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1.
《International Journal of Hydrogen Energy》2022,47(61):25769-25779
Gas diffusion layer (GDL) is one of the most important components of fuel cells. In order to improve the fuel cell performance, GDL has developed from single layer to dual layers, and then to multiple layers. However, dual or multi layers in GDL are usually prepared by layer-by-layer methods, which cost too much time, energy, and resources. In this work, we successfully developed a facile one-step method to prepare a GDL with three functional layers by utilizing the different sedimentation rates and filtration rates of short carbon fiber (CF) and carbon nanotube (CNT). The treatment temperature for this GDL is much lower than that of traditional method. The thickness of the GDL can be effectively controlled from as thin as 50 μm to more than 200 μm by simply adjusting the content of CF. The GDL with high flexibility is suitable to develop high performance flexible electronics. The fuel cell with the GDL has the maximum power density 1021 mW cm?2, which shows 19% improvement comparing to the conventional one. Therefore, this work breaks the traditional concept that GDL for fuel cells only can be prepared by very complex and high-cost procedure. 相似文献
2.
《International Journal of Hydrogen Energy》2022,47(92):39204-39214
In this work, the SnS2 nanoflowers (SnS2 NFs) were solvothermally prepared in the solvent of ethanol, while SnS2 nanoplates (SnS2 NPs) were obtained through the identical conditions except for the solvent of water. The flowers were assembled with numerous nanosheets with very thin thickness, and the NPs exhibited hexagonal shape. When used as the battery-type electrode material for supercapacitors, the SnS2 NFs delivered a specific capacity of as high as 264.4 C g?1 at 1 A g?1, which was higher than the 201.6 C g?1 of SnS2 NPs. Furthermore, a hybrid supercapacitor (HSC) was assembled with the SnS2 as positive electrode and activated carbon (AC) as negative electrode, respectively. The SnS2 NFs//AC HSC exhibited a high energy density of 28.1 Wh kg?1 at 904.3 W kg?1, which was higher than the 24.2 Wh kg?1 at 844.3 W kg?1 of SnS2 NPs//AC HSC. Especially, when the power density was enhanced to the highest value of 8666.8 W kg?1, the NFs-based device could still hold 20.4 Wh kg?1. In addition, both HSC devices showed an excellent cycling stability after 5000 cycles at 5 A g?1. The present method is simple and can be extended to the preparation of other transition metal sulfides (TMSs)-based electrode materials with brilliant electrochemical performance for supercapacitors. 相似文献
3.
《Ceramics International》2022,48(15):21317-21326
1T phase molybdenum disulfide (1T-MoS2) has aroused extensive concern in energy storage devices such as supercapacitors due to its large interlayer spacing, high conductivity and good hydrophilicity. However, it is struggle to synthesize 1T-MoS2 with stable 1T phase with high content. Herein, Ammonium ion intercalation molybdenum disulfide (A-MoS2) with high 1T content and stable 3D microsphere structure was successfully synthesized using a facile hydrothermal method. We explained the feasibility of ammonium ion (NH4+) intercalation through density functional theory (DFT) calculations and proved the successful intercalation of NH4+ by XRD and XPS. Through XPS fitting, the 1T phase content is calculated as high as 83.1%. The as-prepared A-MoS2 presents a stable 3D microsphere structure with the interlayer spacing expanded to 0.93 nm, which provides a wide ion diffusion channel that allows ions to pass through quickly. Moreover, the high 1T content increases the hydrophilicity of MoS2, thereby improving the wettability of the electrode, which contributes to the interaction between the electrolyte and electrode. In 1 M Na2SO4, A-MoS2 electrode material displays high specific capacitance of 228 F g?1 at 5 mV s?1 and retains 127 F g?1 at 80 mV s?1, which proves the good rate capability. Furthermore, the assembled α-MnO2//A-MoS2 asymmetric supercapacitor (ASC) displayed a wide operating voltage of 2.1 V. The assembled ASC displays a high energy density of 35.8 Wh?kg?1 at a power density of 525.0 W kg?1, which indicates excellent energy storage performance. 相似文献
4.
《International Journal of Hydrogen Energy》2022,47(10):6848-6859
Catalyst slurries (inks) were prepared with and without thermal treatment to determine the support/ionomer structures and interactions in the catalyst layer (CL) which impact on membrane electrode performance and durability. The thermal treatment of the ink has a nominal effect on the ionomer/support structure in which the carbon support is non-graphitised. The agglomerate/aggregate structures have a high degree of support/ionomer interface and sufficient macroporosity for water movement in the CL. This improves the membrane electrode assembly (MEA) performance, but also accelerates electrochemical carbon degradation. Thermal treatment of graphitised support-containing inks resulted in increased performance facilitated by a larger support/ionomer interface. Without thermal treatment, the more hydrophobic support would form aggregate structures in which water contact was restricted, limiting proton transfer, isolating catalyst, decreasing performance. The water limited access, would however, prolong stability during accelerates carbon degradation. The electrochemical properties were studied using full and half MEA cells. 相似文献
5.
《Ceramics International》2021,47(24):34845-34850
The interfacial delamination of electrode/ceramic multilayer structure will seriously damage the reliability of low temperature co-fired ceramic (LTCC) module in practical applications. In this work, three kinds of glasses employed in Au electrode are designed and prepared to study the abnormal expansion and delamination process in the Au/ceramic LTCC multilayer structure. The interfacial delamination in the co-fired structure is found to be attributed to the abnormal expansion of glass in respect to Au electrode at high temperature, which is originated from the enlarged closed pores during the co-firing process. This conclusion is further confirmed by co-firing the sample in a low-pressure condition. The mechanism and elimination of interfacial delamination here provides a feasible solution for the design of novel glasses in Au electrode for LTCC applications. 相似文献
6.
《Ceramics International》2021,47(24):34514-34520
In this study, ruthenium was bonded to the reduced graphene oxide in an ultrasonic bath. The aerogel of the mixture was produced at −78 °C. Structural characterization of aerogels was done with XRD and FTIR, surface characterization was performed with STEM, and elemental analysis was conducted by EDX analysis. The produced aerogel composites were transformed into electrodes on conductive Nickel foam. IviumStat, a potentiostat/galvanostat device, was used for the electrochemical characterization of the symmetrical supercapacitors. According to CV voltammograms, rGO/RuO2 aerogels' highest specific capacitance was calculated as 328.6 F g−1 at a potential scan rate of 5 mV s−1. The assembled rGO/RuO2 aerogel-based supercapacitor cell offered a high energy density value of 31.1 W h kg−1 even at the power density of 8.365 kW kg−1; this is comparable to that of lead-acid and nickel-metal hybrid batteries. 相似文献
7.
《Ceramics International》2022,48(3):3536-3543
We investigated the optical and electrical properties of Ta2O5/Ag/Ta2O5 films as functions of the thicknesses of the Ta2O5 and Ag layers. It was found that with an increase in the thicknesses of the Ta2O5 and Ag layers from 10 to 40 nm and from 12 to 24 nm, respectively, the sheet resistance, carrier concentration, electron mobility, and resistivity of the Ta2O5/Ag/Ta2O5 film varied from 2.02 to 8.95 Ω/sq, 5.74 × 1021 to 2.92 × 1022 cm–3, from 13.21 to 24.07 cm2/V·s, and from 8.89 × 10-6 to 8.24 × 10-5 Ω cm, respectively. The average transmittance (Tav) of the multilayer samples ranged from 57.18% to 93.99%, and it depended on the Ta2O5 and Ag layer thicknesses. The highest Tav of 93.99% was observed for the film with 35 nm thick Ta2O5 and 18 nm thick Ag layers, and the peak Haacke's figure of merit (157.04 × 10–3 Ω–1) was obtained for 20 nm thick Ta2O5 and 21 nm thick Ag layers. Ta2O5 (100 nm) and Ta2O5/Ag/Ta2O5 (20 nm/21 nm/20 nm) samples had optical bandgaps of 4.70 and 4.45 eV, respectively. Film Wizard simulations were conducted to understand the dependence of the transmittance of the multilayer on the thicknesses of the Ta2O5 and Ag layers, and phasor analyses were performed to determine how the transmittance of the Ta2O5/Ag/Ta2O5 (20 nm/21 nm/20 nm) film depended on the Ta2O5 layer's thickness. 相似文献
8.
Manoj Karakoti Ritu Jangra Sandeep Pandey Pawan Singh Dhapola Sunil Dhali Suman Mahendia Pramod K Singh Nanda Gopal Sahoo 《International Journal of Applied Ceramic Technology》2020,17(4):1899-1908
This study deals with the utility of mini spray dryer process to improve the dispersibility, of graphene oxide(GO) and its application for high-performance supercapacitor. Initially, the neutral solution of GO was obtained using the modified Hummer's method. After this, the prepared GO solution was processed by mini spray dryer to obtain a more purified, lighter, and dispersed form of GO which is named as spray dryer processed GO (SPGO). The SPGO thus obtained showed excellent dispersibility behavior with various solvents, which is not found in case of conventional oven drying. Furthermore, utility of SPGO and its reduced form (r-SPGO) for supercapacitor applications have been investigated. Results obtained from the cyclic voltammetry(CV) analysis, impedance, and charge-discharge behavior of supercapacitor fabricated using r-SPGO shows enhanced features. Therefore, the simple spray dried GO and its reduced form, that is, r-SPGO can be utilized as a potential candidate for the supercapacitor application. Herein, as synthesized SPGO exhibited the specific capacitance of 12.07 and 37.6 F/g with PVA-H3PO4 and 1 mol/L H3PO4, respectively, at a scan rate of 5 mV/s. On the other hand, reduced form of SPGO, that is, r-SPGO showed the specific capacitance of 27.16 and 230 F/g with PVA-H3PO4 and 1 mol/L H3PO4, respectively. 相似文献
9.
通过对电阻层析成像数据采集原理和深度学习网络的研究,提出了一种基于阵列电阻值和多层感知器深度学习网络相结合的流型识别方法。利用电阻层析成像系统中的16个电极传感器来获取流型样本数据,并构建出流型识别数据库,然后对多层感知器深度学习网络进行训练,获得可以识别不同流型的网络。实验结果表明,采用阵列电阻值结合多层感知器网络对流型进行学习和识别的方法,流型识别准确率可以达到95%,解决了流型图像生成过程与数据特征预选过程中流型特征损失的问题,流型识别性能得到了提高。 相似文献
10.