Enhancement of vertical phase separation in sequentially deposited organic photovoltaics through the independent processing of additives

Herein,the impact of the independent control of processing additives on vertical phase separation in sequentially deposited (SD) organic photovoltaics (OPVs) and its subsequent effects on charge carrier kinetics at the electron donor-acceptor interface are investigated.The film morphology exhibits notable variations,significantly depending on the layer to which 1,8-diiodooctane (DIO) was applied.Grazing incidence wide-angle X-ray scattering analysis reveals distinctly separated donor/acceptor phases and vertical crystallinity details in SD films.Time-of-flight secondary ion mass spectrometry analysis is employed to obtain component distributions in diverse vertical phase structures of SD films depending on additive control.In addition,nanosecond transient absorption spectroscopy shows that DIO control significantly affects the dynamics of separated charges in SD films.In SD OPVs,DIO appears to act through distinct mechanisms with minimal restriction,depending on the applied layer.This study emphasizes the significance of morphological optimization in improving device performance and underscores the importance of independent additive control in the advancement of OPV technology.

Solid Additive-Assisted Layer-by-Layer Processing for 19%Efficiency Binary Organic Solar Cells

Morphology is of great significance to the performance of organic solar cells(OSCs),since appropriate morphology could not only promote the exciton dissociation,but also reduce the charge recombination.In this work,we have developed a solid additive-assisted layer-by-layer(SAA-LBL)processing to fabricate high-efficiency OSCs.By adding the solid additive of fatty acid(FA)into polymer donor PM6 solution,controllable pre-phase separation forms between PM6 and FA.This intermixed morphology facilitates the diffusion of acceptor Y6 into the donor PM6 during the LBL processing,due to the good miscibility and fast-solvation of the FA with chloroform solution dripping.Interestingly,this results in the desired morphology with refined phase-separated domain and vertical phase-separation structure to better balance the charge transport/collection and exciton dissociation.Consequently,the binary single junction OSCs based on PM6:Y6 blend reach champion power conversion efficiency(PCE)of 18.16%with SAA-LBL processing,which can be generally applicable to diverse systems,e.g.,the PM6:L8-BO-based devices and thick-film devices.The efficacy of SAA-LBL is confirmed in binary OSCs based on PM6:L8-BO,where record PCEs of 19.02%and 16.44%are realized for devices with 100 and 250 nm active layers,respectively.The work provides a simple but effective way to control the morphology for high-efficiency OSCs and demonstrates the SAA-LBL processing a promising methodology for boosting the industrial manufacturing of OSCs.

Determining the Main Gas-generation Phase of Marine Organic Matters in Different Occurrence States using the Kinetic Method

This paper probes the determination of the main gas-generation phase of marine organic mattes using the kinetic method. The main gas-generation phase of marine organic matters was determined by coupling the gas generation yields and rates in geological history computed by the acquired kinetic parameters of typical marine organic matters （reservoir oil, residual bitumen, lowmaturity kerogen and residual kerogen） in both China and abroad and maturity by the EasyRo（%） method. Here, the main gas-generation phase was determined as Ro%=1.4%-2.4% for type Ⅰ kerogen, Ro%=1.5-3.0% for low-maturity type Ⅱ kerogen, Ro%=1.4-2.8% for residual kerogen, Ro%=1.5-3.2% for residual bitumen and Ro%=1.6-3.2% for reservoir oil cracking. The influences on the main gas-generation phase from the openness of the simulated system and the ＂dead line＂ of natural gas generation are also discussed. The results indicate that the openness of simulation system has a definite influence on computing the main gas-generation phase. The main gas-generation phase of type Ⅱ kerogen is Ro%=1.4-3.1% in an open system, which is earlier than that in a closed system. According to our results, the ＂dead line＂ of natural gas generation is determined as Ro=3.5 % for type Ⅰ kerogen, Ro=4.4-4.5% for type Ⅱ kerogen and Ro=4.6% for marine oil. Preliminary applications are presented taking the southwestern Tarim Basin as an example.

Mass Transfer Enhancement of Gas Absorption by Adding the Dispersed Organic Phases

由增加一个驱散的器官的阶段的煤气的吸收的集体转移改进在这个工作被学习了。各种各样的驱散的器官的阶段(heptanol， octanol， isoamyl 白酒， heptane，辛烷，和异辛烷) 在实验分别地被测试。根据理论模型和试验性的数据的意见，全面容量的集体转移系数和改进因素在不同驱散的器官的阶段卷部分和激动人心的速度下面被获得。试验性的结果显示煤气液体的集体转移被增加一个驱散的器官的阶段在不同水平提高。改进的最好的表演与驱散的器官的阶段被完成 5% 并且在 670 r 慭整楲污 ? 硥楨楢? 硥散汬湥 ?敭档湡捩污瀠潲数瑲敩 s

Organic acids and inorganic anions in Bayer liquors by ion chromatography after solid-phase extraction

A method for the simultaneous separation and determination of organic acids and inorganic anions in Bayer liquors was developed by gradient ion chromatography with suppressed conductivity detection. Formate, acetate, propionate, oxalate, succinate, glutarate, fluoride, chloride and sulfate were separated and determined in 33 min. The samples were pretreated with solid-phase extraction, which has high selectivity for removing a large number of metallic ions in the Bayer liquors, and filtered with a 0.45 μm filter membrane before being injected into the ion chromatographic system. The separation of six organic acids and three inorganic anions was achieved on an IonPac AS11-HC column with KOH as the eluent, and the detection was performed by a conductivity detection mode. No interference is found in the presence of fluorate, chlorate and sulphate when organic acids are determined. The calibration graphs of peak area for all the analytes are linear over a wide range. The relative standard derivation of the peak area of analytes is less than 2.14%. Under optimum conditions the detection ranges from 0.2 to 100.0 mg/L. The average recoveries of the added standards are between 94.3% and 102.8%.

Study of the Liquid Phase Volume Expansion for CO_2/Organic Solvent Systems

The supercritical antisolvent (SAS) process has been developed in recent years for the formation of nano- and micro-particles. It is necessary to study the liquid phase volume expansion (LPVE) and find the relationships between the operating conditions and the LPVE in order to develop a practical method for determining the operation conditions and selecting an organic solvent for SAS process. The PR equation of state with vdW-1 mixing rule is used to calculate the LPVE for CO2/toluene, CO2/acetone and CO2/ethyl acetate systems, and the results show that the LPVE for each CO2/organic solvent system decreases as the temperature increases. The relationship between the LPVE and the solubility of CO2 in the liquid phase for CO2/organic solvent systems is investigated, and the results show that the LPVE is determined directly by the solubility of CO2 in the liquid phase, xCO2, and can be related to xCO2 independently. No matter what system of CO2/organic solvent is and how different the temperature is, the LPVEs have little difference as long as the solubility of CO2 in the liquid phase, xCO2 > keeps constant. The lower temperature is always favorable to the SAS process. The higher the solubility of CO2 in an organic solvent under certain operation condition, the more suitable it is to the SAS process.

Analysis of the Law of Organic Solid Phase Precipitation and Deposition during Carbon Dioxide Displacement Process

Carbon Capture, Utilization and Storage (CCUS) has been regarded as an indispensable, strategic and pressing technology to reduce anthropogenic carbon dioxide emissions, and mitigate the severe consequences of climate change. Its utilization and storage play important roles in this system and they can be applied for oceanic and underground geological sequestration especially for the oil gas reservoir that needs to improve recovery. For the carbon dioxide flooding process, the crude oil displacement generally shows a better performance with the increase of the pressure. However, carbon disposal is always complex. It could encounter organic solid phase precipitation and deposition in near miscibility environment. The law of multiphase and multicomponent diversification in the whole processes is still poorly understood. We thus used the method of slim tube to get dynamic data during the process. Indeed, the interval of near minimum miscibility pressure was determined. Analysis results of injectivity index and productivity index show that the reservoir blockage primarily appears as the displacement pressure is higher than the near minimum miscibility lower limit pressure and plays an important role in the production capacity. Extortionate or low pressure is not conducive to carbon dioxide displacement.

Blocking Behavior of Organic Solid Phase in the Carbon Dioxide Multiphase and Multicomponent Displacement Process

Better dealing with carbon issues can support the management of current greenhouse gas emissions while achieving energy economic diversification and energy security. Carbon dioxide displacement has become the most acknowledged and practical method in enhanced oil recovery system. This is because of its oil sweep efficiency and ability to reduce the level of greenhouse gas emission. Nevertheless, it would lead to the organic solid phase deposition, which causes the changes of the wettability and the damages of wellbores and reservoirs. In this study, we used slim tube test and component test to research the dynamic characteristics of displacement process. In addition, the mechanism of porous media blockage was also investigated. Results show that when the displacement pressure closed to the minimum miscibility pressure, reservoir blockage in pore throat could happen. Component test characterizes that during near miscible displacement process, the components of oil sample varied obviously, the variation range of peak component carbon marks fluctuated strongly. Crude oil component differentiation could happen after carbon dioxide fully contacted with oil. Besides, the rapid extraction mechanism of aromatic hydrocarbons played a significant role in this process under such condition. The reason is that the solubility of saturated hydrocarbons to asphaltene and non-hydrocarbons is obviously weaker than aromatic hydrocarbons. Controlling the pressure is considered as an important link to prevent the occurrence of blocking in the carbon dioxide multiphase and multicomponent displacement process.

Liquid-phase synthesis of Li_(2)S and Li_(3)PS_(4) with lithium-based organic solutions

Sulfide solid electrolytes are widely regarded as one of the most promising technical routes to realize all-solid-state batteries(ASSBs)due to their high ionic conductivity and favorable deformability.However,the relatively high price of the crucial starting material,Li_(2)S,results in high costs of sulfide solid electrolytes,limiting their practical application in ASSBs.To solve this problem,we develop a new synthesis route of Li_(2)S via liquid-phase synthesis method,employing lithium and biphenyl in 1,2-dimethoxyethane(DME)ether solvent to form a lithium solution as the lithium precursor.Because of the comparatively strong reducibility of the lithium solution,its reaction with sulfur proceeds effectively even at room temperature.This new synthesis route of Li_(2)S starts with cheap precursors of lithium,sulfur,biphenyl and DME solvent,and the only remaining byproduct(DME solution of biphenyl)after the collection of Li_(2)S product can be recycled and reused.Besides,the reaction can proceed effectively at room temperature with mild condition,reducing energy cost to a great extent.The as-synthesized Li_(2)S owns uniform and extremely small particle size,proved to be feasible in synthesizing sulfide solid electrolytes(such as the solid-state synthesis of Li_(6)PS_(5)C_(l)).Spontaneously,this lithium solution can be directly employed in the synthesis of Li_(3)PS_(4) solid electrolytes via liquid-phase synthesis method,in which the centrifugation and heat treatment processes of Li_(2)S are not necessary,providing simplified production process.The as-synthesized Li_(3)PS_(4) exhibits typical Li+conductivity of 1.85×10^(-4) S·cm^(-1) at 30℃.

Growth of a-Plane GaN Films on r-Plane Sapphire by Combining Metal Organic Vapor Phase Epitaxy with the Hydride Vapor Phase Epitaxy

Hydride vapor phase epitaxy （HVPE） is utilized to grow nonpolar a-plane GaN layers on r-plane sapphire templates prepared by metal organic vapor phase epitaxy （MOVPE）. The surface morphology and microstructures of the samples are characterized by atomic force microscopy. The full width at half maximum （FWHM） of the HVPE sample shows a W-shape and that of the MOVPE sample shows an M-shape plane with the degree of 0 in the high-resolution x-ray diffraction （HRXRD） results. The surface morphology attributes to this significant anisotropic. HRXRD reveals that there is a significant reduction in the FWHM, both on-axis and off-axis for HVPE GaN are compared with the MOVPE template. The decrease of the FWHM of E2 （high） Raman scat tering spectra further indicates the improvement of crystal quality after HVPE. By comparing the results of secondary- ion-mass spectroscope and photoluminescence spectrum of the samples grown by HVPE and MOVPE, we propose that C-involved defects are originally responsible for the yellow luminescence.

APPLICATION OF THE SULFONATE ESTER GROUP AS A LINKER FOR SOLID PHASE ORGANIC SYNTHESIS

A use of Sulfonate ester as a linker in synthesis of (-aminoalkanols was reported. Diols were tethered onto polystyryl sulfonyl chloride resin, yielding sulfonate resins (2). After cleaved by diethyl amine, diisopropylamine and propylamine respectively, three (-aminoalkanols were obtained.

Conformation of Organic Chain in Phase Transition of Hybrid(C1_2H_(25)NH_3)_2MnCl_4

The structural change in phase transition of hybrid （Cl2H25NH3）2MnCl4 was investigated. The temperature and the structures of the phase transition is investigated by thermal gravimetry （TG） and differential scanning calorimetry （DSC）, infrared spectrum （IR） and X-ray diffraction （XRD）. The results suggest that the phase transition is reversible and the structural change arises from the conformation change of the organic chain. The interlayer distance increases when the hybrid transforms from low temperature phase to high temperature phase. This is explained by the diffusion of gauche-bond along the organic chains and they move away from each other when the phase transition occurs. Combining the experimental data with theoretical calculation, we propose that organic chain of the hybrid in high temperature phase is the conformation of gauche-bond alternating with trans bond （noted as GTG＇TGTG＇TGTG＇T）.

Two Organic Phase Suspension Polymerization for Novel Hypercrosslinked Resin Bead by Polycondensation of CMB

The suspension polymerization with two organic phases was adopted to prepare spherical hypercrosslinked resin by self-polycondensation of 4,4′-bis-(chloromethyl)-1,1′-biphenyl (CMB). The chemical structure, morphology and pore characteristics of the novel spherical resin were characterized with Fourier transform infrared spectroscopy (FTIR), micrograph and Brunauer-Emmett-Teller (BET). It is found that the suspension system and stirring speed impose a great influence upon the regularity and size distribution of hypercrosslinked beads. To prepare CMB resin beads with diameter of about 300 μm, the optimal condition is as follows: stirring speed 300 r·min-1 , and the volume ratio of the two organic phases (nitrobenzene/dimethyl silicon oil) 1︰5. After the self-polycondensation and succedent post-crosslinking of CMB monomer, the spherical adsorbent presents high special surface area (1190 m2 ·g-1 ) and abundant pore volume (0.714 cm 3 ·g-1 ), and could be potentially applied in the adsorption of various organic molecules and synthesis of porous ion exchanger.

Magnetic metal organic framework for pre-concentration of ampicillin from cow milk samples

The aim of this study is a present of a simple solvothermal synthesis approach to preparation of Cu-based magnetic metal organic framework(MMOF)and subsequently its application as sorbent for ultrasound assisted magnetic solid phase extraction(UAMSPE)of ampicillin(AMP)from cow milk samples prior to high performance liquid chromatography-Ultraviolet(HPLC-UV)determination.Characteristics of prepared MMOF were fully investigated by different techniques which showed the exclusive properties of proposed sorbent in terms of proper functionality,desirable magnetic property and also high specific surface area.Different influential factors on extraction recovery including sorbent dosage,ultrasonic time,washing solvent volume and eluent solvent volume were assessed using central composite design(CCD)based response surface methodology(RSM)as an operative and powerful optimization tool.This is the first report for determination of AMP using MMOF.The proposed method addressed some drawbacks of other methods and sorbents for determination of AMP.The presented method decreases the extraction time(4 min)and also enhances adsorption capacity(250 mg/g).Moreover,the magnetic property of presented sorbent(15 emu/g)accelerates the extraction process which does not need filtration,centrifuge and precipitation procedures.Under the optimized conditions,the proposed method is applicable for linear range of 1.0-5000.0 μg/L with detection limit of 0.29 μg/L,satisfactory recoveries(≥95.0%)and acceptable repeatability(RSD less than 4.0%).The present study indicates highly promising perspectives of MMOF for highly effective analysis of AMP in complicated matrices.

Studies of Heterogeneous Hydrothermal Stripping from Iron-loaded Naphthenic Acid-Alcohol-Kerosen

The technique of hydrothermal stripping from mixed aqueous-organic systems is a promising method for synthesizing oxide ceramic powders for high-performance applications. Some factors influencing heterogeneous hydrothermal stripping with water from iron-loaded organic phase of naphthenic acidisooctyl alcoholkerosene, such as initial concentrations of iron and naphthenic acid, concentration of Fe2O3 搒eed, temperature and time, were investigated. Based on the experimental results, the rate equation was established. Nano-ferric oxide powders were obtained by the technique of hydrothermal stripping from the iron-loaded organic phase. The results suggest that the heterogeneous hydrothermal stripping proceeds in 3 steps: adsorption of naphthenic acid dimers and naphthenic complex of iron onto the surface of seed? hydrolysis of adsorbed complex of iron, and condensation of hydrolyzed complex. The process activation energy is 115 kJ/mol and the heterogeneous hydrothermal stripping is controlled by a chemical reaction (the hydrolysis of naphthenic complex of iron).

Amperometric Biosensors Sensitive to Organic Peroxides Based on Immobilization of Redox Organic Dyes and Horseradish Peroxidase in Polyester Ionomer Film

Simple and effective organic biosensors sensitive to organic peroxides such as 2 butanone per oxide and tertbutyl hydroperoxide are constructed by immobilizing a series of redox organic dyes and horseradish peroxidase in Eastman AQ polymer film. The organic dyes are methylene blue, methylene green, meldola blue, new methylene blue N and N methyl phenazine methosulphate. The biosensors display high sensitivity and fast response to tertbutyl hydroperoxide and 2 butanone peroxide because of high efficiency of electron transfer between immobilized horseradish peroxidase and the electrode via the redox organic dyes. The comparison of the biosensors employing different organic dyes is made in formal potential, linear range and response time.

Ferrimagnetism and metal insulator transition in an organic polymer chain

The ferrimagnetism and quantum phase transition of a bipartite lozenge periodic Anderson-like organic polymer, in which the localized f electrons hybridize with the odd site conduction orbitals, are investigated by means of Green＇s function theory. The ground state turns out to be gapless ferrimagnetism. At a finite temperature, the ferrimagnetic-to- paramagnetic phase transition takes place. The Kondo screenings and Ruderman-Kittel-Kasuya-Yosida （RKKY） inter- action can reduce and increase the transition temperature, respectively. Two Kondo screenings compete with each other, giving rise to the localized f electron spin screened antiferromagnetically. Accordingly, in a magnetic field, all spins are aligned along the chain easily, which is associated with metal-insulator transition. Furthermore, in a temperature-field plane, we reveal the gapless and spin polarized phases, which are characterized by susceptibility and specific heat, and whose behaviours are determined by the competition between the up-spin and down-spin hole excitations.

Novel additives for the separation of organic acids by ion-pair chromatography

This paper proposes the use of novel surfactant additives for the separation of organic acids by ion-pair chromatography and studies the influences of surfactants on the chromatographic separation behaviors.Researches have been carried out on both silica gel matrix and polymer supporters in order to compare the two ordinary kinds of stationary phases,and the phenomenon is similar. Separation is based on differences in the stabilities of analyte-additive complexes in solution.Retention times of analytes can ...