Low-noise mode-locking in a GHz repetition rate Tm3+-doped fiber laser.

We demonstrate a GHz repetition rate mode-locked Tm3+-doped fiber laser with low noise. Based on a home-made Tm3+-doped barium gallo-germanate fiber with reduced dispersion, a broad optical spectrum of mode-locking is achieved, and its amplified spontaneous emission quantum-limited timing jitter is largely suppressed. Besides, we carefully investigate the influence of the intracavity pump strength on the noise performance of the mode-locked pulses and find that manipulating the intracavity pump power can be an effective method for optimizing the timing jitter and relative intensity noise (RIN). Particularly, RIN, which originated from the relaxation oscillation, can be effectively suppressed by 33 dB at offset frequencies of >1 MHz. The integrated timing jitter and RIN are only 7.9 fs (10 kHz-10 MHz) and 0.05% (10 Hz-10 MHz), respectively.

Enhanced 2-µm and upconversion luminescence properties regulated by network structure in Ho3+/Yb3+ co-doped germanate laser glasses.

Rare-earth (RE) ions doped laser glass has attracted the interest of many researchers because of its numerous potential applications in planar waveguides and fiber lasers. In this work, the 2-µm and upconversion luminescence properties of Ho3+ are simultaneously enhanced through the design of components used to regulate the network structure of the germanate glass. Furthermore, the thermal, structural, and spectroscopic properties of the Ho3+/Yb3+ co-doped germanate laser glass are systematically investigated. It is noted that the calculated gain coefficient of the Nb2O5 modified germanate laser glass can reach as high as 3.05 cm-1 at 2047 nm. These results suggest that the prepared germanate laser glass with superior performances is a promising candidate for 2-µm mid-infrared laser materials applications.

Broadband 1.0†µm emission in Nd3+/Yb3+ co-doped phosphate glasses and fibers for photonic applications.

In this work, the spectroscopic properties of 1.0 µm emission in Nd3+/Yb3+ co-doped phosphate glasses were systematically investigated under 808 nm excitation. Notably, broadband 1.0 µm emission with a full width at half maximum (FWHM) of 96 nm was obtained in the phosphate glass doped with 2 mol.% Nd2O3 and 1 mol.% Yb2O3. In addition, the energy transfer microscopic parameter and transfer efficiency were analyzed. What is more, multimaterial fibers with Nd3+/Yb3+ co-doped phosphate glass core and silicate cladding were successfully drawn by using the molten core method. An intense 1.0 µm amplified spontaneous emission (ASE) can be realized in a 3 cm long multimaterial fiber. More importantly, the FWHM of the ASE can reach as large as 60 nm when excited at 976 nm. These results demonstrate that the Nd3+/Yb3+ co-doped phosphate glasses and fibers are promising gain materials for amplifier and laser applications in photonics.

Broadband near-infrared amplified spontaneous emission of Er3+-doped germanate glass fiber.

Er3+-doped glass and fiber are very attractive for near-infrared (NIR) lasers and photonic applications. In this work, the full width at half maximum (FWHM) of NIR fluorescence emission of the Er3+-doped germanate glass can be broadened from 72 to 99 nm when Al2O3 was added. In addition, the spectroscopic properties, including absorption and emission spectra, Judd-Ofelt intensity parameters, absorption and emission cross sections, gain coefficient, and fluorescence lifetime, of the Al2O3-modified germanate glass were systematically investigated. What is more, silicate-clad heavily Er3+-doped germanate core multimaterial fibers were successfully drawn by a rod-in-tube method. Notably, broadband NIR amplified spontaneous emission (ASE) with an FWHM of 120 nm was achieved in this new fiber. To the best of our knowledge, this is the largest FWHM reported for Er3+-doped germanate glass fibers. These results suggest that the as-drawn Er3+-doped germanate glass fiber with superior performances is a promising candidate for broadband optical amplification.

Femtosecond laser nanostructuring on a 4H-SiC surface by tailoring the induced self-assembled nanogratings.

Ultrafast laser micromachining of crystalline silicon carbide (SiC) has great perspectives in aerospace industry and integrated circuit technique. In this report, we present a study of femtosecond laser nanostructuring on the surface of an n-type 4H-SiC single crystal. Except for uniform nanogratings, new types of large-area periodic structures including nanoparticle array and nanoparticle-nanograting hybrid structures were induced on the surface of 4H-SiC by scanning irradiation. The effects of pulse energy, scan speed, and the polarization direction on the morphology and periodicity of nanogratings were systematically explored. The proper parameter window for nanograting formation in pulse energy-scan speed landscape is depicted. Both the uniformity and the periodicity of the induced nanogratings are polarization dependent. A planar light attenuator for linear polarized light was demonstrated by aligning the nanogratings. The transition between different large-area periodic structures is achieved by simultaneous control of pulse energy and scan interval using a cross scan strategy. These results are expected to open up an avenue to create and manipulate periodic nanostructures on SiC crystals for photonic applications.

Broadband high-gain Tm3+/Ho3+ co-doped germanate glass multimaterial fiber for fiber lasers above 2 µm.

High-gain Tm3+/Ho3+ co-doped optical fibers are urgently desired for high-repetition-rate mode-locked fiber lasers at >2 µm. Here, Tm3+/Ho3+ co-doped germanate glass with low hydroxyl (OH-) content was prepared by the conventional melt-quenching method combined with the reaction atmosphere procedure (RAP) dehydration technique. The doping concentrations of Tm2O3 and Ho2O3 are 2.5 mol.% (7.1 wt.%) and 0.25 mol.% (0.7 wt.%), respectively. Thanks to the high Tm3+ doping (7.1 wt.%) and low energy transfer efficiency (19.8%) between Tm3+ and Ho3+ ions, it enables achieving broadband and high-gain performance in the 2 µm region. Then a silicate-clad Tm3+/Ho3+ co-doped germanate core multimaterial fiber was successfully drawn by using the rod-in-tube method, which has a broadband amplified spontaneous emission (ASE) with a full width at half-maximum (FWHM) of 247.8 nm at 2 µm. What is more, this new fiber has a high gain per unit length of 4.52 dB/cm at 1.95 µm. Finally, an all-fiber-integrated passively mode-locked fiber laser was built by using this broadband high-gain fiber. The mode-locked pulses operate at 2068.05 nm, and the fundamental repetition rate is up to 4.329 GHz. To the best of our knowledge, this is the highest fundamental repetition rate for the all-fiber passively mode-locked fiber laser above 2 µm. These results suggest that the as-drawn multimaterial fibers with broadband high-gain characteristics are promising for high-repetition-rate ultrafast fiber lasers.

4.3†GHz fundamental repetition rate passively mode-locked fiber laser using a silicate-clad heavily Tm3+-doped germanate core multimaterial fiber.

We report a silicate-clad heavily Tm3+-doped germanate core multimaterial fiber that is successfully drawn by using a rod-in-tube method. This new fiber has a high gain per unit length of 6.11 dB/cm at 1.95 µm, which is, to the best of the authors' knowledge, the highest gain per unit length reported so far for Tm3+-doped glass fibers. By virtue of this high-gain glass fiber, an all-fiber-integrated passively mode-locked fiber laser with a fundamental repetition rate up to 4.3 GHz is demonstrated. Remarkably, the generated pulse operating at 1968 nm exhibits a signal-to-noise ratio of >76 dB in the radio-frequency domain. These results suggest that the silicate-clad heavily Tm3+-doped germanate core multimaterial fiber can act as a key building block for high repetition rate mode-locked fiber lasers at 2 µm.

Controllable structural tailoring for enhanced ∼2 µm emission in heavily Tm3+-doped germanate glasses.

Heavily Tm3+-doped glass fibers are urgently desired for ∼2µm single-frequency fiber lasers and high-repetition-rate mode-locked fiber lasers. Here the structure of glass networks was tuned through controlling the numbers of non-bridging oxygens and bridging oxygens by adjusting the composition of the glasses, hence increasing the Tm3+ doping concentration of germanate glasses. The increased flexibility of the glass networks favors the distribution of Tm3+ ions to decrease fluorescence quenching, which was confirmed by the experimental and theoretical results. A heavily Tm3+ (9.8×1020ions/cm3)-doped germanate glass was successfully fabricated without quenching by tuning the components of the glass. To the best of our knowledge, the Tm3+ ion doping concentration is the highest reported level in Tm3+-doped glasses and fibers. The results suggest that the heavily Tm3+-doped germanate glass is highly promising for fabricating ∼2µm glass fibers with high gain per unit length.

Silicate-clad heavily Yb3+ doped phosphate core multimaterial fiber with a high gain per unit length for mode-locked fiber laser applications.

Silicate-clad heavily Yb3+ doped phosphate core multimaterial fiber (MF) was successfully drawn by using a molten core method, which has a high gain per unit length of 5.44 dB/cm at 1.06 µm. What is more, an all-fiber-integrated passively mode-locked fiber laser based on a 5 cm long MF was built. The mode-locked pulses operate at 1055 nm with a period of ∼555ps, and the fundamental repetition rate is 1.787 GHz. For the first time, to the best of our knowledge, we demonstrate the realization of a mode-locked fiber laser with a gigahertz fundamental repetition rate based on a silicate-clad heavily Yb3+ doped phosphate core MF.

Tm:YAG ceramic derived multimaterial fiber with high gain per unit length for 2 µm laser applications.

In this work, Tm:YAG (Tm:${{\rm Y}_3}{{\rm Al}_5}{{\rm O}_{12}}$Y3Al5O12) ceramic-derived multimaterial fiber was fabricated by using the molten core method, which has a high gain per unit length of 2.7 dB/cm at 1950 nm. To our knowledge, this is the highest gain per unit length at 2 µm band in similar Tm:YAG-derived multimaterial fibers. A distributed Bragg reflector (DBR) fiber laser was built based on a 10-cm-long as-drawn fiber. The achieved 1950 nm laser, which has a maximum output power of $\sim{240}\;{\rm mW}$∼240mW and a slope efficiency of 16.5%, was pumped by a self-developed 1610 nm fiber laser. What is more, an all-fiber-integrated passively mode-locked fiber laser based on the 10-cm-long as-drawn fiber was realized. The mode-locked pulses operate at 1950 nm with duration of $\sim{380}\;{\rm ps}$∼380ps, and the repetition rate is 26.45 MHz. The results described here indicate that the Tm:YAG ceramic-derived multimaterial fiber with high gain per unit length has promising applications in 2 µm all-fiber fiber lasers.

Broadband 2 µm amplified spontaneous emission of Ho/Cr/Tm:YAG crystal derived all-glass fibers for mode-locked fiber laser applications.

Broadband ∼2 µm amplified spontaneous emissions with a full width at half-maximum (FWHM) varying from ∼206 to ∼234 nm were obtained from the Ho/Cr/Tm:yttrium aluminum garnet (YAG) crystal derived fibers, which were drawn using a molten core method. The core-cladding structure of the as-drawn fibers was preserved completely, and the core was found to be amorphous. What is more, an all-fiber-integrated passively mode-locked laser based on an 8 cm long Ho/Cr/Tm:YAG crystal derived all-glass fiber was built which, to the best of our knowledge, is the first demonstration of a mode-locked fiber laser in a similar YAG derived fiber. The mode-locked pulses operate at 1.95 µm with duration of ∼118 ps, and the repetition rate is ∼9.5 MHz. Limited by the bandwidth of the fiber grating used in the laser cavity, the mode-locking spectrum has a relatively narrow FWHM of ∼0.09 nm. These results suggest that the broadband YAG crystal derived all-glass fibers are promising for ultrafast fiber lasers applications.

High-efficiency sub-watt in-band-pumped single-frequency DBR Tm3+-doped germanate fiber laser at 1950 nm.

Based on a 1.8-cm-long heavily Tm3+-doped germanate fiber and being in-band-pumped by a 1610 nm single-mode laser, a high-efficiency and high-power single-frequency distribute Bragg reflector (DBR) fiber laser emitting at 1950 nm is demonstrated. The DBR fiber laser has a maximum output power of ~617 mW and a slope efficiency for the absorbed pump power reaches to more than 42.2%. A stable single-longitudinal-mode laser output with a signal-to-noise ratio of greater than 63 dB is realized. The measured relative intensity-noise of the fiber laser reaches to around -150 dB/Hz at frequencies of over 8.4 MHz. It is beneficial to exploit the sub-watt and high-efficiency single-frequency laser from fiber oscillators directly, especially in the application of multiple paths coherent beam combination and optical medical technology.

Gamma radiation induced darkening in barium gallo-germanate glass.

Barium gallo-germanate (BGG) glass is an important glass matrix material used for mid-infrared transmission and mid-infrared fiber laser. In this study, we investigated the γ-ray irradiation induced darkening effect of BGG glass. Optical transmittance spectra, electron paramagnetic resonance (EPR) and thermoluminescence (TL) spectra were employed to investigate the γ-ray irradiation induced defects. Two kinds of Ge-related defects in the irradiated BGG glass, named Ge-related non-bridging oxygen hole center (Ge-NBOHC) and Ge-related electron centers (GEC), were verified. In addition, the absorption bands of the two defects have been separated and the peak absorptivity of Ge-NBOHC and GEC defects is at 375 nm and 315 nm, respectively.

Tm³âº doped barium gallo-germanate glass single-mode fibers for 2.0 µm laser.

Tm³âº doped barium gallo-germanate (BGG) glass has emerged as a promising 2.0 µm laser material offering excellent optical property. Unfortunately, low anti-crystallization ability and high OH⁻ content of the glass have hindered the fabrication of high-quality optical fibers. In this paper, La2O3 and Y2O3 were added into BGG glass to enhance the glass anti-crystallization ability. Additionally, the optimized Reaction Atmosphere Procedure (RAP) was utilized to minimize OH⁻ content. Continuous Tm³âº doped BGG glass single-mode (SM) fibers were successfully obtained by the rod-in-tube technique for the first time to our best knowledge. A 140 mW all-fiber laser at 1.95 µm was demonstrated using a 9.7-cm-long as-drawn Tm³âº doped BGG glass SM fiber upon excitation of a home-made 1568 nm fiber laser.

Reactive molten core fabrication of glass-clad Se(0.8)Te(0.2) semiconductor core optical fibers.

Phosphate glass-clad optical fibers comprising amorphous Se(0.8)Te(0.2) semiconductor core were fabricated by a reactive molten core approach. The Se(0.8)Te(0.2) crystals were precipitated in core region by a postdrawing annealing process, which were confirmed by X-ray diffraction, micro-Raman spectra, electron probe X-ray micro-analyzer, and transmission electron microscope measurement results. A two-cm-long crystalline Se(0.8)Te(0.2) semiconductor core optical fiber, electrically contacted to external circuitry through the fiber end facets, exhibits a two-orders-of-magnitude change in conductivity between dark and illuminated states. The great discrepancy in light and dark conductivity suggests that such crystalline Se(0.8)Te(0.2) semiconductor core optical fibers have promising applications in optical switch and photoconductivity of optical fiber array.

Recent Advances in Self-Powered Tactile Sensing for Wearable Electronics.

With the arrival of the Internet of Things era, the demand for tactile sensors continues to grow. However, traditional sensors mostly require an external power supply to meet real-time monitoring, which brings many drawbacks such as short service life, environmental pollution, and difficulty in replacement, which greatly limits their practical applications. Therefore, the development of a passive self-power supply of tactile sensors has become a research hotspot in academia and the industry. In this review, the development of self-powered tactile sensors in the past several years is introduced and discussed. First, the sensing principle of self-powered tactile sensors is introduced. After that, the main performance parameters of the tactile sensors are briefly discussed. Finally, the potential application prospects of the tactile sensors are discussed in detail.

High-Performance n-Type Bi2Te3 Thermoelectric Fibers with Oriented Crystal Nanosheets.

High-performance thermoelectric fibers with n-type bismuth telluride (Bi2Te3) core were prepared by thermal drawing. The nanosheet microstructures of the Bi2Te3 core were tailored by the whole annealing and Bridgman annealing processes, respectively. The influence of the annealing processes on the microstructure and thermoelectric performance was investigated. As a result of the enhanced crystalline orientation of Bi2Te3 core caused by the above two kinds of annealing processes, both the electrical conductivity and thermal conductivity could be improved. Hence, the thermoelectric performance was enhanced, that is, the optimized dimensionless figure of merit (ZT) after the Bridgman annealing processes increased from 0.48 to about 1 at room temperature.

Enhanced N-Type Bismuth-Telluride-Based Thermoelectric Fibers via Thermal Drawing and Bridgman Annealing.

N-type bismuth telluride (Bi2Te3) based thermoelectric (TE) fibers were fabricated by thermal drawing and Bridgman annealing, and the influence of Bridgman annealing on the TE properties of n-type Bi2Te3-based TE fibers was studied. The Bridgman annealing enhanced the electrical conductivity and Seebeck coefficient because of increasing crystalline orientation and decreasing detrimental elemental enrichment. The TE performance of n-type Bi2Te3-based TE fibers was improved significantly by enhancing the power factor. Hence the power factor increased from 0.14 to 0.93 mW/mK2, and the figure-of-merit value is from 0.11 to 0.43 at ~300 K, respectively.

Enhanced Thermoelectric Properties of Bi2 Te3 -Based Micro-Nano Fibers via Thermal Drawing and Interfacial Engineering.

High-performance thermoelectric (TE) materials with great flexibility and stability are urgently needed to efficiently convert heat energy into electrical power. Recently, intrinsically crystalline, mechanically stable, and flexible inorganic TE fibers that show TE properties comparable to their bulk counterparts have been of interest to researchers. Despite remarkable progress in moving TE fibers toward room-temperature TE conversion, the figure-of-merit value (ZT) and bending stability still need enhancement. Herein, interfacial-engineering-enhanced TE properties of micro-nano polycrystalline TE fibers fabricated by thermally drawing Bi2 Te3 -based bulks in a glass-fiber template are reported. The interfacial engineering effect comes from generating stress-induced oriented nanocrystals to increase electrical conductivity and producing strain-distorted interfaces to decrease thermal conductivity. The 4 µm-diameter fibers achieve a 40% higher ZT (≈1.4 at 300 K) than their bulk counterparts and show a reversible bending radius of 50 µm, approaching the theoretical elastic limit. This fabrication strategy works for a wide range of inorganic TE materials and benefits the development of fiber-based micro-TE devices.

Multiphase Transition toward Colorless Bismuth-Germanate Scintillating Glass and Fiber for Radiation Detection.

The applications of scintillating fiber in high-resolution medical imaging, remote radiation monitoring, and microbeam radiation therapy have raised a growing demand of bismuth-germanate (BGO) glass fiber. However, the task of construction of colorless BGO glass fiber has been met with limited success. Here, we present a renewable process that can help to achieve BGO scintillating fiber, based on glass relaxation and crystallization mediated dissolution of unexpected Bi center. The experimental results indicate that the strategy can improve the optical transmittance up to more than 73.17% at 483 nm, which is ∼6.28 times higher than that of the conventional material. Importantly, the obtained nanostructured BGO exhibits bright visible luminescence under excitation with X-ray. Furthermore, it can host various types of rare-earth dopants, and the radiation-induced luminescence can be tuned in a wide waveband region from visible to infrared waveband. In addition, colorless BGO fiber with bright emission is also successfully constructed, and the radiation probing test demonstrates the achievement of ∼19.48 times improvement in the detection sensitivity. Our results highlight the approach based on the dynamic glass relaxation may provide new opportunities for construction of scintillating glass fiber and compact radiation fiber detector.