Improved Hydrogen Capping Effect in n-Type Crystalline Silicon Solar Cells by SiN(Si-Rich)/SiN(N-Rich) Stacked Passivation

The effect of hydrogen capping of SiN(Si-rich)/SiN(N-rich) stacks for n-type c-Si solar cells was investigated. Use of a passivation layer consisting of Si-rich SiN with a refractive index (n) of 2.7 and N-rich SiN with a refractive index of 2.1 improved the thermal stability. A single SiN passivation layer with a refractive index of 2.05 resulted in an initial lifetime of 200 μs whereas the layer with a refractive index of 2.7 resulted in a high initial lifetime of 2 ms, but the layer degraded rapidly after firing. A stacked passivation layer with refractive indices of 2.1 and 2.7 had a stable lifetime of 1.5 ms with an implied open-circuit voltage (iV _oc) of 720 mV after firing. The thermally stable passivation mechanism with changing amounts of Si–N and Si–H bonding was analyzed by Fourier-transform infrared (FTIR) spectroscopy. Incorporation of the SiN _x stack layer (2.7 + 2.1) into the passivated rear of n-type Cz silicon screen-printed solar cells resulted in energy conversion efficiency of 19.69%. Improved internal quantum efficiency in the long-wavelength range above 900 nm, with V _oc of 630 mV, is mainly because of superior passivation of the rear surface compared with conventional solar cells.     

Functionality of Dual‐Phase Lithium Storage in a Porous Carbon Host for Lithium‐Metal Anode

Lithium (Li) metal is regarded as the most attractive anode material for high‐energy Li batteries, but it faces unavoidable challenges—uncontrollable dendritic growth of Li and severe volume changes during Li plating and stripping. Herein, a porous carbon framework (PCF) derived from a metal–organic framework (MOF) is proposed as a dual‐phase Li storage material that enables efficient and reversible Li storage via lithiation and metallization processes. Li is electrochemically stored in the PCF upon charging to 0 V versus Li/Li⁺ (lithiation), making the PCF surface more lithiophilic, and then the formation of metallic Li phase can be induced spontaneously in the internal nanopores during further charging below 0 V versus Li/Li⁺ (metallization). Based on thermodynamic calculations and experimental studies, it is shown that atomically dispersed zinc plays an important role in facilitating Li plating and that the reversibility of Li storage is significantly improved by controlled nanostructural engineering of 3D porous nanoarchitectures to promote the uniform formation of Li. Moreover, the MOF‐derived PCF does not suffer from macroscopic volume changes during cycling. This work demonstrates that the nanostructural engineering of porous carbon structures combined with lithiophilic element coordination would be an effective approach for realizing high‐capacity, reversible Li‐metal anodes.     

Joint utility function-based scheduling for two-way communication services in wireless networks

A type of joint utility function-based scheduling is proposed for two-way communication services in wireless networks. The scheduling of uplink and downlink services is done jointly so that the base station selects a user efficiently and fairly while considering the channel state of both the uplink and the downlink. Because a user generally has two communication links, an uplink and a downlink, the overall satisfaction with a communication service can be formulated as the sum of the quality of the uplink and downlink services. However, most of the previous types of scheduling for the uplink and downlink were designed separately and independently. This paper proposes a joint scheduling algorithm for integrated uplink and downlink services: a base station selects a user while simultaneously considering both the uplink channel state and the downlink channel state. An analytical model is developed for the purpose of determining the scheduling metric, the system throughput, and the level of fairness. The numerical and computer simulation results show that in comparison with conventional proportional fair scheduling the proposed joint scheduling achieves a better throughput while satisfying the fairness among users.     

High‐Performance Transition Metal Dichalcogenide Photodetectors Enhanced by Self‐Assembled Monolayer Doping

Most doping research into transition metal dichalcogenides (TMDs) has been mainly focused on the improvement of electronic device performance. Here, the effect of self‐assembled monolayer (SAM)‐based doping on the performance of WSe₂‐ and MoS₂‐based transistors and photodetectors is investigated. The achieved doping concentrations are ≈1.4 × 10¹¹ for octadecyltrichlorosilane (OTS) p‐doping and ≈10¹¹ for aminopropyltriethoxysilane (APTES) n‐doping (nondegenerate). Using this SAM doping technique, the field‐effect mobility is increased from 32.58 to 168.9 cm² V^?1 s in OTS/WSe₂ transistors and from 28.75 to 142.2 cm² V^?1 s in APTES/MoS₂ transistors. For the photodetectors, the responsivity is improved by a factor of ≈28.2 (from 517.2 to 1.45 × 10⁴ A W^?1) in the OTS/WSe₂ devices and by a factor of ≈26.4 (from 219 to 5.75 × 10³ A W^?1) in the APTES/MoS₂ devices. The enhanced photoresponsivity values are much higher than that of the previously reported TMD photodetectors. The detectivity enhancement is ≈26.6‐fold in the OTS/WSe₂ devices and ≈24.5‐fold in the APTES/MoS₂ devices and is caused by the increased photocurrent and maintained dark current after doping. The optoelectronic performance is also investigated with different optical powers and the air‐exposure times. This doping study performed on TMD devices will play a significant role for optimizing the performance of future TMD‐based electronic/optoelectronic applications.     

Molecular dynamics simulations and experimental studies of the thermomechanical response of an epoxy thermoset polymer

We report a detailed comparison between molecular dynamics predictions and experimental results for a wide range of thermo-mechanical properties of an epoxy resin system: diglycidyl ether of bisphenol A (DGEBA) cured with 3,3′ diamino-diphenyl sulfone (33DDS). A set of carefully designed and characterized experiments provides validation data for the simulations that predict the molecular structure and properties of the thermoset. Our results show that current state-of-the-art molecular dynamics simulations provide quantitative predictions for this epoxy system in its glassy state, including elastic moduli, coefficient of thermal expansion and specific heat. The glass transition temperature is also accurately predicted once a correction is included to account for the difference in cooling rates between the simulations and experiments. Our results also indicate that viscoelastic and thermal properties of the thermoset polymer in its rubbery state are more challenging to predict since the effect of timescales is not well understood.     

Synthesis of boron nitride nanotubes using thermal chemical vapor deposition of ball milled boron powder

Thermal chemical vapor deposition (TCVD) produces relatively pure boron nitride nanotubes (BNNTs), while it may not be enough for production. A ball milling–annealing process is beneficial in quantity; however, the generation of the impurity is most concerned. In this regard, we explored the dual syntheses of BNNTs based on the chemical reactions of solid and gaseous boron with nitrogen, respectively. Synthesis mechanisms for both were also analyzed by presenting the stepwise reaction routes. With these understandings, the production of BNNTs could be increased, while the impurities are reduced when compared with the individual one, once the experimental conditions are optimized.     

A low-loss single-pole six-throw switch based on compact RF MEMS switches

A low-loss single-pole six-throw (SP6T) switch using very compact metal-contact RF microelectromechanical system (MEMS) series switches is presented. The metal-contact MEMS switch has an extremely compact active area of 0.4 mm /spl times/ 0.3 mm, thus permitting the formation of an SP6T MEMS switch into the RF switch with a total area of 1 mm/sup 2/. The MEMS switch shows an effective spring constant of 746 N/m and an actuation time of 8.0 /spl mu/s. It has an isolation loss from -64.4 to -30.6dB and an insertion loss of 0.08-0.19 dB at 0.5-20 GHz. Furthermore, in order to evaluate RF performances of the SP6T MEMS switch, as well as those of the single-pole single-throw RF MEMS series switch, we have performed small-signal modeling based on a parameter-extraction method. Accurate agreement between the measured and modeled RF performances demonstrates the validity of the small-signal model. The SP6T switch performed well with an isolation loss from -62.4 to -39.1dB and an insertion loss of 0.19-0.70 dB from dc to 6 GHz between the input port and each output port.     

2-D WO3 decorated with Pd for rapid gasochromic and electrical hydrogen sensing

The ultrathin two-dimensional (2D) nanomaterials display unique properties owing to their ultrahigh specific surface area and strong quantum confinement of electrons in two dimensions. In this work, we fabricated a rapid gasochromic and electrical hydrogen sensing system containing 2D WO₃ and Pd nanoparticles. 2D WO₃ nano-plates (NP) are synthesized using sol–gel method and Pd nanoparticles are coated on WO₃ by green photochemical deposition method. The sensor is fabricated by dispersing the 2D WO₃/Pd composite on filter paper. In presence of hydrogen gas, 2D WO₃/Pd composite produces visible change in color from brown to dark blue. With the fabricated sensor, as low as 0.1% H₂ gas in air at room temperature can be easily detected using electrical sensing scheme whereas for higher concentration from 1 to 100%, eye readable gasochromic scheme can be utilized. The use of 2D WO₃ decreased the response time in great deal compared to WO₃ nanoparticles indicating the advantage of 2D structure in fabricating rapid response H₂ sensors. The proposed method is simple and can be easily employed to large scale fabrication system for commercial applications.