윤태현 교수
Yoon, Tai Hyun
고려대학교 물리학과 · 물리·천문학
연구실 소개
윤태현 교수의 연구실은 광학적 비선형 현상과 초단시간 레이저를 활용한 원자 및 분자의 동적 거동을 정밀하게 분석하는 데 초점을 맞추고 있습니다. 특히 레이저 유도 이방성, 이중 주파수 콤 기반 초고속 투과 측정, 그리고 양자 간섭 현상을 이용한 파동-입자 이중성의 정량적 분석 등 고해상도 및 고속 측정 기법을 개발하고 있습니다. 이와 함께 냉각된 원자 시스템과 광학적 간섭을 기반으로 한 고정밀 나노메트로로지 기술도 함께 연구하고 있습니다.
연구 현황
연구 성과 추이
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주요 논문
15We report the observation of laser-induced birefringence (LIB) in a wavelength-mismatched cascade system ($J=0\ensuremath{\leftrightarrow}J=1\ensuremath{\leftrightarrow}J=0$ transitions) of inhomogeneously broadened ytterbium atoms with strong pump and probe fields. We investigate the transmission spectrum of two circular polarization (${\ensuremath{\sigma}}_{p}^{+}$ and ${\ensuremath{\sigma}}_{p}^{\ensuremath{-}}$) components of strong probe field at fixed frequency, depending on the detuning o
between the quantons and the remaining degrees of freedom by the relation [Formula: see text], which is experimentally confirmed. We further prove that the experimental scheme using two stimulated parametric downconversion processes is an ideal tool for investigating and understanding wave-particle duality and Bohr's complementarity quantitatively.
A two-photon transition in cold Rb atoms will be probed with a phase-coherent wide bandwidth femtosecond laser comb. Frequency domain analysis yields a high-resolution picture where phase coherence among various transition pathways through different intermediate states produces interference effects on the resonantly enhanced transition probability. This result is supported by the time domain Ramsey interference effect. The two-photon transition spectrum is analyzed in terms of the pulse repetiti
We experimentally demonstrate a dual-frequency comb-based transient absorption (DFC-TA) technique, which has a 12 fs time resolution and an ultrafast scan rate. Here, the fast scan rate is achieved by employing asynchronous optical sampling (ASOPS), which utilizes two independent mode-locked lasers with a slightly detuned repetition rates. The ASOPS approach is advantageous because photodegradation damage of optical sample during TA measurements can be minimized by a gated sampling. We show that
We propose one- and two-wavelength methods of absolute measurement of diffraction-grating spacings based on the Littman configuration for autocollimation. The one-wavelength method has been applied to measure the spacing of a grating with a nominal value of 2160grooves/mm . The grating spacing was measured to be 463.16 nm, with an experimental standard deviation of 0.24 nm. It has been demonstrated that the both methods can provide direct traceability in the submicrometer region in terms of wave
A numerical method is introduced that solves the optical Bloch equations describing a two-level atom interacting with a strong polychromatic pump field with an equidistant spectrum and an arbitrarily intense monochromatic probe field. The method involves a transformation of the optical Bloch equations into a system of equations with time-independent coefficients at steady state via double harmonic expansion of the density-matrix elements, which is then solved by the method of matrix inversion. T
We demonstrate that a dual frequency comb-transient absorption (DFC-TA) technique can be combined with a time-domain interferometric detection to measure both the transient absorption and refraction spectra of molecules in solution. To do this, the pump-probe signal field of DFC-TA is allowed to interfere with a time-delayed local oscillator field in a time domain. We show that this DFC interferometric pump-probe spectroscopy (DFC-IPS) technique has a unique ability to extract the phase and ampl
Analytic solutions of the optical Bloch equations for a two-level atom interacting with a strong polychromatic field whose frequencies are symmetrically positioned with respect to the atomic frequency are used to obtain the polarization spectrum of the atom. The spectrum is found to consist of a series of discrete peaks or dips superimposed on the continuous part of the spectrum. Physical interpretation of resonances exhibited in the continuous part of the spectrum is given using a semiclassical
A complete understanding of a photochemical reaction dynamics begins with real-time measurements of both electronic and vibrational structures of photoexcited molecules. Time-resolved impulsive stimulated Raman spectroscopy (TR-ISRS) with femtosecond actinic pump, Raman pump, and Raman probe pulses is one of the incisive techniques enabling one to investigate the structural changes of photoexcited molecules. Herein, we demonstrate that such femtosecond TR-ISRS is feasible with synchronized tripl
We present an environmentally-stable picosecond Yb-doped fiber laser by employing an achromatic quarter-wave-plate (AQWP) as a pulse stabilizer in the all-normal-dispersion and polarization-maintaining linear laser cavity. It is shown that the AQWP plays a critical role to control both the polarization state and spectral filtering of the proposed mode-locked laser. The demonstrated laser generates 2-ps-long pulses with pulse energies of 1 nJ at a repetition rate of 117 MHz and parabolic spectral
Tellurium (Te) microcrystal with a bandgap of approximately 0.37 eV is a potentially useful semiconducting material exhibiting ultrafast electronic relaxation processes. To measure the intervalley and intravalley relaxation rates, we carried out two-color near-IR (NIR) pump and mid-IR (MIR) probe studies of rod-type Te microcrystals, employing a repetition-frequency-stabilized NIR (800 nm) laser and an MIR (3300 nm) frequency comb. Using interferometrically detected two-color asynchronous sampli
By employing two synchronized mode-locked femtosecond lasers and interferometric detection of the pump-probe spectra—referred to as asynchronous and interferometric transient absorption—we have developed a method for broad dynamic range and rapid data acquisition. Using asynchronous and interferometric transient absorption, we examined photochemical changes during femtosecond pump-probe experiments on all-inorganic cesium lead halide nanomaterials. The laser pulse train facilitates photoreaction
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