HVDC/GIC型直流偏磁的差异性分析

考虑到地磁感应电流(geomagnetically induced current, GIC)具有低频性,过去一直将其近似等效为高压直流输电(high voltage direct current, HVDC)诱发的不平衡电流进行研究。然而,与HVDC型直流偏磁相比,GIC型直流偏磁具有显著的随机性与时变性,因此简单地将两者完全等效处理并不合理,在特定场景下应加以区分。为此,首先,从理论上分析了两种类型直流偏磁在诱发原因及特点上的差异。其次,通过研究直流偏磁对变压器本体以及电流互感器的不利影响,进一步探究两种类型直流偏磁对电网一/二次设备的影响差异,为后续的偏磁治理提供有效参考。最后,基于PSCAD/EMTDC仿真平台搭建了等效仿真模型,并通过仿真验证了理论分析的正确性。     

The Heterointerface between Fe1/NC and Selenides Boosts Reversible Oxygen Electrocatalysis

The rational design and construction of efficient and inexpensive bifunctional oxygen electrocatalysts are highly desirable for the development of rechargeable Zn–air batteries (ZABs). Although single-atom Fe sites anchored on N-doped carbon catalysts (Fe₁/NC) ensure high oxygen reduction reaction activity, their unitary atomically dispersed active center faces difficult condition in catalyzing oxygen evolution reaction simultaneously. Herein, a composite catalyst containing heterointerface between Fe₁/NC and selenides ((Fe,Co)Se₂) is constructed. The obtained (Fe,Co)Se₂@Fe₁/NC exhibits extremely narrow potential gap of 0.616 V and remarkable stability in alkaline media, outperforming the benchmark catalysts (Pt/C+RuO₂: 0.720 V). Experimental results and density functional theory calculations reveal that heterointerface between Fe₁/NC and (Fe,Co)Se₂ accelerates the electron transfer and provides more moderate adsorption sites, which endow (Fe,Co)Se₂@Fe₁/NC with extremely high bifunctional oxygen catalytic activity. This study not only provides a superior bifunctional catalyst for ZABs, but also enriches the application of single-atom catalysts in multifunctional energy storage and conversion devices.     

GM2NAS: multitask multiview graph neural architecture search

Knowledge and Information Systems - Graph neural network-based multitask learning models on multiview graphs have achieved acceptable results in different real-world applications. However,...     

A weighted ADI scheme with variable time steps for diffusion-wave equations

Calcolo - We present a local projection stabilization for the virtual element discretization of the nonlinear convection–diffusion–reaction equation. We consider a...     

A Self-Assembled Vertical-Gradient and Well-Dispersed MXene Structure for Flexible Large-Area Perovskite Modules

Advancing hole transport layers (HTL) to realize large-area, flexible, and high-performance perovskite solar cells (PSCs) is one of the most challenging issues for its commercialization. Here, a self-assembled gradient Ti₃C₂T_x MXene incorporated PEDOT:PSS HTL is demonstrated to achieve high-performance large-area PSCs by establishing half-caramelization-based glucose-induced MXene redistribution. Through this process, the Ti₃C₂T_x MXene nanosheets are spontaneously dispersed and redistributed at the top region of HTL to form the unique gradient distribution structure composed of MXene:Glucose:PEDOT:PSS (MG-PEDOT). These results show that the MG-PEDOT HTL not only offers favorable energy level alignment and efficient charge extraction, but also improves the film quality of perovskite layer featuring enlarged grain size, lower trap density, and longer carrier lifetime. Consequently, the power conversion efficiency (PCE) of the flexible device based on MG-PEDOT HTL is increased by 36% compared to that of pristine PEDOT:PSS HTL. Meanwhile, the flexible perovskite solar minimodule (15 cm² area) using MG-PEDOT HTL achieve a PCE of 17.06%. The encapsulated modules show remarkable long-term storage stability at 85 °C in ambient air (≈90% efficiency retention after 1200 h) and enhanced operational lifetime (≈90% efficiency retention after 200 h). This new approach shows a promising future of the self-assembled HTLs for developing optoelectronic devices.     

Pre-Activation of CO2 at Cobalt Phthalocyanine-Mg(OH)2 Interface for Enhanced Turnover Rate

Cobalt phthalocyanine (CoPc) anchored on heterogeneous scaffold has drawn great attention as promising electrocatalyst for carbon dioxide reduction reaction (CO₂RR), but the molecule/substrate interaction is still pending for clarification and optimization to maximize the reaction kinetics. Herein, a CO₂RR catalyst is fabricated by affixing CoPc onto the Mg(OH)₂ substrate primed with conductive carbon, demonstrating an ultra-low overpotential of 0.31 ± 0.03 V at 100 mA cm⁻² and high faradaic efficiency of >95% at a wide current density range for CO production, as well as a heavy-duty operation at 100 mA cm⁻² for more than 50 h in a membrane electrode assembly. Mechanistic investigations employing in situ Raman and attenuated total reflection surface-enhanced infrared absorption spectroscopy unravel that Mg(OH)₂ plays a pivotal role to enhance the CO₂RR kinetics by facilitating the first-step electron transfer to form anionic *CO₂⁻ intermediates. DFT calculations further elucidate that introducing Lewis acid sites help to polarize CO₂ molecules absorbed at the metal centers of CoPc and consequently lower the activation barrier. This work signifies the tailoring of catalyst-support interface at molecular level for enhancing the turnover rate of CO₂RR.     

Phase-Separated Polyzwitterionic Hydrogels with Tunable Sponge-Like Structures for Stable Solar Steam Generation

Solar steam generation (SSG) through hydrogel-based evaporators has shown great promise for freshwater production. However, developing hydrogel-based evaporators with stable SSG performance in high-salinity brines remains challenging. Herein, phase-separated polyzwitterionic hydrogel-based evaporators are presented with sponge-like structures comprising interconnected pores for stable SSG performance, which are fabricated by photopolymerization of sulfobetaine methacrylate (SBMA) in water-dimethyl sulfoxide (DMSO) mixed solvents. It is shown that driven by competitive adsorption, the structures of the resulting poly(sulfobetaine methacrylate) (PSBMA) hydrogels can be readily tuned by the volume ratio of DMSO to achieve phase separation. The optimized phase-separated PSBMA hydrogels, combining the unique anti-polyelectrolyte effects of polyzwitterionic hydrogels, demonstrate a rapid water transport capability in brines. After introducing photothermal polypyrrole particles on the surface of the phase-separated PSBMA hydrogel evaporators, a stable water evaporation rate of ≈2.024 kg m⁻² h⁻¹ and high solar-to-vapor efficiency of ≈97.5% in a 3.5 wt.% brine are obtained under simulated solar light irradiation (1.0 kW m⁻²). Surprisingly, the evaporation rates remain stable even under high-intensity solar irradiation (2.0 kW m⁻²). It is anticipated that the polyzwitterionic hydrogel evaporators with sponge-like porous structures will contribute to developing SSG technology for high-salinity seawater applications.     

Modulating Backbone Conjugation of Polymeric Thermally Activated Delayed Fluorescence Emitters for High-Efficiency Blue OLEDs

Blue conjugated polymers-based OLEDs with both high efficiency and low efficiency roll-off are under big challenge. Herein, a strategy of local conjugation is proposed to construct high-efficiency blue-emitting conjugated polymers, in which the conjugation degree of polymeric backbones is adjusted by inserting different spacers. In this way, the energy level of triplet state and the energy transfer direction of the polymeric main-chains can be effectively regulated. Benefiting from such fine regulation, the prepared alternative copolymers Alt-PB36 with local conjugated main-chains can better suppress the accumulation of long-lived triplet excitons comparing with the complete conjugated polymers. The higher PLQY of Alt-PB36 also verifies the effective energy transfer from the polymeric main-chains to the TADF units. Accordingly, Alt-PB36 based solution-processed OLEDs achieve an EQE_max of 11.6% and a very low efficiency roll-off of 2.8% at 100 cd m⁻² and 15.2% at 500 cd m⁻². This result represents the best efficiency among blue light-emitting conjugated polymer-based OLEDs so far under high luminance.     

基于平面电容的油水多界面检测方法研究

含水量是衡量原油质量的重要指标,在原油的生产和储运过程中油水混合液分界面不断变化,因此全过程都要用到高精度传感器对其进行界面检测。基于电容边缘效应设计了一种侵入式平面电容传感器,其主要结构由基板和平面电极阵列两部分组成。运用有限元软件建立8电极阵列传感器模型,对不同电极工作时的电场分布进行研究,分析了平面电容传感器的检测灵敏度和成像精度。并且,研究了电极宽度、长度和相邻间距对传感器灵敏场分布的影响。对介电分布进行图像重建,使设计的平面电容阵列传感器可以检测3个分界面的高度,且经过尺寸参数优化,提高了传感器的成像精度。实验证明,运用平面电容阵列检测油水界面的方法具有可行性和有效性。     

基于双 AWG 的新型 FBG 连续解调方法研究

为了实现基于阵列波导光栅(arrayed waveguide grating, AWG)的光纤布拉格光栅(fiber Bragg gratin, FBG)的连续解调, 提出了一种使用两个 AWG 联合解调的方法。 在一个 AWG 相邻两通道光谱中间插入另一个 AWG 对应通道的光谱,组成最小 的光谱周期;每次测量均从三通道中选择光强度最强的两个通道,利用相对光强解调算法,根据其波长—功率关系对 FBG 中心 波长进行精确测量。 使用两个 100 GHz 的 AWG 搭建了实验平台,并对温度传感器的解调进行研究。 实验表明,在 0. 8 nm 的系 统最小动态范围周期内,实现了对 FBG 的连续精确解调,系统的解调线性度达 0. 999 1,波长精度达±4 pm。 对数据和实验结果 进行数学分析,可以将 C 波段范围分成多个波长周期,系统可以实现在 C 波段 40 nm 全周期范围内对单个 FBG 的连续解调。 该方法不但可以实现在 C 波段范围内基于 AWG 对 FBG 的连续解调,使得运用 FBG 可以连续感测外界物理量变化,提高了系 统的实用性。 而且,该方法能够准确解调出波长信息,为实现对 FBG 的连续精确解调提供了借鉴信息,有利于进一步扩大 FBG 的应用领域。