Ultrathin perovskite based solar cells with the efficiency enhanced by charge transfer process

We report a new approach of improving the solar cells efficiency based on ultrathin perovskite films. We propose the addition of CuPc compound to perovskite active layer for enhanced charge generation and transfer process by charge transfer process between CuPc and perovskite. The performance of the devices with and without addition of CuPc was studied in respect to thickness of the active layer. The thickness was varied by the change of the spin coating speed in the range of 4000, 7000 and 10000 rpm, different concentration of CuPc also been studied. The process of charge carrier recombination, crystallinity and Raman characteristics of the obtained films was studied. The perovskite device with an active layer of MAPbI₃ mixed with CuPc spin coated with the speed of 10000 rpm with thickness of about 150 nm demonstrated the efficiency of 12.7%. The ultrathin mixed perovskite film (10000 rpm perovskite film of 15% CuPc) based device presents 33% thickness and 85% efficiency of common pure perovskite device (4000 rpm pure perovskite film).     

Chemical Bonding by the Chemical Orthogonal Space of Reactivity

The fashionable Parr–Pearson (PP) atoms-in-molecule/bonding (AIM/AIB) approach for determining the exchanged charge necessary for acquiring an equalized electronegativity within a chemical bond is refined and generalized here by introducing the concepts of chemical power within the chemical orthogonal space (COS) in terms of electronegativity and chemical hardness. Electronegativity and chemical hardness are conceptually orthogonal, since there are opposite tendencies in bonding, i.e., reactivity vs. stability or the HOMO-LUMO middy level vs. the HOMO-LUMO interval (gap). Thus, atoms-in-molecule/bond electronegativity and chemical hardness are provided for in orthogonal space (COS), along with a generalized analytical expression of the exchanged electrons in bonding. Moreover, the present formalism surpasses the earlier Parr–Pearson limitation to the context of hetero-bonding molecules so as to also include the important case of covalent homo-bonding. The connections of the present COS analysis with PP formalism is analytically revealed, while a numerical illustration regarding the patterning and fragmentation of chemical benchmarking bondings is also presented and fundamental open questions are critically discussed.     

基于区间犹豫模糊语言集的水资源多目标决策

以鄂北水资源配置工程为对象,研究大型调水工程背景下的多水源多目标优化配置。将鄂北地区水库分为充蓄水库、补偿水库与在线水库等3类,根据各类水库特点对鄂北水资源配置工程进行系统概化,建立以年缺水量最小和调水成本最低为目标函数的多水源多目标优化配置模型。采用权重系数法进行求解得到非劣解集。最后采用基于区间犹豫模糊语言与TOPSIS的多目标决策方法对各方案的缺水量与调水量作出评价并遴选出最优方案。研究结果表明:对鄂北水资源配置工程而言,缺水量与调水量的权重比为7∶3的方案综合评价最优,重视缺水的同时兼顾调水成本;基于区间犹豫模糊语言集与TOPSIS的水资源多目标决策方法经本文实例验证具有较高的稳定性与可行性。     

Effects of external light load on posture and foot pressure distribution in young adults: A pilot study

Holding an asymmetrical load, like a rucksack, grocery bag, or travel backpack, is a part of daily and occupational activities. This pilot study was aimed to determine the effects of light, asymmetrical, handheld load on the body posture and foot pressure distribution in young adults. Thirteen young volunteers, free of any injury or pain, took part in the study (aged 21.53 ± 1.10 years). All the study participants were right-handed. An additional load (4 kg, placed in the rucksack) was asymmetrically held in each hand while standing still. For evaluation of the posture and foot pressure distribution, the investigation focused on three positions, i.e., no-load, a rucksack in the right hand, a rucksack in the left hand. We used a surface topography system and force platform for evaluation of the body posture and foot pressure examination, respectively. The results showed that the main changes in the body posture caused by an external load application manifested in trunk imbalance. The trunk was shifted in the direction opposite to the load. Trunk imbalance changes were statistically significant in all three comparisons (p = 0.001). Interestingly, changes in the rotations and lateral deviation seem to be dependent on the hand dominance. Greater foot pressure was observed on the loaded limb (p < 0.01), and highly significant differences were noted between the left and right foot in both loaded postures (p < 0.001). Further research needs to be done to check if lateralization is connected with body posture while holding an external load.     

Achieving High Electroluminescence Efficiency and High Color Rendering Index for All-Fluorescent White OLEDs Based on an Out-of-Phase Sensitizing System

Sensitizing conventional fluorescence (CF) dopants with thermally activated delayed fluorescence (TADF) materials has achieved considerable progress, by which the advantages of TADF materials and CF dopants can be fully harnessed. However, the usually used co-phase configuration of CF dopant-engaged sensitizing systems often encounters exciton loss due to Dexter energy transfer (DET). Herein, an effective out-of-phase configuration is proposed to sensitize CF dopants in the fabrication of white organic light-emitting diodes (WOLEDs). Based on a new efficient sky-blue TADF luminogen DCP-BP-DPAC which has an electroluminescence (EL) peak at 486 nm and an EL efficiency of 26.6%, a green TADF material BDMAC-XT, and a red CF dopant DBP sensitized by BDMAC-XT through an out-of-phase configuration without interlayer, efficient WOLEDs are successfully fabricated. By further adopting orange TBRB or 4CzTPNBu as intermediate sensitizers, more efficient energy transfer to DBP is achieved via Förster energy transfer. Through step-by-step energy transfer and elimination of excess DET process, high-performance all-fluorescent WOLEDs are achieved, providing excellent EL efficiencies over 23.0%, and highly stable white light with a high color rendering index of 87. The outstanding EL performance and high-quality emission color demonstrate the great potential of the proposed out-of-phase design for sensitizing systems of WOLEDs.     

Liquid Phase CO2-Analytics for Standardized Mass Transfer Characterization in Packed Columns

Mass transfer parameters are necessary for the design of absorption and desorption processes in packed columns. To determine the effective interfacial area and liquid side mass transfer parameters, CO₂ absorption and desorption are frequently used. Reliable analytics for concentration determination are essential to obtain correct results. In this work two methods of CO₂ liquid phase analysis are compared: first, the back titration of unreacted NaOH after prior precipitation of the bound CO₂; secondly, the inorganic carbon analysis with a commercial inorganic carbon analyzer.     

基于跨临界CO2热泵的茶叶生产能源系统负荷削减潜力

乡村产业中的化石能源设备逐渐被电能技术替代，引起了乡村负荷波动增大、部分时段产生集中高负荷的问题。为了解决以上问题，将低品位清洁能源应用至乡村的茶叶生产中，针对烘茶全过程的工艺要求提出了跨临界CO₂热泵烘茶技术；并以某茶叶生产乡村为对象，对其代表台区的全年日用电量及产茶日负荷进行了分析，得出采用CO₂热泵烘茶后其负荷得到大幅度削减，整体可降低至原负荷的39.6%~46.8%，峰值负荷与平时负荷的比值由原本的13.6降至5.4~6.2。跨临界CO₂热泵应用至农产品生产中可有效缓解乡村供电压力。     

A generalized CFD model for evaluating catalytic separation process in structured porous materials

A hybrid multiphase model is developed to simulate the simultaneous momentum, heat and mass transfer and heterogeneous catalyzed reaction in structured catalytic porous materials. The approach relies on the combination of the volume of fluid (VOF) and Eulerian–Eulerian models, and several plug-in field functions. The VOF method is used to capture the gas–liquid interface motion, and the Eulerian–Eulerian framework solves the temperature and chemical species concentration equations for each phase. The self-defined field functions utilize a single-domain approach to overcome convergence difficulty when applying the hybrid multiphase for a multi-domain problem. The method is then applied to investigate selective removal of specific species in multicomponent reactive evaporation process. The results show that the coupling of catalytic reaction and interface species mass transfer at the phase interface is conditional, and the coupling of catalytic reaction and momentum transfer across fluid–porous interface significantly affects the conversion rate of reactants. Based on the numerical results, a strategy is proposed for matching solid catalyst with operating condition in catalytic distillation application.     

Indirect charge transfer of holes via surface states in ZnO nanowires for photoelectrocatalytic applications

In this work, ZnO nanowires with high aspect ratio were obtained by fast and simple electrochemical anodization. Morphological, structural and photoelectrochemical characteristics of the synthesized ZnO nanowires were evaluated by using different techniques: field emission scanning electron microscopy, atomic force microscopy, high resolution transmission electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, UV–VIS spectroscopy, Mott-Schottky analysis and photoelectrochemical impedance spectroscopy. The synthesized ZnO nanowires presented high roughness and high crystallinity. Besides, surface defects were identified in the sample. The value of the donor density (N_D) was in the order of 10¹⁹ cm^?3 in the dark and 10²⁰ cm^?3 under illumination. In addition, the ZnO nanowires presented good photosensibility, with a photocurrent density response 85 times higher than a ZnO compact layer, and lower resistance to charge transfer. The charge transfer processes taking place at the ZnO/electrolyte interface were studied, since these processes strongly influence the photoelectrocatalytic efficiency of the material. According to the results, the charge transfer of holes in the synthesized ZnO nanowires occurs indirectly via surface states. In this regard, surface states may be an important feature for photoelectrocatalytic applications since they could provide lower onset voltages and higher anodic current densities.