Solution Processing Route to Multifunctional Titania Thin Films: Highly Conductive and Photcatalytically Active Nb:TiO2

This paper reports the synthesis of highly conductive niobium doped titanium dioxide (Nb:TiO₂) films from the decomposition of Ti(OEt)₄ with dopant quantities of Nb(OEt)₅ by aerosol‐assisted chemical vapor deposition (AACVD). Doping Nb into the Ti sites results in n‐type conductivity, as determined by Hall effect measurements. The doped films display significantly improved electrical properties compared to pristine TiO₂ films. For 5 at.% Nb in the films, the charge carrier concentration was 2 × 10²¹ cm^?3 with a mobility of 2 cm² V^–1 s^–1 . The corresponding sheet resistance is as low as 6.5 Ω sq^–1 making the films suitable candidates for transparent conducting oxide (TCO) materials. This is, to the best of our knowledge, the lowest reported sheet resistance for Nb:TiO₂ films synthesized by vapour deposition. The doped films are also blue in colour, with the intensity dependent on the Nb concentration in the films. A combination of synchrotron, laboratory and theoretical techniques confirmed niobium doping into the anatase TiO₂ lattice. Computational methods also confirmed experimental results of both delocalized (Ti⁴⁺) and localized polaronic states (Ti³⁺) states. Additionally, the doped films also functioned as photocatalysts. Thus, Nb:TiO₂ combines four functional properties (photocatalysis, electrical conductivity, optical transparency and blue colouration) within the same layer, making it a promising alternative to conventional TCO materials.     

BPC – A binary priority countdown protocol

In modern wireless ad hoc networks, with a high speed PHY, every collision means a significant loss of useful bandwidth. In the last few years different binary contention protocols have been introduced to address this problem. In this work we propose a novel binary contention protocol called binary priority countdown (BPC) protocol, whose goal is to reduce collisions as well as contention time. BPC uses a new priority countdown mechanism which exploits the efficiency of binary countdown, but the priority countdown process is not constrained to a single binary countdown round. This way, the priority space is not defined by the length of binary countdown round, like in other binary countdown protocols proposed in the literature, and arbitrary medium access priorities can be decremented through multiple binary countdown rounds if necessary. The ability of a new priority countdown mechanism to count down any priority number without changing the length of a binary countdown round, allows independent management of priority space. This “independence” of priority space introduces new optimization and adaptation possibilities. Collision memory effect is recognized and described. BPC protocol reveals connection between unary, binary and digit contention protocols. All three groups of protocols can now be seen as members of the same class of contention algorithms. Preliminary simulation results are shown.     

A Dendritic Nickel Cobalt Sulfide Nanostructure for Alkaline Battery Electrodes

A uniform dendritic NiCo₂S₄@NiCo₂S₄ hierarchical nanostructure of width ≈100 nm is successfully designed and synthesized. From kinetic analysis of the electrochemical reactions, those electrodes function in rechargeable alkaline batteries (RABs). The dendritic structure exhibited by the electrodes has a high discharge‐specific capacity of 4.43 mAh cm^?2 at a high current density of 240 mA cm^?2 with a good rate capability of 70.1% after increasing the current densities from 40 to 240 mA cm^?2. At low scan rate of 0.5 mV s^?1 in cyclic voltammetry test, the semidiffusion controlled electrochemical reaction contributes ≈92% of the total capacity, this value decreases to ≈43% at a high scan rate of 20 mV s^?1. These results enable a detailed analysis of the reaction mechanism for RABs and suggest design concepts for new electrode materials.     

Fast Symbol Detection for Massive G-STBC MIMO Systems

In this paper, a group-based fast symbol detection scheme is proposed for massive Group-wise Space–Time Block Code Multiple-Input Multiple-Output systems. The proposed scheme first chooses a number G, (e.g. \(G=4,6,8\)) as the size of each group and then conducts the Minimum Mean Square Error (MMSE) detectors to facilitate symbol detection group by group. In particular, instead of directly using huge computational complexity to compute the MMSE detectors, the proposed scheme recursively finds the corresponding assistant matrices to determine the groups and calculate the MMSE detectors. As a result, the transmitted symbols can be recursively estimated group by group. Finally, simulation results and complexity analysis show the proposed scheme performs very close to the existing methods, while using lower computational complexity.     

Engineering the Interlayer Spacing by Pre-Intercalation for High Performance Supercapacitor MXene Electrodes in Room Temperature Ionic Liquid

MXenes exhibit excellent capacitance at high scan rates in sulfuric acid aqueous electrolytes, but the narrow potential window of aqueous electrolytes limits the energy density. Organic electrolytes and room-temperature ionic liquids (RTILs) can provide higher potential windows, leading to higher energy density. The large cation size of RTIL hinders its intercalation in-between the layers of MXene limiting the specific capacitance in comparison to aqueous electrolytes. In this work, different chain lengths alkylammonium (AA) cations are intercalated into Ti₃C₂T_x, producing variation of MXene interlayer spacings (d-spacing). AA-cation-intercalated Ti₃C₂T_x (AA-Ti₃C₂), exhibits higher specific capacitances, and cycling stabilities than pristine Ti₃C₂T_x in 1 m 1-ethly-3-methylimidazolium bis-(trifluoromethylsulfonyl)-imide (EMIMTFSI) in acetonitrile and neat EMIMTFSI RTIL electrolytes. Pre-intercalated MXene with an interlayer spacing of ≈2.2 nm, can deliver a large specific capacitance of 257 F g⁻¹ (1428 mF cm⁻² and 492 F cm⁻³) in neat EMIMTFSI electrolyte leading to high energy density. Quasi elastic neutron scattering and electrochemical impedance spectroscopy are used to study the dynamics of confined RTIL in pre-intercalated MXene. Molecular dynamics simulations suggest significant differences in the structures of RTIL ions and AA cations inside the Ti₃C₂T_x interlayer, providing insights into the differences in the observed electrochemical behavior.     

Efficient parasitic substrate modeling for monolithic mixed-A/D circuit design and verification

Parasitic analog-digital noise coupling has been identified as a key issue facing designers of mixed-signal integrated circuits. In particular, signal crosstalk through the common chip substrate has become increasingly problematic. This paper demonstrates a methodology for developing simulation, synthesis, and verification models to analyze the global electrical behavior of the non-ideal semiconductor substrate. First, a triangular discretization method is employed to generate RC equivalent-circuit substrate models which are far less complex than those formulated by conventional techniques. The networks are then accurately approximated for subsequent analysis by an efficient reduction algorithm which uses a well-conditioned Lanczos moment-matching process. Through congruence transformations, the network admittance matrices are transformed to reduced equivalents which are easily post-processed to derive passive, SPICE-compatible netlist representations of the reduced models. The pure-RC properties of the extracted substrate networks are fully exploited to formulate an efficient overall algorithm. For validation, the strategy has been successfully applied to several mixed-signal circuit examples.     

Deconvoluting Energy Transport Mechanisms in Metal Halide Perovskites Using CsPbBr3 Nanowires as a Model System

Understanding energy transport in metal halide perovskites is essential to effectively guide further optimization of materials and device designs. However, difficulties to disentangle charge carrier diffusion, photon recycling, and photon transport have led to contradicting reports and uncertainty regarding which mechanism dominates. In this study, monocrystalline CsPbBr₃ nanowires serve as 1D model systems to help unravel the respective contribution of energy transport processes in metal-halide perovskites. Spatially, temporally, and spectrally resolved photoluminescence (PL) microscopy reveals characteristic signatures of each transport mechanism from which a robust model describing the PL signal accounting for carrier diffusion, photon propagation, and photon recycling is developed. For the investigated CsPbBr₃ nanowires, an ambipolar carrier mobility of μ = 35 cm² V⁻¹ s⁻¹ is determined, and is found that charge carrier diffusion dominates the energy transport process over photon recycling. Moreover, the general applicability of the developed model is demonstrated on different perovskite compounds by applying it to data provided in previous related reports, from which clarity is gained as to why conflicting reports exist. These findings, therefore, serve as a useful tool to assist future studies aimed at characterizing energy transport mechanisms in semiconductor nanowires using PL.     

Magnetic and Temperature‐Sensitive Release Gels from Supramolecular Polymers

Supramolecular gels consisting of trivalent polyisobutylene and bivalent poly(ethylene oxide) are generated. Strong hydrogen bonding interactions, affixed to the end‐group moieties of the respective polymers (binding constant K_assn = 10⁵ M ^–1), serve as molecular glue, leading to the formation of weak gels. Two different gels were prepared: one, with a short telechelic poly(ethylene glycol) (PEG) segment (gel A), and one with a longer PEG segment (number‐average molecular weight M_n = 2000 g mol^–1) (gel B). Both gels show a significant increase in viscosity upon mixing of the two polymeric components, with a lag time of several minutes, indicative of nucleation mechanisms as the formation principle. However, only gel A displays classical gel‐like behavior, with a loss modulus G′ larger than the storage modulus G″ after formation. Both gels display microphase‐separated behavior with a spacing between 4–5 nm as probed via small‐angle X‐ray scattering (SAXS) and transmission electron microscopy (TEM) measurements. The incorporation of magnetic nanoparticles (Fe₂O₃; radius r = 3.5 nm) is successfully achieved, generating new magnetic gels with strongly thermoresponsive properties, displaying a strong temperature‐dependent release profile of included dye molecules. Magnetic measurements indicate a superparamagnetic behavior of the incorporated nanoparticles, prospecting the application as magneto‐sensitive delivery gels for pharmaceutical purposes.     

Low-Power Log-Domain CMOS Filter Bank for 2-D Sound Source Localization

This paper proposes the design of a novel current-mode front-end for the extraction of localization spectral cues from two audio signals, together with test results. The front-end consists of two parallel filter banks, envelope extraction and comparison circuitry, together with an AGC loop. The extracted cues are intended to be further processed in order to determine the source azimuth and elevation. A current-mode log-domain implementation using subthreshold MOS operation is used for micropower operation while still achieving a good bandwidth and linearity. A current-mode solution is also preferred because of the ease of implementation of certain mathematical operations. The front-end splits the input signals into different frequency bands and computes monaural and interaural spectral cues from the resulting signal envelopes for each band. The front-end has been optimized to operate at a supply voltage of 1.8 V and most blocks have been designed using a differential architecture. To our knowledge, this is the first log-domain implementation of a front-end for 2-D localization cues extraction. The design has been carried out using a standard double-poly double-metal 0.8 m CMOS process with V _T = 0.8 V. The bandpass filters which form the main core of the chip exhibit a measured dynamic range of 62 dB corresponding to 1.9% THD, while the total power dissipation is 890 W.