Systematic Design of High‐Resolution High‐Frequency Cascade Continuous‐Time Sigma‐Delta Modulators

This paper introduces a systematic top‐down and bottom‐up design methodology to assist the designer in the implementation of continuous‐time (CT) cascade sigma‐delta (ΣΔ) modulators. The salient features of this methodology are (a) flexible behavioral modeling for optimum accuracy‐efficiency trade‐offs at different stages of the top‐down synthesis process, (b) direct synthesis in the continuous‐time domain for minimum circuit complexity and sensitivity, (c) mixed knowledge‐based and optimization‐based architectural exploration and specification transmission for enhanced circuit performance, and (d) use of Pareto‐optimal fronts of building blocks to reduce re‐design iterations. The applicability of this methodology will be illustrated via the design of a 12‐bit 20 MHz CT ΣΔ modulator in a 1.2 V 130 nm CMOS technology.     

Design of High‐Performance Disordered Half‐Heusler Thermoelectric Materials Using 18‐Electron Rule

Ternary half‐Heusler (HH) alloys display intriguing functionalities ranging from thermoelectric to magnetic and topological properties. For thermoelectric applications, stable HH alloys with a nominal valence electron count (VEC) of 18 per formula or defective HH alloys with a VEC of 17 or 19 are assumed to be promising candidates. Inspired by the pioneering efforts to design a TiFe_0.5Ni_0.5Sb double HH alloy by combining 17‐electron TiFeSb and 19‐electron TiNiSb HH alloys, both high‐performance n‐type and p‐type materials based on the same parent TiFe_0.5Ni_0.5Sb are developed. First‐principles calculation results demonstrate their beneficial band structure having a high band degeneracy that contributes to their large effective mass and thereby maintains their high Seebeck coefficient values. Due to the strong Fe/Ni disorder effect, TiFe_0.5Ni_0.5Sb exhibits a much lower lattice thermal conductivity than does TiCoSb, consistent with very recently reported results. Furthermore, tuning the ratio of Fe and Ni leads to achieving both p‐ and n‐types, and alloying Ti by Hf further enhances the thermoelectric performance significantly. A peak ZT of ≈1 and ≈0.7 at 973 K are achieved in the p‐type and n‐type based on the same parent, respectively, which are beneficial and promising for real applications.     

Point Defect Engineering of High‐Performance Bismuth‐Telluride‐Based Thermoelectric Materials

Developing high‐performance thermoelectric materials is one of the crucial aspects for direct thermal‐to‐electric energy conversion. Herein, atomic scale point defect engineering is introduced as a new strategy to simultaneously optimize the electrical properties and lattice thermal conductivity of thermoelectric materials, and (Bi,Sb)₂(Te,Se)₃ thermoelectric solid solutions are selected as a paradigm to demonstrate the applicability of this new approach. Intrinsic point defects play an important role in enhancing the thermoelectric properties. Antisite defects and donor‐like effects are engineered in this system by tuning the formation energy of point defects and hot deformation. As a result, a record value of the figure of merit ZT of ≈1.2 at 445 K is obtained for n‐type polycrystalline Bi₂Te_2.3Se_0.7 alloys, and a high ZT value of ≈1.3 at 380 K is achieved for p‐type polycrystalline Bi_0.3Sb_1.7Te₃ alloys, both values being higher than those of commercial zone‐melted ingots. These results demonstrate the promise of point defect engineering as a new strategy to optimize thermoelectric properties.     

Boronic Acid Decorated Defective Metal–Organic Framework Nanoreactors for High‐Efficiency Carbohydrates Separation and Labeling

Separation and labeling are the crucial steps for the carbohydrates identification and detection in the important field of biochemistry, biomedicine, glycomics, and glycobiology. Herein, for the first time, a boronic acid decorated defective metal–organic framework (B‐D‐MI‐100) nanoreactor is designed, which integrates fast separation and labeling of carbohydrates into one step. Without the sacrifice of internal room space, the incorporation of abundant functional boronic acid groups into the framework is achieved through metal–ligand–fragment coassembly strategy. And the novel solid phase orientation labeling approach performed within elaborate Cr based B‐D‐MIL‐100 nanoreactor is facile to avoid the conformation transition of carbohydrates occurred in classical liquid‐phase labeling. As a result, the novel approach presents several merits, including high separation efficiency (almost all of the incorporated boronic acid groups are available), much fast labeling reaction speed (labeling reaction time is decreased from 7 h to 3 min), high purity of the product, and three orders of magnitude lower applicable carbohydrate concentration for labeling. Thus, this new approach advances the idea to efficiently detect and identify trace carbohydrates in important fields such as glycomics and glycobiology.     

Design of Parasitic Inductance Reduction in GaN Cascode FET for High‐Efficiency Operation

This paper presents a method of parasitic inductance reduction for high‐speed switching and high‐efficiency operation of a cascode structure with a low‐voltage enhancement‐mode silicon (Si) metal–oxide–semiconductor field‐effect transistor (MOSFET) and a high‐voltage depletion‐mode gallium nitride (GaN) field‐effect transistor (FET). The method is proposed to add a bonding wire interconnected between the source electrode of the Si MOSFET and the gate electrode of the GaN FET in a conventional cascode structure package to reduce the most critical inductance, which provides the major switching loss for a high switching speed and high efficiency. From the measured results of the proposed and conventional GaN cascode FETs, the rising and falling times of the proposed GaN cascode FET were up to 3.4% and 8.0% faster than those of the conventional GaN cascode FET, respectively, under measurement conditions of 30 V and 5 A. During the rising and falling times, the energy losses of the proposed GaN cascode FET were up to 0.3% and 6.7% lower than those of the conventional GaN cascode FET, respectively.     

High‐Efficiency InP‐Based Photocathode for Hydrogen Production by Interface Energetics Design and Photon Management

The solar energy conversion efficiency of photoelectrochemical (PEC) devices is usually limited by poor interface energetics, limiting the onset potential, and light reflection losses. Here, a three‐pronged approach to obtain excellent performance of an InP‐based photoelectrode for water reduction is presented. First, a buried p–n⁺ junction is fabricated, which shifts the valence band edge favorably with respect to the hydrogen redox potential. Photoelectron spectroscopy substantiates that the shift of the surface photovoltage is mainly determined by the buried junction. Second, a periodic array of InP nanopillars is created at the surface of the photoelectrode to substantially reduce the optical reflection losses. This device displays an unprecedented photocathodic power‐saved efficiency of 15.8% for single junction water reduction. Third, a thin TiO₂ protection layer significantly increases the stability of the InP‐based photoelectrode. Careful design of the interface energetics based on surface photovoltage spectroscopy allows obtaining a PEC cell with stable record performance in water reduction.     

High‐Efficiency Near‐Infrared Fluorescent Organic Light‐Emitting Diodes with Small Efficiency Roll‐Off: A Combined Design from Emitters to Devices

The simultaneous realization of high quantum yield and exciton utilizing efficiency (η_r) is still a formidable challenge in near‐infrared (NIR) fluorescent organic light‐emitting diodes (FOLEDs). Here, to achieve a high quantum yield, a novel NIR dye, 4,9‐bis(4‐(diphenylamino)phenyl)‐naphtho[2,3‐c ][1,2,5]selenadiazole, is designed and synthesized with a large highest occupied molecular orbital/lowest unoccupied molecular orbital overlap and an aggregation‐induced emission property, which demonstrates a high photoluminescence quantum yield of 27% at 743 nm in toluene and 29% at 723 nm in a blend film. For a high η_r, an orange‐emitting thermally activated delayed fluorescent material, 1,2‐bis(9,9‐dimethyl‐9,10‐dihydroacridine)‐4,5‐dicyanobenzene, is chosen as the sensitizing host to harvest triplet excitons in devices. The optimized devices achieve a good η_r of 45.7% and a high external quantum efficiency up to 2.65% at 730 nm, with a very small efficiency roll‐off of 2.41% at 200 mA cm^?2, which are among the most efficient values for NIR‐FOLEDs over 700 nm. The effective utilization of triplet excitons via the thermally activated delayed fluorescence‐sensitizing host will pave a way to realize high‐efficiency NIR‐FOLEDs with small efficiency roll‐off.     

Temperature‐Mediated Engineering of Graphdiyne Framework Enabling High‐Performance Potassium Storage

Graphdiyne (GDY), an emerging type of carbon allotropes, possesses fascinating electrical, chemical, and mechanical properties to readily spark energy applications in the realm of Li‐ion and Na‐ion batteries. Nevertheless, rational design of GDY architectures targeting advanced K‐ion storage has rarely been reported to date. Herein, the first example of synthesizing GDY frameworks in a scalable fashion to realize superb potassium storage for high‐performance K‐ion battery (KIB) anodes is showcased. To begin with, first principles calculations provide theoretical guidances for analyzing the intrinsic potassium storage capability of GDY. Meanwhile, the specific capacity is predicted to be as high as 620 mAh g^?1, which is considerably augmented as compared with graphite (278 mAh g^?1). Experimental tests then reveal that prepared GDY framework indeed harvests excellent electrochemical performance as a KIB anode, achieving high specific capacity (≈505 mAh g^?1 at 50 mA g^?1), outstanding rate performance (150 mAh g^?1 at 5000 mA g^?1) and favorable cycling stability (a high capacity retention of over 90% after 2000 cycles at 1000 mA g^?1). Furthermore, kinetic analysis reveals that capacitive effect mainly accounts for the K‐ion storage, with operando Raman spectroscopy/ex situ X‐ray photoelectron spectroscopy identifying good electrochemical reversibility of GDY.     

A Discrete‐Amplitude Pulse Width Modulation for a High‐Efficiency Linear Power Amplifier

A new discrete‐amplitude pulse width modulation (DAPWM) scheme for a high‐efficiency linear power amplifier is proposed. A radio frequency (RF) input signal is divided into an envelope and a phase modulated carrier. The low‐frequency envelope is modulated so that it can be represented by a pulse whose area is proportional to its amplitude. The modulated pulse has at least two different pulse amplitude levels in order that the duty ratios of the pulse are kept large for small input. Then, an RF pulse train is generated by mixing the modulated envelope with the phase modulated carrier. The RF pulse train is amplified by a switching‐mode power amplifier, and the original RF input signal is restored by a band pass filter. Because duty ratios of the RF pulse train are kept large in spite of a small input envelope, the DAPWM technique can reduce loss from harmonic components. Furthermore, it reduces filtering efforts required to suppress harmonic components. Simulations show that the overall efficiency of the pulsed power amplifier with DAPWM is about 60.3% for a mobile WiMax signal. This is approximately a 73% increase compared to a pulsed power amplifier with PWM.     

Enhancement of Thermopower of TAGS‐85 High‐Performance Thermoelectric Material by Doping with the Rare Earth Dy

Enhancement of thermopower is achieved by doping the narrow‐band semiconductor Ag_6.52Sb_6.52Ge_36.96Te₅₀ (acronym TAGS‐85), one of the best p‐type thermoelectric materials, with 1 or 2% of the rare earth dysprosium (Dy). Evidence for the incorporation of Dy into the lattice is provided by X‐ray diffraction and increased orientation‐dependent local fields detected by ¹²⁵Te NMR spectroscopy. Since Dy has a stable electronic configuration, the enhancement cannot be attributed to 4f‐electron states formed near the Fermi level. It is likely that the enhancement is due to a small reduction in the carrier concentration, detected by ¹²⁵Te NMR spectroscopy, but mostly due to energy filtering of the carriers by potential barriers formed in the lattice by Dy, which has large both atomic size and localized magnetic moment. The interplay between the thermopower, the electrical resistivity, and the thermal conductivity of TAGS‐85 doped with Dy results in an enhancement of the power factor (PF) and the thermoelectric figure of merit (ZT) at 730 K, from PF = 28 μW cm^?1 K^?2 and ZT ≤ 1.3 in TAGS‐85 to PF = 35 μW cm^?1 K^?2 and ZT ≥ 1.5 in TAGS‐85 doped with 1 or 2% Dy for Ge. This makes TAGS‐85 doped with Dy a promising material for thermoelectric power generation.     

High‐Efficiency Water‐Transport Channels using the Synergistic Effect of a Hydrophilic Polymer and Graphene Oxide Laminates

Graphene oxide (GO) laminates possess unprecedented fast water‐transport channels. However, how to fully utilize these unique channels in order to maximize the separation properties of GO laminates remains a challenge. Here, a bio‐inspired membrane that couples an ultrathin surface water‐capturing polymeric layer (<10 nm) and GO laminates is designed. The proposed synergistic effect of highly enhanced water sorption from the polymeric layer and molecular channels from the GO laminates realizes fast and selective water transport through the integrated membrane. The prepared membrane exhibits highly selective water permeation with an excellent water flux of over 10 000 g m^?2 h^?1, which exceeds the performance upper bound of state‐of‐the‐art membranes for butanol dehydration. This bio‐inspired strategy demonstrated here opens the door to explore fast and selective channels derived from 2D or 3D materials for highly efficient molecular separation.     

Preparation of Highly Stable Black Phosphorus by Gold Decoration for High‐Performance Thermoelectric Generators

For thermoelectric (TE) applications, the surface of exfoliated black phosphorus (BP) can be successfully functionalized with Au nanoparticles (NPs), leading to significantly enhanced TE performance for a controlled Au NP content. A facile and selective decoration of metal species on the defect sites of BP is achieved by the spontaneous formation of Au NPs on the surface of BP through a redox reaction of Au precursors. Such a heterostructure provided by the Au decoration of BP enhances electrical conductivity (from 0.001 to 63.3 S cm^?1) through tuning of the charge carrier concentration and retains the initial Seebeck coefficient of BP. Consequently, the TE power factor of the Au‐decorated BP increases significantly to 68.5 µV m^?1 K^?2, which is 2740 times that of the pristine BP. More significantly, in contrast to the severe degradation of the pristine BP in the air, surface‐functionalized BP exhibits excellent stability upon exposure to air for a long period, which is beneficial for practical TE applications. Given these interesting and unique properties of Au‐decorated BP, a vertical TE generator with a high power output of 79.3 nW (ΔT = 2 °C) is prepared by using the Au‐decorated BP as a p‐type TE material.     

High‐Performance Organic Transistor Memory Elements with Steep Flanks of Hysteresis

High‐performance organic transistor memory elements with donor‐polymer blends as buffer layers are presented. These organic memory transistors have steep flanks of hysteresis with an ON/OFF memory ratio of up to 2 × 10⁴, and a retention time in excess of 24 h. Inexpensive materials such as poly(methyl methacrylate), ferrocene and copper phthalocyanine are used for the device fabrication, providing a convenient approach of producing organic memory transistors at low cost and high efficiency.     

Robust High Thermoelectric Harvesting Under a Self‐Humidifying Bilayer of Metal Organic Framework and Hydrogel Layer

Robust thermoelectric harvesting is explored from a proton‐doped mixed ionic conductive (PMIC) film under water‐harvesting metal organic framework (MOF) film coupled with hydrogel layer (MOF/HG). As a PMIC, highly doped poly(3,4‐ethylenedioxythiophene)s with poly(styrene sulfonate) (PEDOT:PSS) is prepared by precisely controlling the proton doping to afford a stable and high thermoelectric PMIC. Among the PMICs, the PEDOT:PSS film doped with 30 wt% of poly(styrene sulfonic acid) (PSSH) recorded a Seebeck coefficient of over 16.2 mV K^?1 and a thermal voltage of 81 mV for a temperature gradient (ΔT) of 5 K. The thermal charging on PMICs afforded high thermal voltage and current output, reproducibly, to show cumulative thermoelectric nature. Environmentally sustainable thermoelectric harvesting is achieved from a PMIC under a MOF/HG, prepared by water‐harvesting MOF‐801 coupled with a HG layer, to provide constant relative humidity of 90% and V_oc over 72 h at ambient condition.     

Electron‐Transport‐Layer‐Assisted Crystallization of Perovskite Films for High‐Efficiency Planar Heterojunction Solar Cells

Crystal engineering of CH₃NH₃PbI₃ perovskite materials through template‐directed nucleation and growth on PbI₂ nuclei dispersed in a polar fullerene (C₆₀ pyrrolidine tris‐acid, CPTA) electron transport layer (ETL) (CPTA:PbI₂) is proposed as a route for controlling crystallization kinetics and grain sizes. Chemical analysis of the CPTA:PbI₂ template confirms that CPTA carboxylic acid groups can form a monodentate or bidentate chelate with Pb(II), resulting in a lower nucleation barrier that promotes rapid formation of the tetragonal perovskite phase. Moreover, it is demonstrated that a uniform CH₃NH₃PbI₃ film with highly crystalline and large domain sizes can be realized by increasing the spacing between nuclei to retard perovskite crystal growth via careful control of the preferred nucleation site distribution in the CPTA:PbI₂ layer. The improved perovskite morphology possesses a long photoluminescence lifetime and efficient photocarrier transport/separation properties to eliminate the hysteresis effect. The corresponding planar heterojunction photovoltaic yields a high power conversion efficiency (PCE) of 20.20%, with a high fill factor (FF) of 81.13%. The average PCE and FF values for 30 devices are 19.03% ± 0.57% and 78.67% ± 2.13%, respectively. The results indicate that this ETL template‐assisted crystallization strategy can be applied to other organometal halide perovskite‐based systems.     

An Empirical Analysis on a Predictive Method of Systematic Segmentation in Volatile High‐Tech Markets

High‐tech markets are unpredictable owing to rapid technology innovation, diverse customer needs, high competition, and other elements. Many scholars have attempted to explain the uncertainty in high‐tech markets using their own various approaches. However, sufficiently clear ways to predict diverse changes and trends in high‐tech markets have yet to be presented. Thus, this paper proposes a new approach model, that is, systematic market segmentation, to give more accurate information. Using an empirical dataset from the mobile handset market in the Republic of Korea, we conduct our research model consisting of three steps. First, we categorize nine basic segments. Second, we test the stability of these segments. Finally, we profile the characteristics of the customers and products. We conclude that the approach is able to offer more diagnostic information to both practitioners and scholars. It is expected to provide rich information for an appropriate marketing mix in practice.     

Systematic Study of Widely Applicable N‐Doping Strategy for High‐Performance Solution‐Processed Field‐Effect Transistors

A specific design for solution‐processed doping of active semiconducting materials would be a powerful strategy in order to improve device performance in flexible and/or printed electronics. Tetrabutylammonium fluoride and tetrabutylammonium hydroxide contain Lewis base anions, F^? and OH^?, respectively, which are considered as organic dopants for efficient and cost‐effective n‐doping processes both in n‐type organic and nanocarbon‐based semiconductors, such as poly[[N,N′‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene)] (P(NDI2OD‐T2)) and selectively dispersed semiconducting single‐walled carbon nanotubes by π‐conjugated polymers. The dramatic enhancement of electron transport properties in field‐effect transistors is confirmed by the effective electron transfer from the dopants to the semiconductors as well as controllable onset and threshold voltages, convertible charge‐transport polarity, and simultaneously showing excellent device stabilities under ambient air and bias stress conditions. This simple solution‐processed chemical doping approach could facilitate the understanding of both intrinsic and extrinsic charge transport characteristics in organic semiconductors and nanocarbon‐based materials, and is thus widely applicable for developing high‐performance organic and printed electronics and optoelectronics devices.     

Design and Architecture of Low‐Latency High‐Speed Turbo Decoders

In this paper, we propose and present implementation results of a high‐speed turbo decoding algorithm. The latency caused by (de)interleaving and iterative decoding in a conventional maximum a posteriori turbo decoder can be dramatically reduced with the proposed design. The source of the latency reduction is from the combination of the radix‐4, center to top, parallel decoding, and early‐stop algorithms. This reduced latency enables the use of the turbo decoder as a forward error correction scheme in real‐time wireless communication services. The proposed scheme results in a slight degradation in bit error rate performance for large block sizes because the effective interleaver size in a radix‐4 implementation is reduced to half, relative to the conventional method. To prove the latency reduction, we implemented the proposed scheme on a field‐programmable gate array and compared its decoding speed with that of a conventional decoder. The results show an improvement of at least five fold for a single iteration of turbo decoding.     

Precisely Controlled Microsphere Design via Visible‐Light Cross‐Linking of Functional Prepolymers

A new strategy for particle synthesis is enabled by utilizing modern synthetic, polymer, and photochemical techniques to facilitate the synthesis of highly narrow–disperse multifunctional microspheres from visible‐light induced crosslinking of prepolymers in both a single and dual polymer system. The approach requires no stabilizers, bases, or initiators, and proceeds at ambient temperature to yield microspheres with a tunable size range (0.25–5 µm) in less than 4 h, depending largely on solvent composition, but also polymer concentration (2–10 mg mL^?1), ratio, and irradiation intensity (3–20 W). Critically, the visible‐light induced dimerization reaction exploited herein enables simple functional particle syntheses via a single polymer system. Underpinned by an in‐depth kinetic analysis of the particle formation as well as a detailed small molecule study, the mechanism for particle formation is also elucidated. Importantly, inherent advantages of the system are exploited for surface functionalization of residual acrylate and hydroxyl groups (generating inherently fluorescent particles).     

Doping Dependent In‐Plane and Cross‐Plane Thermoelectric Performance of Thin n‐Type Polymer P(NDI2OD‐T2) Films

Thermoelectric generators pose a promising approach in renewable energies as they can convert waste heat into electricity. In order to build high efficiency devices, suitable thermoelectric materials, both n‐ and p‐type, are needed. Here, the n‐type high‐mobility polymer poly[N,N′‐bis(2‐octyldodecyl)naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl]‐alt‐5,5′‐(2,2′‐bithiophene) (P(NDI2OD‐T2)) is focused upon. Via solution doping with 4‐(1,3‐dimethyl‐2,3‐dihydro‐1H‐benzoimidazol‐2‐yl)‐N,N‐diphenylaniline (N‐DPBI), a maximum power factor of (1.84 ± 0.13) µW K^?2 m^?1 is achieved in an in‐plane geometry for 5 wt% dopant concentration. Additionally, UV–vis spectroscopy and grazing‐incidence wide‐angle X‐ray scattering are applied to elucidate the mechanisms of the doping process and to explain the discrepancy in thermoelectric performance depending on the charge carriers being either transported in‐plane or cross‐plane. Morphological changes are found such that the crystallites, built‐up by extended polymer chains interacting via lamellar and π–π stacking, re‐arrange from face‐ to edge‐on orientation upon doping. At high doping concentrations, dopant molecules disturb the crystallinity of the polymer, hindering charge transport and leading to a decreased power factor at high dopant concentrations. These observations explain why an intermediate doping concentration of N‐DPBI leads to an optimized thermoelectric performance of P(NDI2OD‐T2) in an in‐plane geometry as compared to the cross‐plane case.