Electrochemical determination of niobium cathode as an efficient electrocatalyst for hydrogen generation in acidic media

Hydrogen gas (H₂) is notified as a renewable energy carrier. It is wanted to discover a low-cost electrocatalyst for the hydrogen evolution reaction (HER) to substitute the high-cost Pt in electrolysis cell. Niobium electrocatalyst nominated to substitute noble materials for electrocatalytic H₂ production and its electrochemical manner was estimated in H₂SO₄ acid of various concentrations utilizing a steady-state polarization and electrochemical impedance spectroscopy (EIS). The influences of acid concentration, cathodic potential and temperature on the H₂ creation were examined. The outcomes display that HER on Nb electrode proceeds by the Volmer-Heyrovsky mechanism. EIS tests, under open circuit and under cathodic polarization, were performed and the fitting has been done utilizing a suggested model for the electrode/electrolyte interface. Apparent activation energies (E_a) were estimated to be ca. 10.5 kJ mol^?1 for the HER on Nb. Thus, Nb is a good electrocatalyst for the cathodic H₂ manufacturing.     

Revealing Electrical-Poling-Induced Polarization Potential in Hybrid Perovskite Photodetectors

Despite recent rapid advances in metal halide perovskites for use in optoelectronics, the fundamental understanding of the electrical-poling-induced ion migration, accounting for many unusual attributes and thus performance in perovskite-based devices, remain comparatively elusive. Herein, the electrical-poling-promoted polarization potential is reported for rendering hybrid organic–inorganic perovskite photodetectors with high photocurrent and fast response time, displaying a tenfold enhancement in the photocurrent and a twofold decrease in the response time after an external electric field poling. First, a robust meniscus-assisted solution-printing strategy is employed to facilitate the oriented perovskite crystals over a large area. Subsequently, the electrical poling invokes the ion migration within perovskite crystals, thus inducing a polarization potential, as substantiated by the surface potential change assessed by Kelvin probe force microscopy. Such electrical-poling-induced polarization potential is responsible for the markedly enhanced photocurrent and largely shortened response time. This work presents new insights into the electrical-poling-triggered ion migration and, in turn, polarization potential as well as into the implication of the latter for optoelectronic devices with greater performance. As such, the utilization of ion-migration-produced polarization potential may represent an important endeavor toward a wide range of high-performance perovskite-based photodetectors, solar cells, transistors, scintillators, etc.     

Corrosion behaviour and mechanism of 6082 aluminium alloy in NaCl and Na2SO4 etchants

The corrosion behaviour of 6082 aluminium alloy was studied by measuring the electrochemical impedance spectra and electrode polarization curves. After the electrochemical tests, a microstructural analysis of the samples was conducted by using optical microscopy and electron scanning microscopy techniques to determine the corrosion mechanism. The results show that the Nyquist plot of the electrochemical impedance data in the NaCl solution consists of high- and low-frequency capacitive impedance loops. When ions are added to the NaCl etchant, the Nyquist plots of the electrochemical impedance data are composed of two different curves: a high-frequency capacitive impedance loop and a low-frequency inductive impedance loop. The corrosion current density increases with increasing concentration, and as a result, the corrosion resistance of the aluminium alloy decreases. The microstructures of 6082 aluminium alloy consist of Mg₂Si secondary particles in a large α-Al matrix. Pitting corrosion initially occurs at the boundary between the matrix and secondary particles because the electrode potentials of the matrix and secondary particles are different. Then, corrosion paths develop along the network-like grain boundaries, and finally, massive network-like corrosion occurs throughout the entire alloy.     

SCMA场景下的极化码编解码方案改进研究

极化码是目前唯一一种被证明可达到信道容量的编码方式,稀疏码分多址接入(Sparse Code Division Multiple Access,SCMA)可以提高频谱资源的利用率和接入系统的用户接入数量。为了提升SCMA与极化码的联合系统的误码率性能和译码时延,使联合系统的应用越来越广泛,提出了2种降低译码复杂度的方式:简化的左信息更新方式和剪枝译码算法。简化的左信息更新方式对于N=256,N=1024的极化码分别能降低37.6%和44.6%的存储资源占用数;剪枝译码算法在码率为0.5时能降低50%左右的计算复杂度。基于简化的SCAN算法改进了联合检测译码算法,在接收机采用外循环迭代的结构,引入了阻尼机制,选取最优的阻尼方式和最优阻尼值。仿真分析了所提联合检测译码算法与原有联合检测译码算法的误码率性能差异,外迭代接收机性能与内外双循环迭代的接收机性能相同,采用阻尼机制联合接收机的性能比无阻尼接收机的性能高0.8 dB左右,SJIDD的误帧率性能比保留宽度为32的SCLJDD的性能低0.7 dB左右,但能使接收机处理时延降至原来的1/4~1/8。     

Corrosion of Mg alloys EV31A,WE43B,and ZE41A in chloride- and sulfate-containing solutions saturated with magnesium hydroxide

This study studied corrosion in 0.1 M Na₂SO₄, 0.1 M NaCl, and 0.6 M NaCl, all saturated with Mg(OH)₂, using weight loss, hydrogen evolution, and electrochemical measurements. Corrosion was similar in all cases. Nevertheless, the corrosion rates were alloy-dependent, were somewhat lower in 0.1 M Na₂SO₄ than in 0.1 M NaCl, and increased with NaCl concentration. The corrosion damage morphology was similar for all solutions; the extent correlated with the corrosion rate. The corrosion rates evaluated by the electrochemical methods were lower than those evaluated from hydrogen evolution, consistent with the Mg corrosion mechanism involving the unipositive Mg⁺ ion.     

A minimalist approach to polarization resistance measurements in a reinforced concrete structure

In the curriculum of future civil engineers, electrochemical concepts are often neglected, even though this knowledge is essential to adequately maintain reinforced concrete structures in a chloride-exposed environment. Experiments are necessary to consolidate key theoretical concepts, but laboratory experience often involves complex and expensive electronic equipment that may obscure the basic procedures at work. This paper presents a simple minimalistic electrochemical test for polarization resistance measurements by which students can learn basic concepts of corrosion electrochemistry and estimate the corrosion rate as a key parameter for estimation of the remaining service life of concrete structures. The focus is on avoiding unnecessary complications and providing an experiment that can be readily implemented for a wider student reach.     

可重构智能表面辅助的四元数调制无线通信系统

四元数调制(Quaternion Modulation,QMod)是一种新型高传输速率的极化调制(Polarized Modulation,PMod)技术,是未来卫星通信系统中极具潜力的多元调制方案之一。QMod将数据块分成4块,其中两块是传输数据信号,另外两块则映射到极化状态部分。每个极化状态块均有一位比特,那么它们可以产生4个极化状态组合。这些状态组合可以用来确定传输数据块在四元数4个不同维度中的位置,从而获得两位额外的传输比特。相比于传统的PMod技术,QMod有着更高的频谱效率。为了进一步挖掘QMod的潜力,介绍了由可重构智能表面(Reconfigurable Intelligent Surface,RIS)辅助的QMod系统,同时推导了该系统的平均误码率理论上界,并在瑞利信道下进行了BER性能仿真。仿真结果表明,RIS辅助的PMod或者QMod系统即便在较低的SNR情况下仍有良好的BER性能,并且随着RIS单元数的增多,其BER性能会逐步提升。     

Microwave Absorption of Crystalline Fe/MnO@C Nanocapsules Embedded in Amorphous Carbon

Crystalline Fe/MnO@C core–shell nanocapsules inlaid in porous amorphous carbon matrix(FMCA)was synthesized successfully with a novel confinement strategy.The heterogeneous Fe/MnO nanocrystals are with approximate single-domain size which gives rise to natural resonance in 2–18 GHz.The addition of MnO2 confines degree of graphitization catalyzed by iron and contributes to the formation of amorphous carbon.The heterogeneous materials composed of crystalline–amorphous structures disperse evenly and its density is significantly reduced on account of porous properties.Meanwhile,adjustable dielectric loss is achieved by interrupting Fe core aggregation and stacking graphene conductive network.The dielectric loss synergistically with magnetic loss endows the FMCA enhanced absorption.The optimal reflection loss(RL)is up to−45 dB,and the effective bandwidth(RL<−10 dB)is 5.0 GHz with 2.0 mm thickness.The proposed confinement strategy not only lays the foundation for designing high-performance microwave absorber,but also offers a general duty synthesis method for heterogeneous crystalline–amorphous composites with tunable composition in other fields.     

Preparation of Ni–P–La alloy as a novel electrocatalysts for hydrogen evolution reaction

Ternary Ni–P–La alloy was synthesized by the co-electrodeposition method on the copper substrate. The energy-dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), and X-ray diffraction (XRD) were used for characterization of the synthesized alloy. The electrochemical performance of the novel alloy was investigated based on electrochemical data obtained from steady-state polarization, Tafel curves, linear sweep voltammetry (LSV), and electrochemical impedance spectroscopy (EIS) in alkaline solution and at ambient temperature. The results showed that the microstructural properties play a vital purpose in determining the electrocatalytic activity of the novel alloys. Also, the HER on investigated alloys was performed via the Volmer-Heyrovsky mechanism and Volmer step as RDS in this work. Ni–P–La catalyst was specified by ƞ₂₅₀ = −139.0 mV, b = −93.0 mV dec⁻¹, and j_o = −181.0 μA cm⁻². The results revealed that the Ni–P–La catalysts have a high potential for HER electrocatalysts in 1M NaOH solution.