双折射光子晶体光纤中基于孤子分裂的超连续光谱产生

利用亚纳焦量级、脉冲宽度为100 fs的激光脉冲在双折射光子晶体光纤中获得了450—1050 nm 的超连续光谱,且超连续光谱具有明显的分立峰状结构.分析了光谱中分立峰状结构产生的物理机制,抽运光波长处于接近零色散波长的反常色散区,形成高阶光孤子,由于高阶非线性和高阶色散的影响,高阶孤子分裂成多个基孤子,使初始光谱上演化出红移的光孤子成分和蓝移的色散波成分.理论模拟了飞秒激光脉冲在光纤中的色散特性和传输特性,较好地解释了实验结果. 关键词： 光子晶体光纤 超连续光谱产生 孤子分裂 脉冲俘获     

1040nm泵浦的光子晶体光纤超连续光谱产生性能退化研究

光子晶体光纤已经被广泛应用于由飞秒脉冲激光源产生超连续光谱。当激光源的重复频率较低时,由光子晶体光纤产生的超连续光谱随时间的变化过程较为缓慢,通常不被注意到。而在天文光谱仪定标等应用中,需要使用GHz至几十GHz量级的高重复频率激光源。此时,可观察到光子晶体光纤的超连续光谱产生性能在有限时间内产生显著的退化。在1 040 nm飞秒激光泵浦条件下,通过测试三种不同气孔占空比的光子晶体光纤的超连续光谱产生性能演化,发现超连续光谱的退化进程随光纤气孔占空比的增大而加速。观察发生光谱退化后的光子晶体光纤样品,发现在光纤上超连续光被产生的区段出现多个不同颜色的亮点,呈现有方向性的光泄露现象。针对光泄露现象,通过测量光纤的吸收光谱线,证实了实验中超连续光谱退化的主因并非是光纤熔融石英材料中大量非桥氧色心产生。针对光泄露具有方向性这一特征,提出了经由多光子吸收作用在光纤纤芯中形成长周期光栅的理论。为探究影响光子晶体光纤超连续光谱产生性能的退化的因素,以达到光谱退化抑制的目的,首先通过改变了光纤的拉锥参数,期望增强光纤熔融石英材料的光子耐受性。实验结果证实了该方法的有效性较为有限。其次,从保持激光源的平均功率,降低激光脉冲的峰值功率和保持激光脉冲的峰值功率,降低激光源平均功率两个方面入手,对激光源进行调制。实验结果证明,光纤单位时间内接受的高峰值功率脉冲总量是影响其超连续光谱产生性能的最重要因素。在天文光谱仪定标的应用中,对超连续光谱光功率的需求并不高,使用斩波器降低光子晶体光纤入射光的平均功率是减缓超连续光谱产生性能退化过程的有效且简单可行的方法。     

全光纤高效超连续谱光源实验研究

 报道了一个全光纤的高效率超连续谱产生系统,系统采用增加一段匹配光纤的办法解决增益光纤和光子晶体光纤直接熔接损耗较大的问题,并且对匹配光纤和光子晶体光纤熔接对准过程进行实时监控,使熔接损耗降到最低,从而实现了较高的全系统转换效率(76%)和较好的光束质量。实验研究了超连续光谱展宽的过程,结果显示：超连续谱展宽的初始阶段,拉曼效应和自相位调制效应起主要作用,光谱呈现长波方向展宽较多的非对称性,并出现明显的拉曼斯托克斯峰;光谱继续展宽时,满足相位匹配条件的四波混频开始起作用,拉曼效应产生的加宽光谱成分作为四波混频参量过程的泵浦,使光谱开始向长波和短波两个方向扩展。     

孤子光脉冲的产生及其应用研究

利用非线性偏振旋转技术实现自起振被动锁模.在掺铒光纤环形腔激光器中产生了中心波长为1563.3 nm、重复频率为12.5 MHz、脉冲宽度为352.0 fs、3 dB光谱宽度为7.8 nm的孤子光脉冲.采用该孤子光脉冲作为抽运光源，经掺铒光纤放大器放大后，输入到101 m长的高非线性光子晶体光纤中，获得了20 dB带宽约为240 nm的超连续激光光谱.实验详细观测了光脉冲随抽运功率的变化及超连续激光光谱的形成过程，分析了其形成机理.研究表明：当抽运功率较低时，光谱加宽主要由高阶孤子的分裂引起；随着抽运功率的增加，高阶孤子分裂成基本孤子的数目逐渐增大，光谱进一步加宽；当抽运功率增加到受激拉曼散射的阈值时，受激拉曼散射成为光谱展宽的主要原因；抽运功率进一步增加时，受激拉曼散射、参量四波混频等非线性的共同作用将使光谱进一步加宽且变得光滑. 关键词： 孤子光纤激光器 超连续 光子晶体光纤     

百飞秒级脉宽的宽带超连续谱光源的产生

实现了一种适合于相干拉曼光谱探测的宽带超连续谱光源的方法,使用1 064nm飞秒激光泵浦全正色散光子晶体光纤,并用光栅对对脉冲进行压缩,最终获得了脉宽178fs,频谱范围处于760～1 300nm的超连续谱光源.对超连续谱脉冲的时间频谱结构进行了分析,未经过压缩的超连续谱的脉冲宽度达到1.43ps,不同频率的成分之间延迟较大,但基本上呈线性平滑分布,因此可以使用光栅对进行色散补偿;此外,提高泵浦光的功率虽然能够增加光谱展宽,但会引入高阶色散,并不利于色散补偿.最后,使用该超连续谱搭建的三色相干反斯托克斯拉曼散射光谱探测系统,测量了苯甲腈溶液的相干反斯托克斯拉曼散射信号光谱,同时获得了3 200cm~(-1)范围内的所有振动模式,验证了该超连续光谱的性能.     

飞秒激光在光子晶体光纤中产生超连续光谱机制的实验研究

报道了利用零色散在780nm处的光子晶体光纤与纳焦耳量级的飞秒激光脉冲相互作用的实验结果.实验使用35fs，中心波长810—840nm，单脉冲能量可达14nJ的飞秒激光光源获得了超过一个倍频程的平坦超连续光谱（500—1100nm）.在不同功率、不同中心波长、不同啁啾和有无直流成分的多种飞秒脉冲激光的条件下，研究了超连续光谱的产生情况.并对一系列现象进行了对比，分析了超连续光谱产生的机制. 关键词： 光子晶体光纤 飞秒脉冲激光 超连续光谱     

高非线性光子晶体光纤中飞秒脉冲的传输特性和超连续谱产生机制的实验研究及模拟分析

用实验和数值模拟两种方法研究了高非线性光子晶体光纤中飞秒激光脉冲的传输特性和超连续谱的产生机理，给出了抽运脉冲在三种不同中心波长情况下输出光谱展宽并形成超连续谱的实际测量及理论模拟结果.研究表明：在零色散波长抽运时，光谱展宽以自相位调制为主，同时三阶色散的影响明显，传输脉冲在时域内出现振荡次峰.而在反常色散区抽运时，光谱展宽的初期以自相位调制为主，随后根据抽运功率的不同孤子自频移、高阶光孤子的裂变和四波混频效应会逐渐增强，进而成为光谱展宽的主要原因.与此相应，在时域中能明显看到孤子的形成和红移，飞秒传输脉 关键词： 光子晶体光纤 高非线性光子晶体光纤 飞秒脉冲激光 超连续谱     

基于预啁啾控制的极宽带光参量放大

在以飞秒钛宝石放大系统的倍频光为抽运光和超连续白光为信号光的光参量放大中,针对抽运光的宽带特点,分析了一种新的极宽带相位匹配方法.结果表明,10nm的抽运光带宽可得到近400nm的相位匹配带宽,若抽运光带宽达到20nm,相位匹配带宽就能达到近600nm.零色散波长为800nm的光子晶体光纤产生的超连续谱经光纤传输后为二次啁啾,宽带抽运光经棱镜对展宽具有线性啁啾,满足了极宽带相位匹配方法所需要的光谱分布.理论计算了对输入脉冲进行预啁啾控制应选择的光纤长度和棱镜对在光路中的插入量,为实现极宽带光参量放大提供了 关键词： 啁啾 极宽带相位匹配 光参量放大 光子晶体光纤     

飞秒钛宝石激光脉冲的载波包络相移测量研究

飞秒激光脉冲的载波包络相移测量与控制是实现阿秒脉冲与光学原子钟的重要内容，在利用光子晶体光纤扩展飞秒钛宝石激光振荡器光谱的研究基础上，通过自参考技术测量并优化了该激光输出脉冲的载波包络相移所引起的拍频信号.实验上采用半导体抽运的倍频Nd:YVO4532nm激光器作为抽运源，对钛宝石激光器所产生的平均功率500mW、脉宽18fs的光脉冲进行拍频测量后观察到约23MHz的频移，对应于每周期053π的载波包络相移.飞秒激光脉冲载波包络相移测量的实现对于进一步利用电子反馈系统精确控制载波包络相移，从而得到高稳定的飞秒激光频率梳具有重要意义. 关键词： 载波包络相移 光子晶体光纤 飞秒 超连续     

国产光子晶体光纤实现4.6W全光纤超连续谱输出

采用自行搭建的被动锁模皮秒脉冲掺镱光纤激光器作为抽运源,将其输出尾纤与国产光子晶体光纤(PCF)进行低损耗熔接,构成全光纤结构的高功率超连续谱(SC)光源。全光纤结构提高了超连续谱产生系统的稳定性和转换效率。实验观察了皮秒脉冲在正常色散区抽运光子晶体光纤产生超连续谱过程,并对超连续谱的产生机理进行了理论解释。该光源输出平均功率为4.6W的超连续谱,超连续光谱展宽超过1000nm,光光转换效率为54%。     

Tunable light source for coherent anti-Stokes Raman scattering microspectroscopy based on the soliton self-frequency shift

We present a photonic crystal fiber (PCF)-based light source for generating tunable excitation pulses (pump and Stokes) that are applicable to coherent anti-Stokes Raman scattering (CARS) microspectroscopy. The laser employed is an unamplified Ti:sapphire femtosecond laser oscillator. The CARS pump pulse is generated by spectral compression of a laser pulse in a PCF. The Stokes pulse is generated by redshifting a laser pulse in a PCF through the soliton self-frequency shift. This setup allows for probing up to 4000 cm(-1) with a spectral resolution of approximately 25 cm(-1). We characterize the stability and robustness of CARS microspectroscopy employing this light source.     

Supercontinuum generated in all-normal dispersion photonic crystal fibers with picosecond pump pulses

The supercontinuum (SC) generation in all-normal dispersion (ANDi) photonic-crystal fiber (PCF) pumped by high power picosecond pulses are investigated in this paper. Our results show that an octave SC may be achieved by pumping the ANDi PCF with picosecond pump pulses. However, the PCF length required may have to be lengthened to several tens of centimeters, which is much longer than that with femtosecond pump pulses. The relatively long PCF gives rise to much higher Raman gain and stronger Raman frequency shift compared to those with femtosecond pump pulses, which in turn not only cause a distorted temporal waveform and an un-flattened spectrum, but also severely degrade the coherence of the generated SC.     

光子晶体光纤产生飞秒超连续谱的实验研究

研究了飞秒脉冲经过光子晶体光纤时超连续谱产生的物理机制。采用输出波长可调谐的钛宝石光参量放大器作为泵浦源,光纤光谱仪测量不同泵浦功率和不同泵浦波长条件下光子晶体光纤产生的超连续谱的光谱图,对进行了归一化处理后的不同泵浦功率和不同泵浦波长条件下的超连续谱进行对比,分析影响光子晶体光纤超连续谱差异的物理机制。实验结果表明,当泵浦波长不变时,随着入射泵浦脉冲平均功率的增大,波峰增多,谱宽也逐渐加宽并伴随着出现能量向短波方向集中的现象,泵浦功率到达一定强度时,超连续谱的宽度最后到达饱和,谱的包络趋于稳定;入射光功率稳定在300 mW时,超连续谱的宽度和形状皆受到泵浦波长影响,在760～840 nm范围内,泵浦波长越长,波峰数越多,泵浦脉冲波长离零色散点越近,光子晶体光纤产生的超连续谱谱宽会越宽,超连续谱的形状相对越平坦。     

Coherent anti-Stokes Raman scattering and normal anti-Stokes Raman scattering due to LO phonons in GaP using cw diode lasers

Coherent anti-Stokes Raman scattering (CARS) and normal anti-Stokes Raman scattering (NARS) have been measured in (001) GaP at room temperature due to the 403 cm⁻¹ LO phonons using a continuous wave (CW) 785.0 nm fixed-wavelength pump laser and a CW Stokes laser tunable in the 800-830 nm wavelength range. CARS measurements are normally made using pulsed lasers. The use of CW diode lasers allows a more accurate comparison between the measured and calculated values of the CARS signal. The pump and Stokes laser beams were linearly polarized perpendicular to each other, same as the pump and normal Stokes/anti-Stokes scattered light for the GaP sample used in this work. The pump and Stokes laser powers incident upon the GaP sample, located in the focal plane of a 20 mm effective focal length lens, were <20 and 50 mW, respectively. The diameter of the laser beams in the focal plane of the focusing lens was determined to 40±5 μm. The pump and Stokes laser beam intensities incident upon the 0.3 mm thick GaP sample were <2 and 5 kW cm², respectively. The powers of the CARS and NARS signals were measured using a Raman spectrometer. The signal output of the Raman spectrometer was calibrated using the pump laser and several neutral density filters. The Raman linewidth (full-width at half-maximum) of the LO phonons was determined to be 0.95±0.05 cm⁻¹, using the variation of the CARS signal with the wavelength of the Stokes laser. The measured powers of the CARS and NARS signals are about a factor of 5 and 1.5, respectively, smaller than those calculated from the corresponding theoretical expressions.     

Selective excitation and suppression of coherent anti-Stokes Raman scattering by shaping femtosecond pulses

Femtosecond coherent anti-Stokes Raman scattering (CARS) suffers from poor selectivity between neighbouring Raman levels due to the large bandwidth of the femtosecond pulses. This paper provides a new method to realize the selective excitation and suppression of femtosecond CARS by manipulating both the probe and pump (or Stokes) spectra. These theoretical results indicate that the CARS signals between neighbouring Raman levels are differentiated from their indistinguishable femtosecond CARS spectra by tailoring the probe spectrum, and then their selective excitation and suppression can be realized by supplementally manipulating the pump (or Stokes) spectrum with the $\pi $ spectral phase step.     

Two-photon absorption-induced effects in femtosecond coherent anti-Stokes Raman-scattering microspectroscopy of silicon photonic components

We study the effects related to two-photon absorption (TPA) in the microspectroscopy of the silicon photonic components based on coherent anti-Stokes Raman scattering (CARS) of femtosecond pulses. With 300-fs pulses of 1.24-μm Cr:forsterite laser radiation delivering pump and probe fields and a frequency-shifted soliton output of a large-mode area photonic-crystal fiber employed as a Stokes field, pronounced TPA effects have been observed in the CARS microspectroscopy of silicon components for pump-pulse intensities exceeding 10 GW/cm².     

Build-up of supercontinuum in heated and unheated photonic crystal fibers using a chirped femtosecond laser

The build-up of supercontinuum in a photonic crystal fiber (PCF) has been investigated experimentally as a function of pump power using chirped 100-fs pulses from a Ti:sapphire laser. As compared with the PCF at room temperature, a new blue-shifted spectral component is observed in the initial steps of supercontinuum (SC) generation when the central part of PCF is heated to 120 °C by a hot plate. In addition, the slope efficiency of SG is slightly improved with the slightly extension of supercontinuum spectrum in blue edge at high pump powers. The change in dispersion property as well as the effective cascading of nonlinear photonic crystal fibers for heated PCF would be the main attributions.     

High energy femtosecond supercontinuum light generation in large mode area photonic crystal fiber

A large mode area photonic crystal fiber (LMA PCF) with an effective area of 180 μm² is used to generate a high energy, micro-joule range, flat, octave spanning supercontinuum (SC) extending from ~ 600 nm to ~ 1720 nm. A train of femtosecond pulses from a widely-tunable parametric amplifier pumped by a Ti:Sapphire regenerative amplifier system are coupled into a 20 cm length of LMA PCF generating a SC of 1.4 μJ energy. We present an experimental study of the high energy SC as a function of the input power and the pumping wavelength. The spectrum obtained at a pump wavelength of 1260 nm presents spectral flatness variation less than 12 dB over more than 1.1 octave bandwidth. The physical processes behind the SC formation are described in the normal and the anomalous dispersion regions. Our experimental results are successfully compared with the numerical solution of the nonlinear Schrödinger equation.     

20 W all fiber supercontinuum generation from picosecond MOPA pumped photonic crystal fiber

An all fiber high power supercontinuum (SC) source is demonstrated by pumping a section of photonic crystal fiber (PCF) with a picosecond MOPA laser. The core of the PCF is enlarged at the input end through a serious of PCF post processing method to match the output fiber of the picosecond laser, to ensure low loss splicing, hence high power operation of the whole system. The supercontinuum output spectrum covers the wavelength range from 650 nm to beyond 1700 nm. Limited by available pump power, 20 W super-continuum output power is obtained under 29.5 W picosecond pump power, giving a high optical to optical conversion efficiency of 67.8%.     

Polarization‐resolved high‐resolution Raman spectroscopy with a light‐emitting diode

We demonstrate the use of a light‐emitting diode (LED) based experimental setup for collecting polarization‐resolved Raman spectra with good spectral resolution. The combination of a commercial red LED (630 nm), a 1‐nm bandwidth laser‐line filter, and a polarizing prism is used as a light source. Polarization‐resolved spectra in dimethyl sulfoxide are recorded and compared with the corresponding laser‐Raman spectra. The LED‐excited spectra exhibit a resolution slightly lower than those in the laser case but still close to the resolution of the spectrometer. All relevant spectral features of dimethyl sulfoxide including the symmetric and antisymmetric stretching modes of the CSC moiety are resolved with the experimental setup providing a spectral resolution of approximately 20 cm⁻¹. Copyright © 2013 John Wiley & Sons, Ltd.