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Proceedings ArticleDOI

Fiber-integrated second harmonic generation modules for visible and near-visible picosecond pulse generation

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TLDR
In this paper, the authors report on the development of fiber-coupled frequency doubling modules and their application to novel fiberintegrated picosecond pulse sources in the visible and near-visible.
Abstract
Second harmonic generation (SHG) is a ubiquitous technique for extending the spectral coverage of laser sources into regions that would otherwise be technologically challenging to access. SHG schemes typically rely on the use of bulk optical components, resulting in systems with large footprints requiring precise optical alignment. Integration of the SHG components into a single unit facilitates the implementation of compact, robust and turn-key sources, suitable for applications in biophotonic imaging, amongst others. We report on the development of fiber-coupled frequency doubling modules and their application to novel fiberintegrated picosecond pulse sources in the visible and near-visible. The modules employ a simple, single-pass configuration using a periodically-poled lithium niobate (PPLN) crystal as the nonlinear conversion medium. They are readily adaptable for different fiber pump laser configurations and are configurable with either fiber-coupled or collimated free-space outputs. Two sources using the modules are presented, operating at 780 nm and 560 nm. The 780 nm source utilizes an erbium master oscillator power fiber amplifier (MOPFA) scheme. SHG was performed in a 35 mm long crystal, generating 3.5 W of 780 nm radiation with a pulse duration of 410 ps at 50 MHz and conversion efficiencies exceeding 20%. Results of this source being used for parametric wavelength conversion in photonic crystal fiber are discussed. The 560 nm source was based on SHG of a Raman amplified CW diode pumped by a pulsed ytterbium-fiber MOPFA. This source generated 450 mW of average power with conversion efficiencies greater than 20%.

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Proceedings ArticleDOI

High power laser source for atom cooling based on reliable telecoms technology with all fibre frequency stabilisation

T. Legg, +1 more
- 22 Feb 2017 - 
TL;DR: In this paper, a laser system suitable for Rb atom cooling, based on a 1560nm DFB laser and erbium doped fiber amplifier, is described, where the laser output is frequency doubled with fiber coupled periodically poled LiNbO3 to a wavelength of 780nm.
References
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Journal ArticleDOI

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: A new type of scanning fluorescence microscope capable of resolving 35 nm in the far field is proposed, overcome the diffraction resolution limit by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point-spread function.
Journal Article

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: In this paper, the authors proposed a new type of scanning fluorescence microscope capable of resolving 35 nm in the far field by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point spread function.

Nonlinear optics

TL;DR: In this method, non-linear susceptibility tensors are introduced which relate the induced dipole moment to a power series expansion in field strengths and the various experimental observations are described and interpreted in terms of this formalism.
Journal ArticleDOI

STED microscopy reveals crystal colour centres with nanometric resolution.

TL;DR: Based on a far-field fluorescence-based optical super-resolution scheme, this article resolved densely packed individual fluorescent color centres inside crystals with a farfield spatial resolution of 5.8 nm without photobleaching.
Journal ArticleDOI

Nanoscale resolution in GFP-based microscopy.

TL;DR: The attainment of subdiffraction resolution using stimulated emission depletion (STED) microscopy with GFP-labeled samples is reported, marking the advent of nanoscale biological microscopeopy with genetically encoded markers.
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