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We report a mode-locked Alexandrite single pulse laser with cavity dumping. Mode locking was achieved by using an AOM and an EOM was used for Q-switching and cavity dumping. The instability of the single pulse laser energy output was reduced down to a tenth of that of the conventional single trigger system by introducing a novel double trigger system. The single pulse laser energy and pulse width were 100 mJ and 475 ps in multiple mode and 12.5 mJ and 275 ps in single mode, obtained without a laser amplifier.

We report the first investigation results of the nonlinear optical properties of As 2 Te 3 . More specifically, the nonlinear optical absorption properties of the prepared α-As 2 Te 3 were investigated at wavelengths of 1.56 and 1.9 μm using the open-aperture (OA) Z-scan technique. Using the OA Z-scan technique, the nonlinear absorption coefficients (β) of α-As 2 Te 3 were estimated in a range from (- 54.8 ± 3.4) × 10 4  cm/GW to (- 4.9 ± 0.4) × 10 4  cm/GW depending on the irradiance of the input beam at 1.56 μm, whereas the values did from (- 19.8 ± 0.8) × 10 4  cm/GW to (- 3.2 ± 0.1) × 10 4  cm/GW at 1.9 μm. In particular, the β value at 1.56 μm is an order of magnitude larger than the previously reported values of other group-15 sesquichalcogenides such as Bi 2 Se 3, Bi 2 Te 3, and Bi 2 TeSe 2 . Furthermore, this is the first time report on β value of a group-15 sesquichalcogenide at a 1.9-μm wavelength. The density functional theory (DFT) calculations of the electronic band structures of α-As 2 Te 3 were also conducted to obtain a better understanding of their energy band structure. The DFT calculations indicated that α-As 2 Te 3 possess sufficient optical absorption in a wide wavelength region, including 1.5 μm, 1.9 μm, and beyond (up to 3.7 μm). Using both the measured nonlinear absorption coefficients and the theoretically obtained refractive indices from the DFT calculations, the imaginary parts of the third-order optical susceptibilities (Im χ (3) ) of As 2 Te 3 were estimated and they were found to vary from (- 39 ± 2.4) × 10 -19 m 2 /V 2 to (- 3.5 ± 0.3) × 10 -19 m 2 /V 2 at 1.56 μm and (- 16.5 ± 0.7) × 10 -19 m 2 /V 2 to (- 2.7 ± 0.1) × 10 -19 m 2 /V 2 at 1.9 μm, respectively, depending on the irradiance of the input beam. Finally, the feasibility of using α-As 2 Te 3 for SAs was investigated, and the prepared SAs were thus tested by incorporating them into an erbium (Er)-doped fiber cavity and a thulium-holmium (Tm-Ho) co-doped fiber cavity for both 1.5 and 1.9 μm operation.

Photosensitive materials contain biologically engineered elements and are constructed using delicate techniques, with special attention devoted to efficiency, stability, and biocompatibility. However, to date, no photosensitive material has been developed to replace damaged visual-systems to detect light and transmit the signal to a neuron in the human body. In the current study, artificial nanovesicle-based photosensitive materials are observed to possess the characteristics of photoreceptors similar to the human eye. The materials exhibit considerably effective spectral characteristics according to each pigment. Four photoreceptors originating from the human eye with color-distinguishability are produced in human embryonic kidney (HEK)-293 cells and partially purified in the form of nanovesicles. Under various wavelengths of visible light, electrochemical measurements are performed to analyze the physiological behavior and kinetics of the photoreceptors, with graphene, performing as an electrode, playing an important role in the lipid bilayer deposition and oxygen reduction processes. Four nanovesicles with different photoreceptors, namely, rhodopsin (Rho), short-, medium-, and longwave sensitive opsin 1 (1SW, 1MW, 1LW), show remarkable color-dependent characteristics, consistent with those of natural human retina. With four different light-emitting diodes for functional verification, the photoreceptors embedded in nanovesicles show remarkably specific color sensitivity. This study demonstrates the potential applications of light-activated platforms in biological optoelectronic industries., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

2D transition metal carbides, nitrides, and carbonitrides called MXenes have attracted increasing attention due to their outstanding properties in many fields. By performing systematic density functional theory calculations, here we show that MXenes can serve as excellent terahertz detecting materials. Giant optical absorption and extinction coefficients are observed in the terahertz range in the most popular MXene, namely, Ti 3 C 2 , which is regardless of the stacking degree. Various other optical properties have been investigated as well in the terahertz range for in-depth understanding of its optical response. We find that the thermoelectric figure of merit (ZT) of stacked Ti 3 C 2 flakes is comparable to that of carbon nanotube films. Based on excellent terahertz absorption and decent thermoelectric efficiency in MXenes, we finally suggest the promise of MXenes in terahertz detection applications, which includes terahertz bolometers and photothermoelectric detectors. Possible ZT improvements are discussed in large-scale MXene flake films and/or MXene-polymer composite films.

We report a new efficient light guidance along a liquid core using an open V-groove. Guiding properties were analyzed using finite element method in terms of the single mode guidance condition, and the corresponding modal birefringence. We experimentally demonstrated a silica V-groove fiber with an opening angle of 40°, which was spliced to single mode fibers at both ends. A liquid with the refractive index of 1.455 was filled to serve as a core along a maximum length of 47cm. We confirmed the single mode guidance and birefringence consistent to theory, which will enable polarimetric liquid sensing.

2D transition metal carbides, nitrides, and carbonitides called MXenes have attracted much attention due to their outstanding properties. However, MXene's potential in laser technology is not explored. It is demonstrated here that Ti 3 CN, one of MXene compounds, can serve as an excellent mode-locker that can produce femtosecond laser pulses from fiber cavities. Stable laser pulses with a duration as short as 660 fs are readily obtained at a repetition rate of 15.4 MHz and a wavelength of 1557 nm. Density functional theory calculations show that Ti 3 CN is metallic, in contrast to other 2D saturable absorber materials reported so far to be operative for mode-locking. 2D structural and electronic characteristics are well conserved in their stacked form, possibly due to the unique interlayer coupling formed by MXene surface termination groups. Noticeably, the calculations suggest a promise of MXenes in broadband saturable absorber applications due to metallic characteristics, which agrees well with the experiments of passively Q-switched lasers using Ti 3 CN at wavelengths of 1558 and 1875 nm. This study provides a valuable strategy and intuition for the development of nanomaterial-based saturable absorbers opening new avenues toward advanced photonic devices based on MXenes., (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Surface plasmon polaritons have attracted broad attention in the optoelectronics field due to their ability to merge nanoscale electronics with high-speed optical communication. As the complexity of optoelectronic devices increases to meet various needs, this integration has been hampered by the low coupling efficiency of light to plasmonic modes. Here we present a method to maximize the coupling of far-field optical waves to plasmonic waves for arbitrarily complex devices. The method consists of experimentally identifying the eigenchannels of a given nanostructure and shaping the wavefront of incident light to a particular eigenchannel that maximizes the generation of plasmonic waves. Our proposed approach increases the coupling efficiency almost four-fold with respect to the uncontrolled input. Our study will help to facilitate the integration of electronics and photonics.

We present terahertz (THz) transmission control by several uniquely designed patterns of nano-slot antenna array. Collinearly aligned slot antenna arrays have been usually applied to THz filters with frequency band tunability by their geometry. Normally the amplitude in transmission (reflection) in the collinear alignment case can be varied via rotating the azimuthal angle with a sinusoidal trend, which can limit their utilization and performance only at fixed angle between the alignment of the resonant antennas and incident beam polarization. To pursue a variety of metamaterial uses, here, we present polarization-independent THz filters using variously aligned antenna array (asterisk, chlorophyll, and honeycomb patterns) in such counter-intuitive aspects. Besides, unprecedented multi resonance behaviors were observed in chlorophyll and honeycomb patterns, which can be explained with interferences by adjacent structures. The measured spectra were analyzed by harmonic oscillator model with simplified coupling between slots and their adjacent.

Merging multiple microprocessors with high-speed optical networks has been considered a promising strategy for the improvement of overall computation power. However, the loss of the optical communication bandwidth is inevitable when interfacing between optical and electronic components. Here we present an on-chip plasmonic switching device consisting of a two-dimensional (2D) disordered array of nanoholes on a thin metal film that can provide multiple-input and multiple-output channels for transferring information from a photonic to an electronic platform. In this device, the surface plasmon polaritons (SPPs) generated at individual nanoholes become uncorrelated on their way to the detection channel due to random multiple scattering. We exploit this decorrelation effect to use individual nanoholes as independent antennas, and demonstrated that more than 40 far-field incident channels can be delivered simultaneously to the SPP channels, an order of magnitude improvement over conventional 2D patterned devices.

We experimentally demonstrate the use of a bulk-like, MoSe 2 -based saturable absorber (SA) as a passive harmonic mode-locker for the production of femtosecond pulses from a fiber laser at a repetition rate of 3.27 GHz. By incorporating a bulk-like, MoSe 2 /PVA-composite-deposited side-polished fiber as an SA within an erbium-doped-fiber-ring cavity, mode-locked pulses with a temporal width of 737 fs to 798 fs can be readily obtained at various harmonic frequencies. The fundamental resonance frequency and the maximum harmonic-resonance frequency are 15.38 MHz and 3.27 GHz (212th harmonic), respectively. The temporal and spectral characteristics of the output pulses are systematically investigated as a function of the pump power. The output pulses exhibited Gaussian-temporal shapes irrespective of the harmonic order, and even when their spectra possessed hyperbolic-secant shapes. The saturable absorption and harmonic-mode-locking performance of our prepared SA are compared with those of previously demonstrated SAs that are based on other transition metal dichalcogenides (TMDs). To the best of the authors' knowledge, the repetition rate of 3.27 GHz is the highest frequency that has ever been demonstrated regarding the production of femtosecond pulses from a fiber laser that is based on SA-induced passive harmonic mode-locking.

Monolayer MoS2 (1L-MoS2) has photoluminescence (PL) properties that can greatly vary via transition between neutral and charged exciton PLs depending on carrier density. Here, for the first time, we present a chemical doping method for reversible transition between neutral and charged excitons of 1L-MoS2 using chlorine-hydrogen-based plasma functionalization. The PL of 1L-MoS2 is drastically increased by p-type chlorine plasma doping in which its intensity is easily tuned by controlling the plasma treatment duration. We find that despite their strong adhesion, a post hydrogen plasma treatment can very effectively dedope chlorine adatoms in a controllable way while maintaining robust structural integrity, which enables well-defined reversible PL control of 1L-MoS2. After exhaustive chlorine dedoping, the hydrogen plasma process induces n-type doping of 1L-MoS2, degrading the PL further, which can also be recovered by subsequent chlorine plasma treatment, extending the range of tunable PL into a bidirectional regime. This cyclically-tunable carrier doping method can be usefully employed in fabricating highly-tunable n- and p-type domains in monolayer transition-metal dichalcogenides suitable for two-dimensional electro-optic modulators, on-chip lasers, and spin- and valley-polarized light-emitting diodes.

Recently, evidence was presented that certain single-walled carbon nanotubes (SWNTs) possess helical defective traces, exhibiting distinct cleaved lines, yet their mechanical characterization remains a challenge. On the basis of the spiral growth model of SWNTs, here we present atomic details of helical defects and investigate how the tensile behaviors of SWNTs change with their presence using molecular dynamics simulations. SWNTs have exhibited substantially lower tensile strength and strain than theoretical results obtained from a seamless tubular structure, whose physical origin cannot be explained either by any known SWNT defects so far. We find that this long-lasting puzzle could be explained by assuming helical defects in SWNTs, exhibiting excellent agreement with experimental observation. The mechanism of this tensile process is elucidated by analyzing atomic stress distribution and evolution, and the effects of the chirality and diameter of SWNTs on this phenomenon are examined based on linear elastic fracture mechanics. This work contributes significantly to our understanding of the growth mechanism, defect hierarchies, and mechanical properties of SWNTs.

Tungsten ditelluride (WTe2) is a layered material that exhibits excellent magnetoresistance and thermoelectric behaviors, which are deeply related with its distorted orthorhombic phase that may critically affect the lattice dynamics of this material. Here, we report comprehensive characterization of Raman spectra of WTe2 from bulk to monolayer using experimental and computational methods. We find that mono and bi-layer WTe2 are easily identified by Raman spectroscopy since two or one Raman modes that are observed in higher-layer WTe2 are greatly suppressed below the noise level in the mono- and bi-layer WTe2, respectively. In addition, the frequency of in-plane A1(7) mode of WTe2 remains almost constant as the layer number decreases, while all the other Raman modes consistently blueshift, which is completely different from the vibrational behavior of hexagonal metal dichalcogenides. First-principles calculation validates experimental results and reveals that anomalous lattice vibrations in WTe2 are attributed to the formation of tungsten chains that make WTe2 structurally one-dimensional.

The modification of deoxyribonucleic acid (DNA) samples by sequencing the order of bases and doping copper ions opens the possibility for the design of novel nanomaterials exhibiting large optical nonlinearity. We investigated the nonlinear characteristics of copper-ion doped double crossover DNA samples for the first time to the best of our knowledge by using Z-scan and four-wave mixing methods. To accelerate the nonlinear characteristics, we prepared two types of unique DNA nanostructures composed of 148 base pairs doped with copper ions with a facile annealing method. The outstanding third-order nonlinear optical susceptibility of the copper-ion-doped DNA solution, 1.19 × 10(-12) esu, was estimated by the conventional Z-scan measurement, whereas the four-wave mixing experiment was also investigated. In the visible spectral range, the copper-ion-doped DNA solution samples provided competent four-wave mixing signals with a remarkable conversion efficiency of -4.15 dB for the converted signal at 627 nm. The interactions between DNA and copper ions contribute to the enhancement of nonlinearity due to structural and functional changes. The present study signifies that the copper-ion-doped double crossover DNA is a potential candidate as a highly efficient novel material for further nonlinear optical applications.

We demonstrate the use of an all-fiberized, mode-locked 1.94 μm laser with a saturable absorption device based on a tungsten disulfide (WS2)-deposited side-polished fiber. The WS2 particles were prepared via liquid phase exfoliation (LPE) without centrifugation. A series of measurements including Raman spectroscopy, scanning electron microscopy (SEM), and atomic force microscopy (AFM) revealed that the prepared particles had thick nanostructures of more than 5 layers. The prepared saturable absorption device used the evanescent field interaction mechanism between the oscillating beam and WS2 particles and its modulation depth was measured to be ~10.9% at a wavelength of 1925 nm. Incorporating the WS2-based saturable absorption device into a thulium-holmium co-doped fiber ring cavity, stable mode-locked pulses with a temporal width of ~1.3 ps at a repetition rate of 34.8 MHz were readily obtained at a wavelength of 1941 nm. The results of this experiment confirm that WS2 can be used as an effective broadband saturable absorption material that is suitable to passively generate pulses at 2 μm wavelengths.

We experimentally demonstrate femtosecond harmonic mode-locking of a fiber laser using a bulk-structured Bi(2)Te(3) topological insulator (TI)-deposited on a side-polished fiber as a mode-locker. A bulk-structured Bi(2)Te(3) TI film was prepared at a thickness of ~20 μm using a mechanical exfoliation method. Using the mode-locker in an erbium-doped fiber ring cavity, it was experimentally shown that harmonically mode-locked pulses with temporal widths of 630 ~700 fs could readily be generated upto the 55th harmonics. The pulse repetition rate was shown to be tunable from the fundamental resonance frequency of 14.07 MHz to the harmonic frequency of 773.85 MHz with increasing pump power. The pumping efficiency was measured at ~3.36 MHz/mW. The side mode suppression ratio (SMSR) was observed to be more than 27.3 dB over all harmonic orders, while the corresponding signal-to-noise ratio (SNR) ranged from 46.3 to 63 dB.

Control of near-field waves is the key to going beyond the diffraction limit in imaging and manipulating target objects. Here we present the focusing of plasmonic waves, a type of near-field waves, by the wavefront shaping of far-field waves. We coupled far-field waves to a random array of holes on a thin gold film to generate speckled plasmonic waves. By controlling the phase pattern of the incident waves with the wavelength of 637 nm, we demonstrated the focusing of plasmonic waves down to 170 nm at arbitrary positions. Our study shows the possibility of using disordered nanoholes as a plasmonic lens with high flexibility in the far-field control.

We experimentally demonstrate the use of a bulk-structured Bi(2)Te(3) topological insulator (TI) as an ultrafast mode-locker to generate femtosecond pulses from an all-fiberized cavity. Using a saturable absorber based on a mechanically exfoliated layer about 15 μm thick deposited onto a side-polished fiber, we show that stable soliton pulses with a temporal width of ~600 fs can readily be produced at 1547 nm from an erbium fiber ring cavity. Unlike previous TI-based mode-locked laser demonstrations, in which high-quality nanosheet-based TIs were used for saturable absorption, we chose to use a bulk-structured Bi(2)Te(3) layer because it is easy to fabricate. We found that the bulk-structured Bi(2)Te(3) layer can readily provide sufficient nonlinear saturable absorption for femtosecond mode-locking even if its modulation depth of ~15.7% is much lower than previously demonstrated nanosheet-structured TI-based saturable absorbers. This experimental demonstration indicates that high-crystalline-quality atomic-layered films of TI, which demand complicated and expensive material processing facilities, are not essential for ultrafast laser mode-locking applications.

An in-depth experimental investigation was conducted into the use of a graphene oxide-based saturable absorber implemented on a side-polished fiber platform for femtosecond pulse generation in the 2 μm region. First, it was experimentally shown that an all-fiberized thulium-holmium (Tm-Ho)-codoped fiber ring laser with reduced cavity length can produce stable femtosecond pulses by incorporating a graphene oxide-deposited side-polished fiber. Second, the measurement accuracy issue in obtaining a precise pulse-width value by use of an autocorrelator together with a silica fiber-based 2 μm-band amplifier was investigated. It showed that the higher-order soliton compression effect caused by the combination of anomalous dispersion and Kerr nonlinearity can provide incorrect pulse-width information. Third, an experimental investigation into the precise role of the graphene oxide-deposited side-polished fiber was carried out to determine whether its polarization-dependent loss (PDL) can be a substantial contributor to mode-locking through nonlinear polarization rotation. By comparing its performance with that of a gold-deposited side-polished fiber, the PDL contribution to mode-locking was found to be insignificant, and the dominant mode-locking mechanism was shown to be saturable absorption due to mutual interaction between the evanescent field of the oscillated beam and the deposited graphene oxide particles.

We have constructed a wireless monitoring test platform with a sub-nA resolution signal amplification/processing circuit (SAPC) and a wireless communication network to test the real-time remote monitoring of the signals from carbon nanotube (CNT) sensors. The operation characteristics of the CNT sensors can also be measured by the ISD-VSD curve with the SAPC. The SAPC signals are transmitted to a personal computer by Bluetooth communication and the signals from the computer are transmitted to smart phones by Wi-Fi communication, in such a way that the signals from the sensors can be remotely monitored through a web browser. Successful remote monitoring of signals from a CNT sensor was achieved with the wireless monitoring test platform for detection of 0.15% methanol vapor with 0.5 nA resolution and 7 Hz sampling rate.

We present the results of an investigation regarding a Q-switched mode-locked fiber laser scheme based on a cavity modulation frequency detuning technique. The approach is based on undamped laser relaxation oscillations occurring due to frequency detuning in the fundamental cavity resonance frequency. Through a range of experiments with an erbium-doped, fiber-based, ring-cavity laser, this approach has been shown to be capable of generating high-quality Q-switched mode-locked pulses from an optical fiber-based laser. The maximum frequency detuning range for a stable Q-switched mode-locking operation has been observed to vary depending on the pump power used. We found that the highest pulse peak power was obtained at the frequency detuning threshold at which the operation changed from the mode-locking to the Q-switched mode-locking regime.

Here we examine the waveguide dispersion property of slot waveguides, approaching/analyzing the given problem with respect to the normalized index contrast, Δnslot-core/ncore and Δncore-clad/ncore between adjacent layers . For two index contrasts of concern, it is found that their contributions to slot waveguide dispersions are substantially different, with Δnslot-core and Δncore-clad each acting preferentially on short- and long-wavelength regions. Additional degrees of freedom in the waveguide design, such as the effect of absolute refractive index and waveguide geometry are also investigated to enable flexible tuning of the waveguide dispersion. Focusing on the unexplored regime of slot waveguides design in short wavelength (<1 μm), we also study the feasibility of low-threshold super-continuum sources using a Ta2O5/TiO2/silica slot, either of two-octave spectral width (0.467–1.581 μm), or of one-octave, near unity coherence |g12(1)| = 1.

We fabricated carbon nanotube (CNT) based chemical sensors for marine applications by photolithography process, where the electrodes were insulated by photoresist exposing only the carbon nanotube sensing section (2 microm gap width) for detection of ammonium ions (NH4+) in 35 per thousand NaCI solution used as artificial seawater environment. The I-V curve of the CNT sensor was measured by sweeping the source-drain voltage from -3 to 3 V and the on/off ratio of the CNT sensor was measured to be 20 when the gate voltage was swept from -5 to 5 V and from these results the CNTs were found to appear as a p-type semiconductor. All of the cocktail solutions prepared for experiment were measured to have -pH 6 which implied 99.9% of NH4+ remained ionized. We successfully detected 10, 100, 1000 nM (0.18, 1.8, 18 ppb) concentration of NH4+ in 35 per thousand NaCI solutions by using the CNT sensor.

Presented herein is the use of an ultrafast Si-based variable optical attenuator (VOA) as a Q-switch for rare earth-doped fiber lasers. The ultrafast VOA is based on a forward-biased p-i-n diode integrated with a ridge waveguide, which was originally designed and optimized for WDM channel power equalization in optical communication systems. By incorporating a Si-based VOA with a transient time of ~410 ns into an erbium-doped fiber-based Fabry-Perot cavity it has been shown that stable Q-switched pulses possessing a temporal width of less than ~86 ns can be readily obtained at a repetition rate of up to ~1 MHz. The laser's peak power of ~38 W is shown to be obtainable at 20 kHz with a slope efficiency of ~21%.

Recently, integrated flexible devices based on silicon nanowires (Si-NWs) have received significant attention as high performance flexible devices. However, most previous assembly methods can generate only specifically-shaped devices and require unconventional facilities, which has been a major hurdle for industrial applications. Herein, we report a simple but very efficient method for assembling Si-NWs into virtually generally-shape patterns on flexible substrates using only conventional microfabrication facilities, allowing us to mass-produce highly flexible low-noise devices. As proof of this method, we demonstrated the fabrication of highly bendable top-gate transistors based on Si-NWs. These devices showed typical n-type semiconductor behaviors, and exhibited a much lower noise level compared to previous flexible devices based on organic conductors or other nanowires. In addition, the gating behaviors and low-noise characteristics of our devices were maintained, even under highly bent conditions.

Nanoscale sensors based on single-walled carbon nanotube (SWNT) networks have been considered impractical due to several fundamental limitations such as a poor sensitivity and small signal-to-noise ratio. Herein, we present a strategy to overcome these fundamental problems and build highly-sensitive low-noise nanoscale sensors simply by controlling the structure of the SWNT networks. In this strategy, we prepared nanoscale width channels based on aligned SWNT networks using a directed assembly strategy. Significantly, the aligned network-based sensors with narrower channels exhibited even better signal-to-noise ratio than those with wider channels, which is opposite to conventional random network-based sensors. As a proof of concept, we demonstrated 100 nm scale low-noise sensors to detect mercury ions with the detection limit of approximately 1 pM, which is superior to any state-of-the-art portable detection system and is below the allowable limit of mercury ions in drinking water set by most government environmental protection agencies. This is the first demonstration of 100 nm scale low-noise sensors based on SWNT networks. Considering the increased interests in high-density sensor arrays for healthcare and environmental protection, our strategy should have a significant impact on various industrial applications.

A semiconductor optical amplifier-based all-optical read-only memory (ROM) is successfully demonstrated through simulations using a one-level simplification method optimized for optical logic circuits. Design details are presented, and advantages are discussed in comparison with an all-optical ROM-employing decoder. We demonstrate that eight characters can be stored at each address in the American Standard Code for Information Interchange.

We have developed a method to selectively assemble and align carbon nanotubes (CNTs) on soft substrates for use as flexible biosensors. In this strategy, a thin oxide layer was deposited on soft substrates via low temperature plasma enhanced chemical vapor deposition, and a linker-free assembly process was applied on the oxide surface where the assembly of carbon nanotubes was guided by methyl-terminated molecular patterns on the oxide surface. The electrical characterization of the fabricated CNT devices exhibited a typical p-type gating effect and 1/f noise behavior. The bare oxide regions near CNTs were functionalized with glutamate oxidase to fabricate selective biosensors to detect two forms of glutamate substances existing in different situations: L-glutamic acid, a neurotransmitting material, and monosodium glutamate, a food additive.

By using the gain nonlinearity characteristics of semiconductor optical amplifier, an all-optical binary half adder at 10 Gbps is demonstrated. The half adder operates in a single mechanism, which is cross gain modulation. The half adder utilizes two logic functions of SUM and CARRY, which can be demonstrated by using XOR and AND gates, respectively. The extinction ratios of both XOR and AND gates are about 6.1 dB. By achieving this experiment, we also explored the possibilities for the enhanced complex logic operation and higher chances for multiple logic integration.

For the first time to our knowledge, pulse-amplitude equalization of rational-harmonically mode-locked fiber ring laser pulses has been experimentally demonstrated using a polarization-maintaining laser resonator without any additional device. The pulse-amplitude distribution of the laser pulses was controlled by the modulator driving power, and stable pulse-amplitude-equalized pulses with repetition rates of 20, 30, and 40 GHz have been obtained in the linear region of the modulator.

We propose and demonstrate a photonic phase shifter based a on vector-sum technique that uses polarization-maintaining fibers (PMFs). We achieved a continuous and full phase shift up to 2pi at 30.48 GHz by controlling the polarization state of the light injected into two pieces of PMF of different lengths and applying two different modulator bias voltages.

We have found theoretically that the intracavity dispersion of a laser is independent of the pumping power and wavelength and that the resonant group-velocity dispersion vanishes. We have experimentally observed that the intracavity dispersion of an erbium-doped fiber laser was independent of the pumping power and wavelength within the measuring error, which agrees well with our theoretical predictions.