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121.
The elaborate balance between the open-circuit voltage (VOC) and the short-circuit current density (JSC) is critical to ensure efficient organic solar cells (OSCs). Herein, the chalcogen containing branched chain engineering is employed to address this dilemma. Three novel nonfullerene acceptors (NFAs), named BTP-2O , BTP-O-S , and BTP-2S , featuring different peripheral chalcogen containing branched chains are synthesized. Compared with symmetric BTP-2O and BTP-2S grafting two alkoxy or alkylthio branched chains, the asymmetric BTP-O-S grafting one alkoxy and one alkylthio branched chains shows mediate absorption range, applicable miscibility, and favorable crystallinity. Benefiting from the enhanced π–π stacking and charge transport, an optimal power conversion efficiency (PCE) of 17.3% is obtained for the PM6: BTP-O-S -based devices, with a good balance between VOC (0.912 V) and JSC (24.5 mA cm−2), and a high fill factor (FF) of 0.775, which is much higher than those of BTP-2O (16.1%) and BTP-2S -based (16.4%) devices. Such a result represents one of the highest efficiencies among the binary OSCs with VOC surpassing 0.9 V. Moreover, the BTP-O-S -based devices fabricated by using green solvent yield a satisfactory PCE of 17.1%. This work highlights the synergistic effect of alkoxy and alkylthio branched chains for high-performance OSCs by alleviating voltage loss and enhancing FF.  相似文献   
122.
瞿小宇 《移动信息》2023,45(10):155-157
在信息技术高度发达的时代,船舶自动识别系统(AIS)也在逐步发展,为船舶在行驶中的安全提供了可靠的技术支持,是一种较为重要的新型航行设备。AIS和ARPA在船舶碰壁中的有效应用,需要对船舶行驶及岸边船舶信息的自动共享、追踪等,以帮助工作人员掌握船舶行驶状况。文中从船舶在行驶中的碰撞问题出发,对避碰问题进行了分析,对其在实际使用中的覆盖面及追踪信息的可靠性进行了研究、对比,从而对比两者的优缺点,并提出了相应的对策。  相似文献   
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How to accurately compensate the Doppler shift is the main challenge for broadband satellite terminals. In this paper, a frequency offset estimation algorithm based on frequency domain window function iterative peaking search is proposed with high-order M-APSK signal models, considering both algorithm complexity and estimation accuracy. The variance of the new algorithm is derived mathematically, and performance curve compared with Cramer-Rao Lower Bound (CRLB) is also simulated under various SNR (signal-to-noise ratio). The effectiveness of new method is verified by simulations.

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A high-power microsecond pulsed microwave system operating in the X-band region was used for the catalytic conversion of methane. Microwave microsecond pulses at repetition rates of 50 and 80 Hz were used to initiate chemical reactions. The Microwave-Induced Acoustic technique was employed in combination with gas chromatography for on-line detection of chemical products. Methane was converted to C2 and C3 hydrocarbons. The selectivity of ethane in hydrocarbon products can be >90 %. The contribution of hydrogen evolution and carbon deposition has been shown to be important. A comparison between previous experiments performed with millisecond pulse durations is given.  相似文献   
128.
Using 12-tungstosilicic acid (SiW124-) as the catalyst, rhodamine B (RhB) dye in an aerated aqueous solution can undergo an effective photocatalytic stepwise N-deethylation process under visible light irradiation, and dioxygen is reduced to hydrogen peroxide by the reducedSiW12 4-. This provides the potential for moving polyoxometalate-based photocatalytic processes from the near-UV into the visible region of the spectrum.  相似文献   
129.
An insoluble polystyrene-supported triflating reagent has been prepared by suspension co-polymerization of N-(4-vinylphenyl)trifluoromethanesulphonimide, styrene and the JandaJel® cross-linker. This reagent, in the presence of triethylamine, allows for the efficient synthesis of aryl triflates from a wide range of phenols in a process that permits the desired product to be isolated from the reaction mixture in essentially pure form via several filtration and concentration operations. Adding to the utility of this reagent is its ability to be easily recovered, regenerated and reused. Both soluble and insoluble bifunctional polymers containing trialkylamine moieties in addition to triflimide groups were also prepared and examined as triflating reagents. Unfortunately these reagents afforded only modest yields of the desired products in representative reactions.  相似文献   
130.
The time-resolved ESR signal of a triplet radical pair was detected upon excitation of a solid mixture of acridine and acridan at room temperature. The ZFS parameters of the triplet radical pair were determined to be D=−0.0100 cm−1 and E=0.00053 cm−1. The structure of the radical pair is discussed on the basis of the data.  相似文献   
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