Quantum optical coherence tomography

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Quantum optical coherence tomography (Q-OCT) is an imaging technique that uses nonclassical (quantum) light sources to generate high-resolution images based on the Hong-Ou-Mandel effect (HOM).[1] Q-OCT is similar to conventional OCT but uses a fourth-order interferometer that incorporates two photodetectors rather than a second-order interferometer with a single photodetector.[2] The primary advantage of Q-OCT over OCT is insensitivity to even-order dispersion in multi-layered and scattering media.[3][4][5]

Several quantum sources of light have been developed so far. An example of such nonclassical sources is spontaneous parametric down-conversion that generates entangled photon pairs (twin-photon).[6] The entangled photons are emitted in pairs and have stronger-than-classical temporal and spatial correlations. The entangled photons are anti-correlated in frequencies and directions. However, the nonclassical light sources are expensive and limited, several quantum-mimetic light sources are developed by classical light and nonlinear optics, which mimic dispersion cancellation and unique additional benefits.[7]

Theory

The principle of Q-OCT is fourth-order interferometry. The optical setup is based on a Hong ou Mandel (HOM) interferometer with a nonclassical light source. Twin photons travel into and recombined from reference and sample arm and the coincidence rate is measured with time delay.[8]

Hong-Ou-Mandel interferometer
Hong-Ou-Mandel interferometer

The nonlinear crystal is pumped by a laser and generates photon pairs with anti-correlation in frequency. One photon travels through the sample and the other through a delay time before the interferometer. The photon-coincidence rate at the output ports of the beam splitter is measure as a function of length difference (cτq) by a pair of single-photon-counting detectors and a coincidence counter.

Due to the quantum destructive interference, both photons emerge from the same port when the optical path lengths are equal. The coincidence rate has a sharp dip when the optical path length difference is zero. Such dips are used to monitor the reflectance of the sample as a function of depth.[9]

The twin-photon source is characterized by the frequency-entangled state:

|ψ=dΩζ(Ω)|ω0+Ω1|ω0Ω2,

where Ω is the angular frequency deviation about the central angular frequency ω0 of the twin-photon wave packet, ζ(Ω) is the spectral probability amplitude.

A reflecting sample is described by a transfer function:

H(ω)=0dzr(z,ω)ei2ϕ(z,ω),

where H(ω)=r(z,ω) is the complex reflection coefficient from depth z,

The coincidence rate C(τq) is then given by

A-scan plot of the quantum optical coherence tomography
A-scan plot of the quantum optical coherence tomography

C(τq)Λ0ReΛ(2τq),

where

Λ0=dΩ|H(ω0+Ω)|2S(Ω),

and

Λ(τq)=dΩH(ω0+Ω)H(ω0Ω)S(Ω)eiΩτq,

represent the constant (self-interference) and varying contributions (cross-interference).[10]

Dips in the coincidence rate plot arise from reflections from each of the two surfaces. When two photons have equal overall path lengths, the destructive interference of the two photon-pair probability amplitude occurs.

Advantages

Compared with conventional OCT, Q-OCT has several advantages:

  • greater signal-to-background ratio;[11]
  • intrinsic resolution enhancement by a factor of two for the same source bandwidth;[12]
  • interferogram components that are insensitive to even-order dispersion of the medium;[13]
  • interferogram components that are sensitive to the dispersion of the medium[14]

Applications

Similar to FD-OCT, Q-OCT can provide 3D imaging of biological samples with a better resolution due to the photon entanglement.[15] Q-OCT permits a direct determination of the group-velocity dispersion (GVD) coefficients of the media.[16] The development of quantum-mimetic light sources offers unique additional benefits to quantum imaging, such as enhanced signal-to-noise ratio, better resolution, and acquisition rate. Although Q-OCT is not expected to replace OCT, it does offer some advantages as a biological imaging paradigm.

References

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