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991.
在正交频分复用(OFDM)系统中,基于遗传算法的部分传输序列(GA-PTS)技术有效地降低了 PTS 的计算复杂度,但在
改进峰值-平均功率比(PAPR)性能方面却并不理想。 为此,提出在遗传算法中嵌入模拟退火(SA)算子从而构造一种混合的遗
传模拟退火(GSA)算法,并把它应用于对 PTS 的最优相位因子进行搜索。 首先,通过对 PTS 相位因子编码形成染色体,采用随
机元素组成的染色体作为遗传算法的初始群体,并评估每个染色体的适应度值。 然后,根据适应度值选择染色体,建立染色体
的变异规则和交叉规则,对群体进行迭代进化。 最后,群体中的染色体利用退火温度进行更新,从而产生出新的下一代种群。
仿真结果说明,与 GA-PTS 方案相比,该方法不仅能降低计算负担,而且能够有效地降低 OFDM 系统 PAPR 值。 相似文献
992.
采用磷酸(H3PO4)溶液对废旧LiFePO4电池正极片在低温热解得到的粉末材料进行浸出,以铁盐溶液作为补充铁源,合成电池级磷酸铁(FePO4),并将滤液pH值调到8.0以上,得到工业级磷酸锂(Li3PO4)。通过SEM、XRD和电化学性能测试,研究热处理温度、反应原料配比与溶液pH值对回收产物形貌和性能的影响。将正极片在350℃下热解2 h分离得到的粉末加入到85℃的H3PO4溶液中,在n(P)∶n(Fe)为1.3∶1.0的条件下,制备的FePO4结晶度好。制备的电池在2.5~4.0 V充放电,0.2 C和2.0 C放电比容量最高分别达到160.2 mAh/g和150.3 mAh/g。以Li3PO4方式回收滤液中的锂元素,当p H值为10时,回收率达到90%,Li3PO4纯度在99.4%以上。 相似文献
993.
《International Journal of Hydrogen Energy》2020,45(35):17504-17516
Fabrication of an electrocatalyst with remarkable electrocatalytic activity for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is important for the production of hydrogen energy. In this study, Ni–Co–W alloy urchin-like nanostructures were fabricated by binder-free and cost-effective electrochemical deposition method at different applied current densities and HER and OER electrocatalytic activity was studied. The results of this study showed that the microstructure and morphology are strongly influenced by the electrochemical deposition parameters and the best electrocatalytic properties are obtained at the electrode created at the 20 mA.cm−2applied current density. The optimum electrode requires −66 mV and 264 mV, respectively, for OER and HER reactions for delivering the 10 mA cm−2 current density. The optimum electrode also showed negligible potential change after 10 h electrolysis at 100 mA cm−2, which means remarkable electrocatalytic stability. In addition, when this electrode used as a for full water splitting, it required only 1.58 V to create a current density of 10 mA cm−2. Such excellent electrocatalytic activity and stability can be related to the high electrochemical active surface area, being binder-free, high intrinsic electrocatalytic activity and hydrophilicity. This study introduces a simple and cost-effective method for fabricating of effective electrodes with high electrocatalytic activity. 相似文献
994.
《International Journal of Hydrogen Energy》2019,44(5):3121-3137
This study aims to evaluate the convective heat transfer enhancement of the proton exchange membrane fuel cells (PEMFC) numerically. As the higher heat transfer surfaces lead to higher heat transfer rates, a flat plate porous layer is utilized in the gas flow channel (GFC). This enhancement in heat transfer stems from the corresponding modification in the temperature and velocity profiles. The influencing parameters on these profiles are the thickness, permeability, and porosity of the GFC porous layer. After performing the simulations, the results indicate that convective heat transfer has a direct relationship with GFC porous layer's thickness and permeability. However, lower values of porosity lead to the higher Nusselt numbers. Previous investigations have also mentioned the positive impact of the microporous layer (MPL) on the water management of these fuel cells. Therefore, six different sizes of MPL and the gas diffusion layer (GDL) are utilized to evaluate their impacts on the thermal management. Results indicate that although these sizes have negligible effects on the heat transfer, Nu increases by enhancing the total size of MPL and GDL. The results also show that thicker MPLs lead to higher heat transfer rates. The evaluation of the friction factor also indicates the adverse effect of the GFC porous layer, although this undesirable effect is negligible. Finally, all the simulated values are utilized to train an artificial neural network (ANN) model with high precision. This ANN model can produce more data for sensitivity analysis and presenting respective 3D diagrams of the influencing parameters on heat transfer. 相似文献
995.
《International Journal of Hydrogen Energy》2019,44(5):2857-2867
Ni complexes are promising catalysts for water splitting. Herein, a tetranuclear nickel(II) complex with bis-[(E)-N′-(1-(pyridin-2-yl)ethylidene)]carbohydrazide (HL), was synthesized and characterized by spectroscopic methods and single crystal X-ray analysis. The complex is a tetranuclear complex and the ligands are coordinated to the metal ions in the mono-negative form, (L)- to form a tetranuclear [NiL]44+ unit. Each Ni(II) ion is six-coordinated by pyridine nitrogen, azomethine nitrogen and oxygen atoms of two perpendicular carbohydrazone ligands in the mer configuration. The complex was studied as a water-oxidizing catalyst. In the next step, the role of the Ni-based compound for water oxidation on the surface of fluorine doped tin oxide as one of the true catalysts was investigated by scanning transmission electron microscopy, scanning transmission electron microscopy, spectroelectrochemistry, and electrochemistry. The electrode after water oxidation by the complex was studied and a relation between the decomposition of the Ni complex and water-oxidation reaction was proposed. The experiments show that under water-oxidation condition in the presence of the complex, a Ni-based compound on the electrode is a candidate as a contributor to the observed catalysis. 相似文献
996.
《International Journal of Hydrogen Energy》2019,44(7):3891-3905
Residential Fuel Cell micro combined heat and power (FC-μCHP) systems can help decarburizing the energy system. In the European ene.field project, the environmental performance of FC-μCHP under different conditions was therefore evaluated by means of a comprehensive Life Cycle Assessment (LCA). Important influential factors were explored, i.e. heating demands, full load hours (FLHs) and electricity replacement mixes (ERMs). The systems were compared with a stand-alone Gas Condensing Boiler (GCB) and a heat pump (HP, only in single family homes, SFHs). For the initially assumed FLHs and the current ENTSO-E ERM, relevant environmental impacts including climate change are generally smaller for the FC-μCHPs than for the HP and the stand-alone GCB. In the setting “existing SFHs in central climate” with the highest deployment potential, GHG emission savings are higher the more carbon-intensive the ERM is and/or higher the net electricity export into the grid is. The results are discussed and put into perspective. Further research demands as well as product development opportunities are outlined. The importance of a green hydrogen economy is emphasized. 相似文献
997.
《International Journal of Hydrogen Energy》2019,44(8):4197-4207
Three CuO-ZnO-ZrO2-MxOy (CZZM, M = Cr, Mo and W) mixed oxides were prepared by a co-precipitation method and tested as catalysts for methanol synthesis from CO2 hydrogenation. The catalysts were characterized by XRD, N2 adsorption/desorption, XPS, reactive N2O adsorption, H2-TPR, and CO2-TPD techniques. The results indicated that the methanol selectivity and yield of the CuO-ZnO-ZrO2 catalyst noticeably increased by the additions of MoO3 and WO3, but slightly decreased by Cr2O3 doping. Combining with the characterization results, the difference in methanol yield over the three catalysts can be attributed to the differences in their BET specific surface areas (SBET) and adsorption capacities for CO2, while the methanol selectivity is closely correlated to the ratio of surface contents of Zn to Cu, as well as the fraction of strong basic sites in the total basic sites of the investigated catalysts. 相似文献
998.
《International Journal of Hydrogen Energy》2019,44(47):25505-25513
Optimization of pre-treatment conditions has been achieved for total sugar release from banana peel powder waste (BPPW) feedstock modelled through a three-level Box-Behnken design (BBD) of the response surface methodology (RSM). A series of various runs were executed at varied acid (H2SO4) concentrations (0.05%–0.15% v/v), incubation periods (1 h–3 h) in water bath at 95 °C and alkali (NaOH) concentrations (0.05%–0.15% v/v) according to the Box-Behnken design (BBD). From RSM the significant values of incubation period, acid concentration and alkali concentration were obtained as 3 h, 0.095% v/v, and 0.05% v/v respectively. The maximum total sugar release was reported as 5243.62 μg/ml which was highly close to the predicted value (5010.07 μg/ml). The model P- value (0.001), R-sq (98.26%), (adj) R-sq (95.14%) and (pred) R-sq (79.56%) obtained through ANOVA justified the results. The mutual impact of alkali and incubation period had the highest effect on total sugar release from dried banana peel powder, followed by mutual impact of acid and incubation period based on ANOVA (Analysis of Variance) results.Under optimized conditions of pre-treatment six different substrate concentrations (1%, 3%, 5%, 7% and 9% w/v) of BPPW was hydrolyzed and used to obtain volumetric bio-hydrogen evolution. The highest cumulative volumetric bio hydrogen gas 43 ml H2/30 ml media was achieved at 5% w/v of pretreated BPPW. The substrate concentration above 5% w/v resulted in lowered fermentation process owing to product and substrate inhibition. 相似文献
999.
《International Journal of Hydrogen Energy》2019,44(45):24342-24352
To achieve high activity and stability for both hydrogen and oxygen evolution reactions through the non-precious-metal based electrocatalysts is still facing the great challenge. Herein, we demonstrate a facile strategy to prepare CoP nanoparticles (NPs) loaded on N, P dual-doped carbon (NPC) electrocatalysts with high concentration N and P dopants through a pyrolysis-deposition-phosphidation process. The great bifunctional electrocatalytic activity for both HER (the overpotential of 98 mV and 86 mV at 10 mA cm−2 in both 0.5 M H2SO4 and 1 M KOH electrolytes, respectively) and OER (the overpotential of 300 mV at 10 mA cm−2 in 1 M KOH electrolyte) were achieved. When CoP@NPC hybrid was used as two electrodes in the 1 M KOH electrolyte system for overall water splitting, the needed cell potential for achieving the current density of 10 mA cm−2 is 1.6 V, and it also showed superior stability for HER and OER after 10 h’ test with almost negligible decay. Experimental results revealed that the P atoms in CoP were the active sites for HER and the CoP@NPC hybrid showed excellent bifunctional electrocatalytic properties due to the synergistic effects between the high catalytic activity of CoP NPs and NPC, in which the doping of N and P in carbon led to a stronger polarization between Co and P in CoP, promoting the charge transfer from Co to P in CoP, enhancing the catalytic activity of P sites and Co sites in CoP for HER and OER, respectively. Specifically, the improvements could result from the changed charge state, the increased active specific surface area, and the facilitated reaction kinetics by N, P co-doping and admixture. This work provides a high-efficient, low-cost and stable electrocatalyst for overall water splitting, and throws light on rational designing high performance electrocatalysts. 相似文献
1000.
《International Journal of Hydrogen Energy》2019,44(47):25652-25661
Surface decoration of photoanodes with oxygen evolution cocatalysts is an efficient approach to improve the photoelectrochemical water splitting performance. Herein, ultrafine CoOx was selectively immobilized on the surface of BiVO4/WO3 photoanode by using the photogenerated holes to in-situ oxidize Co4O4 cubane. The composited photoanode (CoOx/BiVO4/WO3) displayed an enhanced photoelectrochemical (PEC) water oxidation performance, with a photocurrent density of 2.3 mA/cm2 at 1.23 VRHE under the simulated sunlight irradiation, which was 2 times higher than that of bare BiVO4/WO3. The characterization results for the morphological, optical and electrochemical properties of the photoelectrodes revealed that, the enhanced PEC performances could be attributed to the improved charge carrier separation/transport behaviors and the promoted water oxidation kinetics when the photoelectrodes were loaded with CoOx. 相似文献