- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Selective recovery of indium via continuous counter-current foam separation from sulfuric acid solutions I – Application of anionic organophosphate surfactant as metal collector
摘要： Continuous counter-current foam separation (CCFS) with simultaneous injections of metal and surfactant solutions respectively into rising foam bed was applied to In(III) recovery from sulfuric acid solutions containing ternary metal ions of In/Cu/Zn. Through the screening tests of the surfactants in both conventional batch foam separation and CCFS, anionic organophosphate surfactant which has similar structure to phosphoric acid extractant (D2EHPA) was selected as the metal collector, with an addition of a nonionic co-surfactant as the foam stabilizer. The optimized surfactant combination was shown anionic A219B/nonionic POOE20 in this study; the complete recovery of In(III) was attained with the enrichment ratio of 5.5, whereas those of the other metals were suppressed in trace level, resulting in the excellent selective recovery. Moreover, metal solutions of quaternary In/Fe/Cu/Zn were also examined, and a dose of reductant for interfering Fe(III) into the metal solution was executed for improving the separation efficiency; the dose of ascorbic acid could invert the affinity order of A219B from Fe > In to In > Fe. The percent recovery and enrichment ratio of In(III) were 97% and 5.5, while the separation factors of In/Fe, In/Cu and In/Zn were 93, 1300 and 1300 respectively. This is our first favorable case for expanding the choice range of target metal ions in CCFS using anionic surfactants.
关键词： Foam fractionation,Indium recovery,Anionic organophosphate surfactant,Phosphorus acid extractant,Foam separation
更新于2025-09-23 15:22:29
-
Surfactant-free stable SnS2 nanoparticles dispersion for deposition of device-quality films
摘要： Tin sulfide (SnS2) has recently attracted considerable attention due to its layered structure that may form two dimensional morphologies. It is an n-type semiconductor with band gap and electron affinity similar to CdS and In2S3; therefore can be regarded as an alternative for these materials in thin film solar cells. Here, we synthesis of SnS2 nanoparticles with different morphology in different ratio of water-ethanol mixed solution by solvothermal method, and observe that more ethanol leads to large sheet like morphologies, while water based synthesis results in very small nanosheets. A challenge in wet deposition of device-quality thin films of SnS2 is the requirement for highly dispersed particles/sheets. We found highly polar dimethylformamide (DMF) as the right dispersing medium, yielding highly stable dispersions. Very uniform nanocrystalline thin films with [001] preferred orientation and good adhesion to substrate are simply deposited by drop casting and spin coating a 0.5 wt% DMF sol of SnS2 at 2000 rpm for 1 min. Electron affinity and band gap of the films are 4.33 eV and 2.27 eV, which is well aligned for copper indium gallium sulfo-selenide (CIGS) solar cells.
关键词： Two dimensional structures,Surfactant-free dispersion,copper indium gallium sulfo-selenide solar cells,SnS2 thin film,Dimethylformamide,Buffer layer
更新于2025-09-23 15:21:21
-
Investigating the Photovoltaic Performance of Surfactant assisted MoBi2Se5 Thin Films
摘要： MoBi2Se5 has been proved to be a promising material for the photoelectrochemical solar cell application. As, MoBi2Se5 thin films are more corrosion resistant than Bi2Se3 thin films also MoBi2Se5 can be used as a buffer layer due to its distinctive optostructural properties. In this study, we have synthesized surfactant assisted nanostructured MoBi2Se5 thin films by using cost effective chemical route, i.e. arrested precipitation technique (APT). The synthesized thin films were analyzed for their Opto-structural, surface morphological, compositional and photovoltaic application using X-ray diffraction Technique (XRD), UV-Vis Spectroscopy, Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDAX) and its photoelectrochemical solar cell performance was checked respectively. The nanocrystalline nature of MoBi2Se5 thin films was confirmed from the XRD pattern. An increment in the optical band gap energy was observed with surfactant mediation. The surface morphology of MoBi2Se5 was changed from spherical to spongy balls like nanofibrous surface morphology after surfactant assistant. Furthermore, both the as synthesized and surfactant assisted MoBi2Se5 thin films showed the photoelectrochemical solar cell applicability.
关键词： thin films,arrested precipitation technique,MoBi2Se5,surfactant,photoelectrochemical solar cell
更新于2025-09-23 15:21:01
-
A novel CdTe ink-assisted direct synthesis of CdTe thin films for the solution-processed CdTe solar cells
摘要： The CdTe ink in thiol-amine cosolvents from CdTe powder has been successfully prepared via Triton X-100 surfactant at 50 °C. The CdTe thin films have been synthesized and characterized from the prepared CdTe ink using spin coating method. The SEM micrographs reveal that synthesized films are uniform, smooth and homogeneous with less cracks, voids and pinholes compared to the films deposited from the inks without surfactant. The XRD spectra confirm the mixed hexagonal and cubic structure of the deposited films. The Raman peaks at 142 and 122 cm-1 indicate the CdTe and the pure Te phase, respectively. The FTIR peaks at 1638 and 1384 cm-1 due to C=O and COO- groups originated for the stretching vibration of the ligands of the thiol-capped CdTe, and the absence of vibrational peaks of S–H in the range of 2550–2650 cm-1 confirms the thiol-capped CdTe, respectively. The EDX results reveal the existence of Cd and Te elements in CdTe films. The deposited films exhibit the highest absorbance (*85%) with a band gap of 1.5 eV. Hall studies and electrical analysis indicate the high quality of the CdTe films. Therefore, it can be concluded that the developed surfactant-mediated CdTe ink is highly promising for solution-processed CdTe-based photovoltaics.
关键词： spin coating,Triton X-100 surfactant,thiol-amine cosolvents,CdTe ink,CdTe thin films,photovoltaics
更新于2025-09-23 15:21:01
-
Role of Morphology of Surfactant-Free Nanoparticles in Organic Photovoltaics
摘要： Nanoparticulate (NP) ?lms and organic photovoltaic devices have been fabricated from poly(3-hexylthiophene):phenyl C61 butyric acid methyl ester (P3HT:PC61BM) NP aqueous dispersions prepared by the precipitation method. The NP inks were stable for more than 4 days, and nanoparticle organic photovoltaic (NP-OPV) devices with ef?ciency (g) of 1% were fabricated. Detailed analysis of the morphology and performance of the precipitated NP-OPV devices indicated that an optimal blend is responsible for the photocurrent and ef?ciency observed. These results were con?rmed by grazing-incidence x-ray diffraction (GIXRD) analysis, which revealed that the precipitated NPs were resistant to thermal phase segregation, allowing thermal conditioning of the NP ?lms. These results show that precipitated NPs provide a pathway to thermally stable NP-OPV devices with higher photocurrents and ef?ciencies, approaching those of optimal bulk heterojunction (BHJ) OPV devices.
关键词： ink stability,Organic photovoltaic cells (OPV),nanoparticle (NP),nanoparticle morphology,precipitation,surfactant-free
更新于2025-09-23 15:21:01
-
siRNA Delivery Using Dithiocarbamate-Anchored Oligonucleotides on Gold Nanorods
摘要： We present a robust method for loading small interfering RNA (siRNA) duplexes onto the surfaces of gold nanorods (GNRs) at high density, using near-infrared (NIR) laser irradiation to trigger their intracellular release with subsequent knockdown activity. Citrate-stabilized GNRs were first coated with oleylsulfobetaine (OSB), a zwitterionic amphiphile with low cytotoxicity, which produced stable dispersions at high ionic strength. Amine-modified siRNA duplexes were converted into dithiocarbamate (DTC) ligands and adsorbed onto GNR surfaces in a single incubation step at 0.5 M NaCl, simplifying the charge screening process. The DTC anchors were effective at minimizing premature siRNA desorption and release, a common but often overlooked problem in the use of gold nanoparticles as oligonucleotide carriers. The activity of GNR?siRNA complexes was evaluated systematically against an eGFP-producing ovarian cancer cell line (SKOV-3) using folate receptor-mediated uptake. Efficient knockdown was achieved by using a femtosecond-pulsed laser source to release DTC-anchored siRNA, with essentially no contributions from spontaneous (dark) RNA desorption. GNRs coated with thiol-anchored siRNA duplexes were less effective, and also permitted low levels of knockdown activity without photothermal activation. Optimized siRNA delivery conditions were applied toward the targeted knockdown of transglutaminase 2 (TG2), whose expression is associated with the progression of recurrent ovarian cancer, with a reduction in activity of over 80% achieved after a single pulsed laser treatment.
关键词： dithiocarbamates,siRNA,gold nanorods,zwitterionic surfactant,photothermal
更新于2025-09-23 15:21:01
-
Insights into mechanism of size-controlled synthesis of CH3NH3PbBr3 perovskite quantum dots and large nanoparticles with tunable optical properties
摘要： There is a common phenomenon in the preparation of perovskite quantum dots (QDs) by reprecipitation method that large particles were always produced with desired QDs. Understanding the fabrication mechanism can contribute to improve this phenomenon. Herein, we demonstrate a two-step strategy for synthesis of perovskite QDs and large nanoparticles (LNPs), where the growth of QDs and LNPs involves two possible pathways, the quick intercalation reaction process and the dissolution-recrystallization process. Following two pathways, we have created QDs with high photoluminescence quantum yields (ca. 46–71%), tunable size (ca. 3.2–5.4 nm) and LNPs with tunable size from 25 to 300 nm, where their emission wavelength can be tuned from 500 nm to 534 nm. Importantly, based on the comprehensive insight into the formation mechanism, we have achieved the conversion from LNPs to QDs partly through adding surfactants properly, which is expected to pave the way for the development of pure production of perovskite QDs.
关键词： Surfactant ligands,Quantum dots,Optical properties,Hybrid organic-inorganic perovskite,Size-controlled
更新于2025-09-23 15:21:01
-
Ultrathin two-dimensional conjugated metala??organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
摘要： Two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have recently emerged for potential applications in (opto-)electronics, chemiresistive sensing, and energy storage and conversion, due to their excellent electrical conductivity, abundant active sites, and intrinsic porous structures. However, developing ultrathin 2D c-MOF nanosheets (NSs) for facile solution-processing and integration into devices remains a great challenge, mostly due to unscalable synthesis, low yield, limited lateral size and low crystallinity. Here, we report a surfactant-assisted solution synthesis toward ultrathin 2D c-MOF NSs, including HHB-Cu (HHB=hexahydroxybenzene), HHB-Ni and HHTP-Cu (HHTP=2,3,6,7,10,11-hexahydroxytriphenylene). For the first time, we achieve single-crystalline HHB-Cu(Ni) NSs featured with a thickness of 4-5 nm (~8-10 layers) and a lateral size of 0.25-0.65 μm2, as well as single-crystalline HHTP-Cu NSs with a thickness of ~5.1±2.6 nm (~10 layers) and a lateral size of 0.002-0.02 μm2. Benefiting from the ultrathin feature, the synthetic NSs allow fast ion diffusion and high utilization of active sites. As a proof of concept, when serving as a cathode material for Li-ion storage, HHB-Cu NSs deliver a remarkable rate capability (charge within 3 min) and long-term cycling stability (90% capacity retention after 1000 cycles), superior to the corresponding bulk materials and other reported MOF cathodes.
关键词： Li-ion batteries,Two-dimensional conjugated metal-organic frameworks,electrochemical performance,surfactant-assisted synthesis,ultrathin nanosheets
更新于2025-09-23 15:19:57
-
Formation of Size and Density Controlled Nanostructures by Galvanic Displacement
摘要： Gold (Au) and copper (Cu)-based nanostructures are of great interest due to their applicability in various areas including catalysis, sensing and optoelectronics. Nanostructures synthesized by the galvanic displacement method often lead to non-uniform density and poor size distribution. Here, density and size-controlled synthesis of Au and Cu-based nanostructures was made possible by galvanic displacement with limited exposure to hydrofluoric (HF) acid and the use of surfactants like L-cysteine (L-Cys) and cetyltrimethylammonium bromide (CTAB). An approach involving cyclic exposure to HF acid regulated the nanostructure density. Further, the use of surfactants generated monodisperse nanoparticles in the initial stages of the deposition with increased density. The characterization of Au and Cu-based nanostructures was performed by scanning electron microscopy, atomic force microscopy, UV-Visible spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy and X-ray diffraction. The surface enhanced Raman spectroscopic measurements demonstrated an increase in the Raman intensity by two to three orders of magnitude for analyte molecules like Rhodamine 6G dye and paraoxon.
关键词： monodisperse,sensing,surfactant,nanostructures,gold
更新于2025-09-23 15:19:57
-
High-throughput Proteomics Enabled by a Photocleavable Surfactant
摘要： Mass spectrometry (MS)-based proteomics provides unprecedented opportunities for understanding the structure and function of proteins in complex biological systems; however, protein solubility and sample preparation before MS analysis remain a bottleneck preventing high-throughput proteomics. Herein, we report for the first time a high-throughput bottom-up proteomics method enabled by a newly developed MS-compatible photocleavable surfactant, 4-hexylphenylazosulfonate (Azo)[1] that facilitates robust protein extraction, rapid enzymatic digestion (30 min compared to overnight), and subsequent MS-analysis following UV degradation. Moreover, we developed an Azo-aided bottom-up method for efficient analysis of integral membrane proteins, which are key drug targets and are generally underrepresented in global proteomic studies. Furthermore, we demonstrated the unique ability of Azo to serve as an “all-in-one” MS-compatible surfactant for both top-down and bottom-up proteomics, with streamlined workflows for high-throughput proteomics amenable to clinical applications.
关键词： membrane proteomics,high-throughput proteomics,photocleavable surfactant
更新于2025-09-23 15:19:57