coherently control the spatial waveform of the spin waves before spontaneous emission can occur. This work details a recently developed optical control technique to achieve this goal, where counter-propagating, shaped sub-nanosecond pulses impart sub-wavelength geometric phases to the spin waves by cyclically driving an auxiliary transition. In particular, we apply this technique to reversibly shift the wave vector of a spin wave on the D2 line of laser-cooled 87 Rb atoms, by driving an auxiliary D1 transition with shape-optimized pulses, so as to shut off and recall superradiance on demand. We investigate a spin-dependent momentum transfer during the spin-wave control process, which leads to a transient optical force as large as ∼ 1 k/ns, and study the limitations to the achieved 70 ∼ 75% spin wave control efficiency by jointly characterizing the spin-wave control and matterwave acceleration. Aided by numerical modeling, we project potential future improvements of the control fidelity to 99% level when the atomic states are better prepared and by equipping a faster and more powerful pulse shaper. Our technique also enables a backgroundfree measurement of the superradiant emission to unveil the precise scaling of the emission intensity and decay rate with optical depth for the first time to our knowledge.

Advances of quantum control technology have led to nearly perfect single-qubit control of nuclear spins and atomic hyperfine ground states. In contrast, quantum control of strong optical transitions, even for free atoms, are far from being perfect. Developments of such quantum control appears to be limited by available laser technology for generating isolated, sub-nanosecond optical waveforms with 10's of GHz programming bandwidth. Here we propose a simple and robust method for the desired pulse shaping, based on precisely stacking multiple delayed picosecond pulses. Our proof-of-principal demonstration leads to arbitrarily shapeable optical waveforms with 30 GHz bandwidth and 100 ps duration. We confirm the stability of the waveforms by interfacing the pulses with laser-cooled atoms, resulting in “super-resolved” spectroscopic signals. This pulse shaping method may open exciting perspectives in quantum optics, and for fast laser cooling and atom interferometry with mode-locked lasers.

Parvovirus B19 (B19V) is pathogenic to humans and causes various human diseases. However, no antiviral agents or vaccines currently exist for the treatment or prevention of B19V infection. Therefore, developing sensitive and specific methods for B19V infection diagnosis is essential for accurate diagnoses. Previously, a Clustered Regularly Interspaced Palindromic Repeats (CRISPR)-Cas12a (cpf1)-based electrochemical biosensor (E-CRISPR) with a picomole sensitivity for B19V detection was established. Herein, we set up a novel nucleic acid detection system based on Pyrococcus furiosus Argonaute (PfAgo)-mediated nucleic acid detection, targeting the nonstructural protein 1 (NS1) region of the B19V viral genome (abbreviated B19-NS1 PAND). Benefiting from independent protospacer adjacent motif (PAM) sequences, PfAgo can recognize their target with guide DNA (gDNA) that is easy to design and synthesize at a low cost. In contrast to E-CRISPR, without preamplification with Polymerase Chain Reaction (PCR), the Minimum Detectable Concentration (MDC) of three guide- or single guide-mediated B19-NS1 PAND was about 4 nM, approximately 6-fold more than E-CRISPR. However, when introducing an amplification step, the MDC can be dramatically decreased to the aM level (54 aM). In addition, the diagnostic results from clinical samples with B19-NS1 PAND revealed 100% consistency with PCR assays and subsequent Sanger sequencing tests, which may assist in molecular testing for clinical diagnosis and epidemiological investigations of B19V.

The propagation of light in moving media is dragged by atomic motion. The light-drag effect can be dramatically enhanced by reducing the group velocity with electro-magnetically induced transparency. We demonstrate a systematic procedure to estimate the velocity field of the moving atoms, by holographically reconstructing the complex wavefront of the slow light and to simultaneously retrieve the absorption and phase shift. This large-NA, photon-shot-noise-limited inline coherent imaging technique may assist a wide range of cold atom experiments to access phase space information with in situ and minimally destructive measurements. By faithfully expanding the imaging data from real to complex numbers, the holographic technique also paves a way toward single shot spectroscopic imaging of atomic ensembles, even in presence of atomic density fluctuations.