833 resultados para Fiber lasers


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报道了一个相位锁定的光纤激光器阵列获得60W的输出,同相模式输出时的斜率效率为37%。对于两种不同的纤芯距离都观测到稳定的高对比度干涉条纹。整个系统在高功率操作时,所用的空间滤波器没有观察到明显的热问题,这充分说明了采用这种方法能够进一步提高相干输出功率。

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对高功率脉冲双包层光纤激光器的国内外研究进展进行评述,通过建立了小信号瞬态增益模型,对脉冲激光信号经过双包层光纤放大后的波形进行了数值模拟。分析了基于MOPA方式脉冲双包层光纤激光器的几个问题,报道了中科院上海光机所采用振荡-放大(MOPA)方法获得133.8W平均功率脉冲放大输出的实验结果。

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利用一个自成像共焦腔和一个空间滤波器实现了两掺Yb大芯光纤激光器的位相锁定。观测到稳定的具有高对比度的干涉条纹。相干条纹的对比度为59%,而非相干时对比度为6%。中心条纹的宽度与理论计算结果吻合得很好。对同相模式而言,位相锁定激光器阵列输出达到113W,对应的斜率效率为38.5%。

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简述了光纤激光器的发展历史,重点介绍了双包层光纤激光器的进展并给出了高功率双包层光纤激光器的最新研究结果。评述了目前国内外高亮度激光的关键技术:光纤激光器的相干组束。介绍了几种典型的相干组束技术并分析了其工作原理。最后给出了相干组束研究的最新结果。

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探讨了3种不同自成像腔,即Talbot腔、自傅里叶变换腔(SF)和傅里叶变换自成像腔实现相干组束的机理和技术难点。介绍了利用光纤激光器,采用傅里叶变换自成像方法,实现1维2路和2维4路激光相干组束的实验情况,功率分别达到122W以及26W。

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以短的高掺杂浓度的掺铥硅基光纤为增益介质,采用790 nm波长的激光二极管(LD)为抽运源,得到了波长为2 μm的高功率激光输出。当光纤长度为7 cm时,激光器的阈值泵浦功率为135 mW,最大输出功率为1.09 W,斜率效率为9.6%(相对于耦合进光纤的抽运功率)。该激光器的输出稳定性在5%以内。此外,我们还观察分析了工作温度和其他腔结构参量对该激光器工作性能的影响。

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利用光纤-波导耦合器技术侧面泵浦一根4厘米长的短光纤,我们研制得到了一个红外波长的光纤激光器。该激光器的增益介质是横截面为矩形的掺钕磷酸盐玻璃光纤,其纤芯横截面尺寸为1.5×0.5 毫米,数值孔径为0.2。单横模激光可以通过该矩形光纤的增益-导引效应来获得。最大的激光输出功率为1.05瓦,斜率效率为10%。

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abstract {Rare earth ions doped multi-component glass fibers have important application in broad band fiber amplifier and up-conversion fiber lasers. In this paper, the mechanism and the progress of study on rare earth ions doped multi-component glass fibers in broad band fiber amplifier and up-conversion fiber lasers are introduced and reviewed. The questions and the applications of rare earth ions doped multi-component glass fibers in the future are also prospected. Based on the present research progress, it is suggested to further study the tellurite and bismuth glasses, which are used as fiber materials in broad band fiber amplifier. To up-conversion fiber laser, it is still need to further investigate novel glasses, which has low phonon energy and good physical and chemical properties.}

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亚碲酸盐玻璃由于具有较低的声子能量,加上其优良的化学稳定性、热稳定性和机械强度及其光学性能,其可作为光纤放大器和上转换光纤激光器的较理想的基质材料。文章介绍了上转换激光器的主要原理,并回顾了亚碲酸盐玻璃上转换激光器的研究进展。

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We present the results of a study that uses theoretical and experimental methods to investigate the characteristics of the upconversion luminescence of Tm3+/Yb3+ codoped TeO2-BiCl3 glass system as a function of the BiCl3 fraction. These glasses are potentially important in the design of upconversion fiber lasers. Effect of local environment around Tm3+ on upconversion fluorescence intensity was analyzed by theoretical calculations. The structure and spectroscopic properties were investigated in the experiments by measuring the Raman spectra, IR transmission spectra, and absorption and fluorescence intensities at room temperature. The results indicate that blue luminescence quantum efficiency increases with increasing BiCl3 content from 10 to 60 mol%, which were interpreted by the increase of asymmetry of glass structure, decrease of phonon energy and removing of OH- groups. (c) 2005 Elsevier B.V. All rights reserved.

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The upconversion properties of Er3+/Yb3+ codoped tellurite glasses and glass fibers with D-shape cladding under 980 mu excitation were investigated. Intense emission bands centered at 531, 546 and 658 nm corresponding to the transitions Er3+: H-2(11/2) -> I-4(15/2) , S-4(3/2) -> I-4(15/2) and F-4(9/2) -> I-4(15/2), respectively, were observed at room temperature. Compared with that in Er3+/Yb3+ codoped tellurite bulk glass, the upconversion luminescence becomes more efficient in the fiber geometry. The dependence of upconversion intensities on fiber geometry and possible upconversion mechanism are discussed and evaluated. The presented Er3+/Yb3+ codoped tellurite fibers with intense upconversion luminescence can be used as potential host materials for upconversion fiber lasers. (c) 2005 Elsevier B.V. All rights reserved.

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Over the past decades mode-locked fibre lasers have been extensively refined and developed, with most research efforts focussing on employing rare-earth doped fibres as the active elements [1]. This presents the problem that operation is limited to regions of the spectrum where such elements exhibit gain [1]. Raman amplification in silica fibre is an attractive way to overcome this spectral limitation, with gain available across the entire transparency window (300 nm - 2300 nm) [2-4]. There have been a number of reports utilising Raman gain in ultrashort pulse sources [2-4], however none using a broadband saturable absorber, such as carbon nanotubes [5-7] and graphene [7-9]. A broadband saturable absorber is an essential pre-requisite in order to fully exploit the wavelength flexibility provided by the Raman gain in short pulse mode-locked fiber lasers. © 2011 IEEE.

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Laser ablation of solid Silicon targets using pulsed Yb fiber lasers of pulse duration 1.5-400 ns Yb fiber lasers is studied in this work. Material responses of a range of pulse envelopes are examined including front peak (FP) and double peak (DP) pulses. Theoretical models for the interactions are examined and qualitative explanations of material response experiments are presented.

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Optically pumped ultrafast vertical external cavity surface emitting lasers (VECSELs), also referred to as semiconductor disk lasers (SDLs), are very attractive sources for ps- and fs-pulses in the near infrared [1]. So far VECSELs have been passively modelocked with semiconductor saturable absorber mirrors (SESAMs, [2]). Graphene has emerged as a promising saturable absorber (SA) for a variety of applications [3-5], since it offers an almost unlimited bandwidth and a fast recovery time [3-5]. A number of different laser types and gain materials have been modelocked with graphene SAs [3-4], including fiber [5] and solid-state bulk lasers [6-7]. Ultrafast VECSELs are based on a high-Q cavity, which requires very low-loss SAs compared to other lasers (e.g., fiber lasers). Here we develop a single-layer graphene saturable absorber mirror (GSAM) and use it to passively modelock a VECSEL. © 2013 IEEE.

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Two beta-diketones 4,4,4-trifluoro-1-2-thenoyl-1,3-butanedione (Htta) and 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione (Htfnb), which contain trifluoroalkyl chain, were selected as the main sensitizer for synthesizing Tm(L)(3)phen (L = tta, tfnb) complexes. The two near-infrared (NIR) luminescent thulium complexes have been covalently bonded to the ordered mesoporous material MCM-41 via a functionalized 1,10-phenanthroline (phen) group 5-(N,N-bis-3-(triethoxysilyl)propyl)ureyl-1,10-phenanthroline (phen-Si) [The resultant mesoporous materials are denoted as Tm(L)(3)phen-MCM-41 (L = tta, tfnb)]. The Tm(L)(3)phen-MCM-41 (L = tta, tfnb) mesoporous materials were characterized by small-angle Xray diffraction (XRD) and N-2 adsorption/desorption, and they show characteristic mesoporous structure of MCM-41.