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991.
为了保证合环操作的顺利进行,提出了一种10 kV配电网的合环电流计算方法,重点对合环冲击电流计算过程进行改进,将最大电流出现时刻和所在相纳入考虑。首先,通过理论分析推导,介绍了所提的10 kV配电网合环前稳态电流和合环冲击电流的计算方法;然后,给出了合环操作判定条件的流程;最后,基于MATLAB/Simulink搭建了10 kV配电网的合环仿真模型,对理论分析进行了仿真验证。仿真结果表明,提出的计算方法具有较高的准确性,对实际工程中合环电流计算和合环操作判定具有一定的指导意义。 相似文献
992.
紧耦合阵列天线(Tightly Coupled Array, TCA)具有超宽带、低剖面、宽角扫描等特点,近年来受到国内外学者的广泛关注。然而,在甚高频(VHF)、特高频(UHF)频段TCA 由于馈电网络设计困难等原因现有的研究报道很少。为了填补这一空白,本文设计并测试了一款变压器巴伦馈电的TCA,利用变压器巴伦解决了单元平衡馈电困难问题,同时采用短路枝节抑制E面共模谐振,采用频率选择表面(FSS)匹配层改善宽角扫描阻抗匹配。实测结果表明,该天线在110~520 MHz 频带内、±40°扫描角范围内电压驻波比<2.5,和仿真结果吻合。 相似文献
993.
Ying-Xia Du Qiao Yang Wang-Ting Lu Qing-Yu Guan Fei-Fei Cao Geng Zhang 《Advanced functional materials》2023,33(27):2300895
Single metal atom isolated in nitrogen-doped carbon materials (M N C) are effective electrocatalysts for oxygen reduction reaction (ORR), which produces H2O2 or H2O via 2-electron or 4-electron process. However, most of M N C catalysts can only present high selectivity for one product, and the selectivity is usually regulated by complicated structure design. Herein, a carbon black-supported Co N C catalyst (CB@Co N C) is synthesized. Tunable 2-electron/4-electron behavior is realized on CB@Co-N-C by utilizing its H2O2 yield dependence on electrolyte pH and catalyst loading. In acidic media with low catalyst loading, CB@Co N C presents excellent mass activity and high selectivity for H2O2 production. In flow cell with gas diffusion electrode, a H2O2 production rate of 5.04 mol h−1 g−1 is achieved by CB@Co N C on electrolyte circulation mode, and a long-term H2O2 production of 200 h is demonstrated on electrolyte non-circulation mode. Meanwhile, CB@Co N C exhibits a dominant 4-electron ORR pathway with high activity and durability in pH neutral media with high catalyst loading. The microbial fuel cell using CB@Co N C as the cathode catalyst shows a peak power density close to that of benchmark Pt/C catalyst. 相似文献
994.
Shiyu Huang Yuan Chang Zhuwei Li Jiaqi Cao Yurou Song Junfeng Gao Licheng Sun Jungang Hou 《Advanced functional materials》2023,33(21):2211631
Photoredox catalysis is a green solution for organics transformation and CO2 conversion into valuable fuels, meeting the challenges of sustainable energy and environmental concerns. However, the regulation of single-atomic active sites in organic framework not only influences the photoredox performance, but also limits the understanding of the relationship for photocatalytic selective organic conversion with CO2 valorization into one reaction system. As a prototype, different single-atomic metal (M) sites (M2+ = Fe2+, Co2+, Ni2+, Cu2+, and Zn2+) in hydrogen-bonded organic frameworks (M-HOF) backbone with bridging structure of metal-nitrogen are constructed by a typical “two-in-one” strategy for superior photocatalytic C N coupling reactions integrated with CO2 valorization. Remarkably, Zn-HOF achieves 100% conversion of benzylamine oxidative coupling reactions, 91% selectivity of N-benzylidenebenzylamine and CO2 conversion in one photoredox cycle. From X-ray absorption fine structure analysis and density functional theory calculations, the superior photocatalytic performance is attributed to synergic effect of atomically dispersed metal sites and HOF host, decreasing the reaction energy barriers, enhancing CO2 adsorption and forming benzylcarbamic acid intermediate to promote the redox recycle. This work not only affords the rational design strategy of single-atom active sites in functional HOF, but also facilitates the fundamental insights upon the mechanism of versatile photoredox coupling reaction systems. 相似文献
995.
Leitao Cao Chao Ye Hao Zhang Shuo Yang Yicheng Shan Zhuochen Lv Jing Ren Shengjie Ling 《Advanced functional materials》2023,33(27):2301404
Ionotronic artificial motion and tactile receptor (i-AMTR) is essential to realize an interactive human-machine interface. However, an i-AMTR that effectively mimics the composition, structure, mechanics, and multi-functionality of human skin, called humanoid i-AMTR, is yet to be developed. To bridge this technological gap, this study proposes a strategy that combines molecular structure design and function integration to construct a humanoid i-AMTR. Herein, a silk fibroin ionoelastomer (SFIE) with double cross-linked molecular structure is designed to mimic the composition and structure of human skin, thereby resolving the conflict of stretchability, softness, and resilience, suffered by many previously reported ionotronics. Functionally, electromechanical sensing and triboelectricity-based tactile perception are integrated into SFIE, to enable simultaneous perception of both motion and tactile inputs. By further leveraging the machine learning and Internet of Things (IoT) techniques, the proposed SFIE-based humanoid i-AMTR precisely senses the movement of human body and accurately sortball objects made of different materials. Notably, the success rate for 610 sorting tests reaches as high as 92.3%. These promising results essentially demonstrate a massive potential of humanoid i-AMTR in the fields of sorting robots, rehabilitation medicine, and augmented reality. 相似文献
996.
Heng Zhao Jingwei Xue Hongbo Wu Baojun Lin Yuhang Cai Ke Zhou Daqin Yun Zheng Tang Wei Ma 《Advanced functional materials》2023,33(5):2210534
The power conversion efficiency (PCE) of organic solar cells (OSCs) has reached high values of over 19%. However, most of the high-efficiency OSCs are fabricated by spin-coating with toxic solvents and the optimal photoactive layer thickness is limited to 100 nm, limiting practical development of OSCs. It is a great challenge to obtain ideal morphology for high-efficiency thick-film OSCs when using non-halogenated solvents due to the unfavorable film formation kinetics. Herein, high-efficiency ternary thick-film (300 nm) OSCs with PCE of 15.4% based on PM6:BTR-Cl:CH1007 are fabricated by hot slot-die coating using non-halogenated solvent (o-xylene) in the air. Compared to PM6:BTR-Cl:Y6 blends, the stronger pre-aggregation of CH1007 in solution induces the earlier aggregation of CH1007 molecules and longer aggregation time, and thus results in high and balanced crystallinity of donors and acceptor in CH1007-based ternary film, which led to high-carrier mobility and suppressed charge recombination. The ternary strategy is further used to fabricate high-efficiency, thick-film, large-area, and flexible devices processed from non-halogenated solvents, paving the way for industrial development of OSCs. 相似文献
997.
Hai-Yang Chen Zuan-Yu Chen Min Mao Yu-Yue Wu Fan Yang Li-Xiu Gong Li Zhao Cheng-Fei Cao Pingan Song Jie-Feng Gao Guo-Dong Zhang Yong-Qian Shi Kun Cao Long-Cheng Tang 《Advanced functional materials》2023,33(48):2304927
Polydimethylsiloxanes (PDMS) foam as one of next-generation polymer foam materials shows poor surface adhesion and limited functionality, which greatly restricts its potential applications. Fabrication of advanced PDMS foam materials with multiple functionalities remains a critical challenge. In this study, unprecedented self-adhesive PDMS foam materials are reported with worm-like rough structure and reactive groups for fabricating multifunctional PDMS foam nanocomposites decorated with MXene/cellulose nanofiber (MXene/CNF) interconnected network by a facile silicone foaming and dip-coating strategy followed by silane surface modification. Interestingly, such self-adhesive PDMS foam produces strong interfacial adhesion with the hybrid MXene/CNF nano-coatings. Consequently, the optimized PDMS foam nanocomposites have excellent surface super-hydrophobicity (water contact angle of ≈159o), tunable electrical conductivity (from 10−8 to 10 S m−1), stable compressive cyclic reliability in both wide-temperature range (from −20 to 200 oC) and complex environments (acid, sodium, and alkali conditions), outstanding flame resistance (LOI value of >27% and low smoke production rate), good thermal insulating performance and reliable strain sensing in various stress modes and complex environmental conditions. It provides a new route for the rational design and development of advanced PDMS foam nanocomposites with versatile multifunctionalities for various promising applications such as intelligent healthcare monitoring and fire-safe thermal insulation. 相似文献
998.
Xin Ding Run Jiang Jialin Wu Minghui Xing Zelong Qiao Xiaofei Zeng Shitao Wang Dapeng Cao 《Advanced functional materials》2023,33(47):2306786
Developing low-cost and high-efficient bifunctional catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is greatly significant for water electrolysis. Here, Ni3N-CeO2/NF heterostructure is synthesized on the nickel foam, and it exhibits excellent HER and OER performance. As a result, the water electrolyzer based on Ni3N-CeO2/NF bifunctional catalyst only needs 1.515 V@10 mA cm−2, significantly better than that of Pt/C||IrO2 catalysts. In situ characterizations unveil that CeO2 plays completely different roles in HER and OER processes. In situ infrared spectroscopy and density functional theory calculations indicate that the introduction of CeO2 can optimizes the structure of interface water, and the synergistic effect of Ni3N and CeO2 improve the HER activity significantly, while the in situ Raman spectra reveal that CeO2 accelerates the reconstruction of OV (oxygen vacancy)-rich NiOOH for boosting OER. This study clearly unlocks the different catalytic mechanisms of CeO2 for boosting the HER and OER activity of Ni3N for water splitting, which provides the useful guidance for designing the high-performance bifunctional catalysts for water splitting. 相似文献
999.
Mei Yang Kean Chen Hui Li Yuliang Cao Hanxi Yang Xinping Ai 《Advanced functional materials》2023,33(47):2306828
Many organic solvents have excellent solution properties, but fail to serve as lithium-ion batteries (LIBs) electrolyte solvents, due to their electrochemical incompatibility with graphite anodes. Herein, a new strategy is proposed to address this issue by introducing a surface-adsorbed molecular layer to regulate the interfacial solvation structure without the alteration of electrolyte composition and properties. As a proof-of-concept study, it is demonstrated for the first time that the intrinsically incompatible propylene carbonate (PC)-based electrolyte becomes completely compatible with graphite anodes by introducing a layer of adsorbed hexafluorobenzene (HFB) molecules to weaken the Li+-PC coordination strength and facilitate the interfacial desolvation process. As a consequence, the graphite/ NCM811 pouch cells using the PC-based electrolyte containing only 1 vol.% HFB demonstrate excellent long-term cycling stabilities over 1150 cycles. This strategy is also proved to be applicable to other ethylene carbonate (EC)–free electrolytes, thus providing a new avenue for developing advanced LIB electrolytes. 相似文献
1000.
Sealed-bid auctions are a vital transaction tool in the e-commerce field. Traditional centralized auction schemes typically result in severe threats to data integrity,information transparency,and traceability owing to their excessive reliance on third parties,and blockchain-based auction schemes generally suffer from high storage costs and are deficient in functional and architectural design. To solve these problems,this study presents a sealed-bid auction scheme that removes the third-party bas... 相似文献