Parallel optical transmitter module using angled fibers and a V-grooved silicon optical bench for VCSEL array

We propose an advanced structure of optical subassembly (OSA) for packaging of the vertical-cavity surface-emitting laser (VCSEL) array, using (111) facet mirror of the V-groove ends formed in a silicon optical bench (SiOB) and angled fiber apertures. The feature of our OSA can provide a low optical crosstalk between neighboring channels, a low feedback reflection, and a large misalignment tolerance along the V-groove. We describe the optimized design of fiber angle, VCSEL position, and fiber position. The fabricated OSA structure consists of 12 channels of angled fiber array, 54.7/spl deg/ V-grooves, Au-coated mirrors on (111) end facet of the V-grooves, and flip-chip-bonded VCSEL array on a SiOB. In this structure, the beam emitted from the VCSEL is deflected at the 54.7/spl deg/ mirror of (111) end facet and propagated into the angled fiber. The angled fiber array was polished by 57/spl deg/. Fabricated OSAs showed a coupling efficiency of 30%-50% that is 25 times larger than that obtained from an OSA with a vertically flat fiber array. Our OSA showed large misalignment tolerance of about 90 /spl mu/m along the longitudinal direction in the V-groove. We fabricated a parallel optical transmitter module using the OSA and demonstrated 12 channels /spl times/2.5 Gb/s data transmission with a clear eye diagram.     

Broad-band erbium-doped fiber amplifier with double-passconfiguration

We demonstrate a broad-band silica-based erbium-doped fiber amplifier (EDFA) with double-pass configuration. The signal gain and noise figure are obtained more than 24 dB and less than 6 dB, respectively, for 1526-1562 nm and 1569-1605 nm. The same signal gain can be achieved with 53% less pump power and 45% shorter erbium-doped fiber length, compared to a conventional parallel type EDFA. Furthermore, the noise figure and power conversion efficiency are improved for the wavelength range     

Blind adaptive multiuser detection for DS/SSMA communications withgeneralized random spreading

A new spreading scheme and an accompanying blind adaptive receiver structure are proposed for direct-sequence spread-spectrum multiple-access communications in a slowly-varying, frequency-selective fading channel. Each user's spreading sequence is given by the Kronecker product of a long-period pseudonoise (PN) sequence, which is accurately modeled by a random sequence, and a short-length deterministic signature code. This spreading scheme bridges the gap between pure PN spreading and pure short-code spreading schemes. It is shown that with this spreading scheme, the channel response to the desired signal component is easily estimated without relying on the spectral decomposition of the signal correlation matrix. With the estimate of the channel response, the receiver suppresses interference based on the maximum signal-to-interference ratio criterion. The blind adaptive receiver requires only coarse timing information and a priori knowledge of the desired user's PN sequence for adaptation. Numerical results show that the adaptive receiver significantly suppresses interference by successfully estimating the channel response and the interference statistics with a low computational complexity. An extension to spatio-temporal processing using an array antenna is also discussed     

压电驱动膜片式微型气泵

提出一种结构新颖的压电驱动膜片式微型气泵，对其输出流量、膜片的振幅等参数进行了理论分析，在此基础上设计、制作了微型气泵样机，并进行了测试实验。这种气泵在结构上充分利用了双压电梁端部位移大的优点，并利用两根双压电梁将膜片悬起，增加了容积变化率和输出流量，并具有结构简单，功耗低，厚度小，无电磁噪音，可靠性高等优点，在微型电子器件的冷却、微型燃料电池换气等方面显示出良好的应用前景。根据实验，微型气泵的一阶固有频率约为120Hz，在谐振状态下，当驱动电压为50V时，其输出流量为192mL／min，功耗小于23mW。     

Non-functionalized soluble diketopyrrolopyrrole: Simplest p-channel core for organic field-effect transistors

We report the synthesis, characterization and behavior in field-effect transistors of non-functionalized soluble diketopyrrolopyrrole (DPP) core with only a solubilizing alkyl chain (i.e. –C₁₆H₃₃ or –C₁₈H₃₇) as the simplest p-channel semiconductor. The characteristics were evaluated by UV–vis and fluorescence spectroscopy, X-ray diffraction, cyclic voltammetry (CV), thermal analysis, atomic force microscopy (AFM) and density functional theory (DFT) calculation. For top-contact field-effect transistors, two types of active layers were prepared either by a solution process (as a 1D-microwire) or thermal vacuum deposition (as a thin-film) on a cross-linked poly(4-vinylphenol) gate dielectric. All the devices showed typical p-channel behavior with dominant hole transports. The device made with 1D-microwiress of DPP-R18 showed field-effect mobility in the saturation region of 1.42 × 10^?2 cm²/V s with I_ON/I_OFF of 1.82 × 10³. These findings suggest that the non-functionalized soluble DPP core itself without any further functionalization could also be used as a p-channel semiconductor for low-cost organic electronic devices.     

Automatic Transformation of Membrane‐Type Electronic Devices into Complex 3D Structures via Extrusion Shear Printing and Thermal Relaxation of Acrylonitrile–Butadiene–Styrene Frameworks

This work demonstrates a means of automatic transformation from planar electronic devices to desirable 3D forms. The method uses a spatially designed thermoplastic framework created via extrusion shear printing of acrylonitrile–butadiene–styrene (ABS) on a stress‐free ABS film, which can be laminated to a membrane‐type electronic device layer. Thermal annealing above the glass transition temperature allows stress relaxation in the printed polymer chains, resulting in an overall shape transformation of the framework. In addition, the significant reduction in the Young's modulus and the ability of the polymer chains to reflow in the rubbery state release the stress concentration in the electronic device layer, which can be positioned outside the neutral mechanical plane. Electrical analyses and mechanical simulations of a membrane‐type Au electrode and indium gallium zinc oxide transistor arrays before and after transformation confirm the versatility of this method for developing 3D electronic devices based on planar forms.     

Gallium-nitride microwave Doherty power amplifier with 40 W PEP and 68% PAE

A 40 W gallium-nitride microwave Doherty power amplifier for WCDMA repeater applications is presented. The main amplifier and peaking amplifier are implemented using two 20 W PEP GaN HEMTs. Performance is evaluated for broadband gain, power efficiency and adjacent-channel-power-ratio (ACPR). Experimental results of the GaN Doherty amplifier yielded a power gain of over 11 dB from 1.8 to 2.5 GHz, 68% power added efficiency at 40 W peak power. Good linearity performance of -48 dBc ACPR is obtained at a peak-to-average ratio of 9.8 dB.     

Disclosing the Role of Defect-Engineered Metal–Organic Frameworks in Mixed Matrix Membranes for Efficient CO2 Separation: A Joint Experimental-Computational Exploration

Incorporation of defects in metal–organic frameworks (MOFs) offers new opportunities for manipulating their microporosity and functionalities. The so-called “defect engineering” has great potential to tailor the mass transport properties in MOF/polymer mixed matrix membranes (MMMs) for challenging separation applications, for example, CO₂ capture. This study first investigates the impact of MOF defects on the membrane properties of the resultant MOF/polymer MMMs for CO₂ separation. Highly porous defect-engineered UiO-66 nanoparticles are successfully synthesized and incorporated into a CO₂-philic crosslinked poly(ethylene glycol) diacrylate (PEGDA) matrix. A thorough joint experimental/simulation characterization reveals that defect-engineered UiO-66/PEGDA MMMs exhibit nearly identical filler–matrix interfacial properties regardless of the defect concentrations of their parental UiO-66 filler. In addition, non-equilibrium molecular dynamics simulations in tandem with gas transport studies disclose that the defects in MOFs provide the MMMs with ultrafast transport pathways mainly governed by diffusivity selectivity. Ultimately, MMMs containing the most defective UiO-66 show the most enhanced CO₂/N₂ separation performance—CO₂ permeability = 470 Barrer (four times higher than pure PEGDA) and maintains CO₂/N₂ selectivity = 41—which overcomes the trade-off limitation in pure polymers. The results emphasize that defect engineering in MOFs would mark a new milestone for the future development of optimized MMMs.     

Non‐Volatile Polymer Electroluminescence Programmable with Ferroelectric Field‐Induced Charge Injection Gate

Electroluminescence (EL) of organic and polymeric fluorescent materials programmable in the luminance is extremely useful as a non‐volatile EL memory with the great potential in the variety of emerging information storage applications for imaging and motion sensors. In this work, a novel non‐volatile EL memory in which arbitrarily chosen EL states are programmed and erased repetitively with long EL retention is demonstrated. The memory is based on utilizing the built‐in electric field arising from the remnant polarization of a ferroelectric polymer which in turn controls the carrier injection of an EL device. A device with vertically stacked components of a transparent bottom electrode/a ferroelectric polymer/a hole injection layer/a light emitting layer/a top electrode successfully emits light upon alternating current (AC) operation. Interestingly, the device exhibits two distinctive non‐volatile EL intensities at constant reading AC voltage, depending upon the programmed direct current (DC) voltage on the ferroelectric layer. DC programmed and AC read EL memories are also realized with different EL colors of red, green and blue. Furthermore, more than four distinguishable EL states are precisely addressed upon the programmed voltage input each of which shows excellent EL retention and multiple cycle endurance of more than 10⁵ s and 10² cycles, respectively.     

Use of Mesoscopic Host Matrix to Induce Ferrimagnetism in Antiferromagnetic Spinel Oxide

Despite the advances in the methods for fabricating nanoscale materials, critical issues remain, such as the difficulties encountered in anchoring, and the deterioration in their stability after integration with other components. These issues need to be addressed to further increase the scope of their applicability. In this study, using epitaxial mesoscopic host matrices, materials are spatially confined at the nanoscale, and are supported, anchored, and stabilized. They also exhibit properties distinct from the bulk counterparts proving their high quality nanoscale nature. ZnFe₂O₄ and SrTiO₃ are used as the model confined material and host matrix, respectively. The ZnFe₂O₄ phases are spatially confined by the SrTiO₃ mesoscopic matrix and have strongly enhanced ferrimagnetic properties as compared to bulk and plain thin films of ZnFe₂O₄, with a Curie temperature of ≈500 K. The results of a series of control experiments and characterization measurements indicate that cationic inversion, which originates from the high interface‐to‐volume ratio of the ZnFe₂O₄ phase in the ZnFe₂O₄–SrTiO₃ nanocomposite film, is responsible for the magnetization enhancement. An exchange bias is observed, owing to the coexistence of ferrimagnetic and antiferromagnetic regions in the confined ZnFe₂O₄ phase. The magnetic properties are dependent on the ZnFe₂O₄ crystallite size, which can be controlled by the growth conditions.