Ink Stability Research Articles

Key Control Characteristics of Carbon Black Materials for Fuel Cells and Batteries for a Standardized Characterization of Surface Properties

AbstractCarbon Blacks (CBs) are primarily used in electrocatalysis as support materials for nanoparticulate electrocatalysts. In fuel cells, CBs, catalysts, and proton conductive polymers (ionomers) undergo a dispersion/homogenization process for electrode coating. The interactions between components in dispersion and the surface of CB particles are complex. The surface characteristics of CB particles impact slurry formulation, electrode coating, and the resulting electrode layer, affecting fuel cell and battery performance and durability. This study investigates commercially available CBs such as Vulcan XC72R, Ketjen Black EC‐300J, Ketjen Black EC‐600JD, and Super C65, focusing on application‐relevant key control characteristics (KCCs). The KCCs include physicochemical features like electrical conductivity (electron transport through the catalyst layer, CL), oxygen‐containing surface groups (hydrophilicity/phobicity of the CL, catalyst functionalization), surface basicity/acidity, ionomer adsorption, and particle dispersibility (catalyst ink stability). KCCs are determined by particle bulk electrical conductivity, Boehm titration (BT), isoelectric point (IEP), and Hansen solubility parameters (HSP). HSP, understood as similarity parameters for particles, indicate how nanoparticle surfaces interact with liquids during dispersion. The proposed KCCs serve as a starting point for characterizing CBs and guiding product design to obtain meaningful structure‐property relationships, essential for a successful energy transition.

Preparation of thermochromic ink from anthocyanidin-encapsulated alginate nanoparticles for anticounterfeiting applications.

In order to make commercial products less vulnerable to counterfeiting, thermochromic inks have proven to be a viable authentication strategy. Herein, we developed a thermochromic ink for authentication by combining an anthocyanidin (ACYD) extract with alginate (ALG). To increase the anthocyanidin/alginate ink stability, a mordant (ferrous sulfate) was employed to tie up the anthocyanidin biomolecules with alginate. ACYD was extracted from red-cabbage and then immobilized into alginate to serve as an environmentally friendly spectroscopic probe. Thermochromic composite inks (ACYD@ALG) were made by adjusting the content of anthocyanidin. A homogenous blue film (608 nm) was printed on a paper surface and investigated by the CIE Lab coordinate system. The blue color transformed into reddish (477 nm) when heated from 35°C to 65°C. Nanoparticles (NPs) of anthocyanidin/mordant (ACYD/M) were examined for their size and morphology to indicate diameters of 80-90 nm, whereas the ACYD/M-encapsulated alginate nanoparticles showed diameters of 120-150 nm. Multiple analytical techniques were utilized to examine the printed papers. The mechanical and rheological performance of both stamped sheets and ink fluid were explored. The cytotoxicity and antimicrobial efficacy of ink (ACYD@ALG) were investigated.

Enhancing proton exchange membrane water electrolysis performance: Impact of iridium oxide catalyst ink dispersing methodology

Iridium oxide (IrO2) is the most successful catalyst for triggering oxygen revolution reactions in proton exchange membrane water electrolyzers (PEMWE). However, conventional ultrasonic methods for ink dispersion often result in ink instability, catalyst aggregation, and sedimentation. To address these issues, we investigate the effects of the dispersion type, treatment time, and ionomer-addition sequence on the catalytic performance. Ball-milling procedure prepares a more stable catalyst ink and achieves a larger electrochemical surface area (ECSA) than ultrasonic method. Extending the ball-milling time to 12 h improves the ink stability (absorbance change rate ∼0.6 % h−1); however, over-processing causes the thickest catalyst layer, leading to an enhanced mass transport resistance. Moreover, treating an ionomer with IrO2 causes the substitution of sulfonic acid groups by carboxylic acid groups and reduces the repulsive force in colloidal particles, resulting in poor ink stability, low proton conductivity, and small ECSA. Therefore, adding ionomer after ball milling is recommended for the preparation of a stable ink with high catalytic performance. The membrane electrode assembly prepared using this procedure exhibits an improved performance of 1.70 A cm−2 at 1.7 V, compared with that prepared using ultrasonic methods. This work provides crucial guidance of ink preparation for large-scale production of PEMWEs.

3D printing of hybrid solid–liquid structures

Abstract3D printing is a versatile technology for creating objects with custom geometries and compositions and is increasingly employed for fabricating hybrid solid–liquid composites (SLCs). These composites, comprising solid matrices with integrated liquid components, showcase unique properties such as enhanced flexibility and improved thermal and electrical conductivities. This review focuses on methods to fabricate SLCs directly by different 3D printing techniques, e.g. without needing to backfill or impregnate a porous matrix. The techniques of extrusion, vat photopolymerization and material jetting combined with microfluidics, inkjet printing, vacuum filling and ultraviolet light curing to produce SLCs are emphasized. We also discuss the development of feedstocks, focusing on emulsions and polymer capsules as fillers, and analyze current literature to highlight their significance. The review culminates in a perspective on new directions, highlighting the potential of bicontinuous interfacially jammed emulsion gels (bijels) to facilitate the printing of continuous liquid pathways, alongside the importance of understanding ink formulation and stability. Concluding with future perspectives, we underline the transformative impact of 3D‐printed SLCs in diverse applications, signaling a significant advancement in the field. © 2024 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Industrial Chemistry.

Active mixing of two-component viscoelastic silicone ink at molecular level for spatiotemporally controlled 3D/4D printing of cellular silicones

3D printed silicones have demonstrated great potential in diverse areas such as soft robots, tissue engineering, flexible sensors and energy dissipation. However, most silicone inks face inevitable curing issue once it is prepared. During the materials extrusion based printing process, the curing-related viscosity change in silicone inks hamper the ink stability and printing controllability, leading to complex relationship among ink properties and printing parameters, as well as printing structures and material properties of final products. Herein, this work presents active mixing of two component silicone ink to realize stable printing, achieving exact and continuous match of ink properties and printing parameters. Using a specially formulated ink containing separate starting components with reactive groups, catalyst and thixotropic agents, this work studies the active mixing process thoroughly for the first time from molecular level to materials performances under various conditions regarding inlet flow rates, impeller rotation speed and component ratios. Besides, cellular silicones with controlled distribution of component ratios and tailored gradient structures are printed, leading to integrated manufacturing of compression performance and shape morphing property. This work will pave way for active mixing and printing of two-component silicones, and provide guidance for other reactive multi-material 3D printing systems.

Investigation of the 3D printability of modified starch-based inks and their formation mechanism: Application in ice cream

Traditional ice cream has not been amenable to 3D printing for personalized processing. Hence, this study chose modified starch to enhance the feasibility of 3D printing for ice cream. We selected 7 inks from the ice cream with 13 types of modified starch based on ink stability and rheological properties to investigate the forming mechanism of 3D-printed ice cream. The ice cream ink prepared with hydroxypropyl distarch phosphate (HDSP) exhibited the highest precision (94.6%), which was attributed to the presence of more hydrogen bonding support and stable protein structure in the ink. These intermolecular interactions resulted in excellent water retention and the formation of a dense gel structure, which further enhanced the elasticity, structure recovery rate (99.66%), and mechanical properties (1896.35Pa) of ink. These enhanced properties contributed to the extrusion of finer line widths (0.95 mm) in the 3D printing process and improved the self-supporting capabilities of printed products, thereby enhancing the accuracy of 3D printed ice cream. Further analysis of the texture properties of printed products provided a comprehensive evaluation of the application potential of modified starch in 3D-printed ice cream. This study offers novel insights into the use of starch materials for personalized production of ice cream.

Agglomeration behavior of carbon-supported platinum nanoparticles in catalyst ink: modeling and experimental investigation

Within catalyst inks, the agglomeration of carbon-supported Pt nanoparticles (Pt/C NPs) stands out as a primary destabilizing factor. This study simulates the agglomeration process of particles under varying ionic strengths (ISs), employing the Brownian motion of Pt/C NPs and inter-particle forces. The energy barriers (EBs) within particles govern particle interactions, subsequently translating into the adhesive efficiency of particle collisions (α). By modulating the ISs in Ink-P (IS = 0.00182), Ink-01 (IS = 0.01), and Ink-001 (IS = 0.001), the Zeta potential and EBs are diminished, thereby increasing α. Structural parameters of agglomerates during the agglomeration process, such as fractal dimension (df) and porosity, are computationally assessed using Matlab. The simulated df for Ink-P, Ink-001, and Ink-01 are 1.82, 1.62, and 1.54, respectively, while the experimentally measured df are 1.92–1.95, 1.67–1.7, and 1.56–1.59, confirming the effectiveness of the simulation method. High α led to isotropic growth of agglomerates, resulting in higher df. Increased IS causes compression of the electric double layer and higher α, ultimately leading to rapid destabilization of the ink. This method not only enhances comprehension of nanoscale particle agglomeration, explaining variations in ink stability and agglomerate structures, but also broadens its applicability to diverse nanoparticle dispersion systems.

Volatile Perovskite Precursor Ink Enables Window Printing of Phase-Pure FAPbI3 Perovskite Solar Cells and Modules in Ambient Atmosphere.

Despite the great success of perovskite photovoltaics in terms of device efficiency and stability using laboratory-scale spin-coating methods, the demand for high-throughput and cost-effective solutions remains unresolved and rarely reported because of the complicated nature of perovskite crystallization. In this work, we propose a stable precursor ink design strategy to control the solvent volatilization and perovskite crystallization to enable the wide speed window printing (0.3 to 18.0 m/min) of phase-pure FAPbI3 perovskite solar cells (pero-SCs) in ambient atmosphere. The FAPbI3 perovskite precursor ink uses volatile acetonitrile (ACN) as the main solvent with DMF and DMSO as coordination additives is beneficial to improve the ink stability, inhibit the coffee rings, and the complicated intermediate FAPbI3 phases, delivering high-quality pin-hole free and phase-pure FAPbI3 perovskite films with large-scale uniformity. Ultimately, small-area FAPbI3 pero-SCs (0.062 cm2 ) and large-area modules (15.64 cm2 ) achieved remarkable efficiencies of 24.32 % and 21.90 %, respectively, whereas the PCE of the devices can be maintained at 23.76 % when the printing speed increases to 18.0 m/min. Specifically, the unencapsulated device exhibits superior operational stability with T90 >1350 h. This work represents a step towards the scalable, cost-effective manufacturing of perovskite photovoltaics with both high performance and high throughput.

Volatile Perovskite Precursor Ink Enables Window Printing of Phase‐Pure FAPbI3 Perovskite Solar Cells and Modules in Ambient Atmosphere

AbstractDespite the great success of perovskite photovoltaics in terms of device efficiency and stability using laboratory‐scale spin‐coating methods, the demand for high‐throughput and cost‐effective solutions remains unresolved and rarely reported because of the complicated nature of perovskite crystallization. In this work, we propose a stable precursor ink design strategy to control the solvent volatilization and perovskite crystallization to enable the wide speed window printing (0.3 to 18.0 m/min) of phase‐pure FAPbI3 perovskite solar cells (pero‐SCs) in ambient atmosphere. The FAPbI3 perovskite precursor ink uses volatile acetonitrile (ACN) as the main solvent with DMF and DMSO as coordination additives is beneficial to improve the ink stability, inhibit the coffee rings, and the complicated intermediate FAPbI3 phases, delivering high‐quality pin‐hole free and phase‐pure FAPbI3 perovskite films with large‐scale uniformity. Ultimately, small‐area FAPbI3 pero‐SCs (0.062 cm2) and large‐area modules (15.64 cm2) achieved remarkable efficiencies of 24.32 % and 21.90 %, respectively, whereas the PCE of the devices can be maintained at 23.76 % when the printing speed increases to 18.0 m/min. Specifically, the unencapsulated device exhibits superior operational stability with T90>1350 h. This work represents a step towards the scalable, cost‐effective manufacturing of perovskite photovoltaics with both high performance and high throughput.

Promoting AEM Water Electrolyzer Performance and Reproducibility by Tumbler Milling of Ni3fe-LDH OER Catalyst

Anion exchange membrane water electrolysis is an attractive clean energy technology for producing hydrogen for energy storage, transport 1,2 and numerous other applications. Rational choice of highly active and stable catalysts as well as the proper design of catalyst layers are crucial to achieve technical relevance of electrolyser systems. The establishment of clear understanding of optimal catalyst treatment and methods of implementation are key steps towards optimized electrolyzer performance and durability. One aspect of catalyst performance in catalyst layers is the catalyst size distribution. A multimodal size distribution of catalyst particles or agglomerates can jeopardize the layer homogeneity and thus electrode performance.In this work, the effect of high-energy ball tumbling milling on the promising Ni3Fe-LDH OER catalyst followed by catalyst dispersion control was correlated to the microstructure of the catalyst layer, the achieved catalyst activity and utilization, and the resulting single cell performance and stability. Physico-chemical characterization confirmed the stable layered double hydroxide structure of the catalyst. By milling, a 300-fold reduction of catalyst agglomerate size, and an 8.8-fold increase of the geometrical surface was achieved. The optimized solvent compositions effectively increased the catalyst ink stability. We found that a significantly decreased catalyst agglomerate size resulted in very homogeneous mixtures of catalyst and ionomer. By tailoring the electrode structure design, lower internal electronic resistances of the electrodes, decreased charge-transfer resistances (Rct) of the membrane electrode assembly, and stable single cell durability of 1000 h with a minor degradation rate of 57 µV h-1 were accomplished.This work presents a facile and scalable approach of NiFe-LDH catalyst treatment and dispersion control and provides a guideline to follow for further electrode development and increased AEM water electrolyzer performances. References (1) Hydrogen Applications. Hydrogen Europe. 2020. https://hydrogeneurope.eu/hydrogen-applications (accessed Jan 7, 2022).(2) Vincent, I.; Bessarabov, D. Low Cost Hydrogen Production by Anion Exchange Membrane Electrolysis: A Review. Renew. Sustain. Energy Rev. 2018, 81 (August 2016), 1690–1704. https://doi.org/10.1016/j.rser.2017.05.258. This work has been performed in the frame of the CHANNEL project. This project has received funding from the Fuel Cells and Hydrogen 2 Joint Undertaking (now Clean Hydrogen Partnership) under grant agreement No 875088. This Joint undertaking receives support from the European Union's Horizon 2020 Research and Innovation program, Hydrogen Europe and Hydrogen Europe Research.

Eco-friendly alkali lignin-assisted water-based graphene oxide ink and its application as a resistive temperature sensor

Inkjet-printable ink formulated with graphene oxide (GO) offers several advantages, including aqueous dispersion, low cost, and environmentally friendly production. However, water-based GO ink encounters challenges such as high surface tension, low wetting properties, and reduced ink stability over prolonged storage time. Alkali lignin, a natural surfactant, is promising in improving GO ink’s stability, wettability, and printing characteristics. The concentration of surfactant additives is a key factor in fine-tuning GO ink’s stability and printing properties. The current study aims to explore the detailed effects of alkali lignin concentration and optimize the overall properties of graphene oxide (GO) ink for drop-on-demand thermal inkjet printing. A meander-shaped temperature sensor electrode was printed using the optimized GO ink to demonstrate its practical applicability for commercial purposes. The sensing properties are evaluated using a simple experimental setup across a range of temperatures. The findings demonstrate a significant increase in zeta potential by 25% and maximum absorption by 84.3%, indicating enhanced stability during prolonged storage with an optimized alkali lignin concentration compared to the pure GO dispersions. The temperature sensor exhibits a remarkable thermal coefficient of resistance of 1.21 within the temperature range of 25 °C–52 °C, indicative of excellent sensitivity, response, and recovery time. These results highlight the potential of alkali lignin as a natural surfactant for improving the performance and applicability of inkjet-printable GO inks in various technological applications.

Stable PbS colloidal quantum dot inks enable blade-coating infrared solar cells

Infrared solar cells are more effective than normal bandgap solar cells at reducing the spectral loss in the near-infrared region, thus also at broadening the absorption spectra and improving power conversion efficiency. PbS colloidal quantum dots (QDs) with tunable bandgap are ideal infrared photovoltaic materials. However, QD solar cell production suffers from small-area-based spin-coating fabrication methods and unstable QD ink. Herein, the QD ink stability mechanism was fully investigated according to Lewis acid–base theory and colloid stability theory. We further studied a mixed solvent system using dimethylformamide and butylamine, compatible with the scalable manufacture of method-blade coating. Based on the ink system, 100 cm2 of uniform and dense near-infrared PbS QDs (~ 0.96 eV) film was successfully prepared by blade coating. The average efficiencies of above absorber-based devices reached 11.14% under AM1.5G illumination, and the 800 nm-filtered efficiency achieved 4.28%. Both were the top values among blade coating method based devices. The newly developed ink showed excellent stability, and the device performance based on the ink stored for 7 h was similar to that of fresh ink. The matched solvent system for stable PbS QD ink represents a crucial step toward large area blade coating photoelectric devices.Graphical

Effect of poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) on low-iridium catalyst layer for proton exchange membrane water electrolysis

Reducing iridium loading in membrane electrode assembly (MEA) without sacrificing electrochemical performance plays a critical role in lowering the cost of proton exchange membrane water electrolyzers. However, low Ir loading often results in insufficient percolation of IrO2 particles and high interfacial resistance between the catalyst layer and the porous transport layer, causing reduced electrochemical performance and long-term durability issues. Herein, a MEA incorporating the conductive polymers of poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) as a binder and dispersant is investigated under 0.3 mgIr cm−2 loading. The zeta potential and morphological experiments confirm that the incorporation of PEDOT:PSS to the catalyst ink can improve the ink stability, reduce the catalyst particle size and create more pores in the catalyst layer. The MEA using a 1:1 ratio of PEDOT:PSS to Nafion achieves an enhanced current density of 1.68 V@1.0 A cm−2 at 80 °C (vs. a MEA using Nafion only, 1.75 V@1.0 A cm−2). The Raman results indicate that the PEDOT in the presence of Nafion exhibits a more conductive quinoid resonance structure than PEDOT. In situ durability testing of the MEA for over 800 h demonstrates a degradation rate of 48.7 μV h−1 at 1.0 A cm−2 and 80 °C.

Linking Multicomponent Interactions of Catalyst Ink and Catalyst Layer Fabrication with Electrochemical CO2 Reduction Performance

The controllable fabrication of catalyst layers (CL) by tuning the multiscale structure formation is complex but vital to achieving optimum CO2 reduction (CO2R) performance. The CL formation is deeply influenced by catalyst ink. An in-depth understanding on the role of each catalyst ink component and how multicomponent interactions affect ink status, catalyst layer structure, and CO2R performance is crucial.In this work, the roles of various ingredients of catalyst ink were systematically investigated from simple binary inks to complete catalyst inks. Our results showed Ag agglomerates can be broken down more efficiently in water than in alcohols due to stronger inter-particle repulsive forces induced by water disassociation. Ag particles-Nafion networks were found to play a decisive role in stabilizing catalyst ink, mitigating agglomeration and particle sintering. The catalyst ink was comprehensively characterized and reported by static multiple light scattering (SMLS) for the first time in this study. The evolution of catalyst ink was identified in three stages: stable, flocculation and sedimentation. Isopropanol (IPA)-rich solvents were demonstrated to be more effective in stabilizing catalyst ink due to better dispersed Nafion aggregates and further enhanced Ag particle-Nafion interactions.Subsequently, catalyst layer structure and CO2R performance were correlated with multi-component interactions in catalyst ink. Strong Ag particle-Nafion interactions were proven to promote not only ink stability, but also catalyst layer homogeneity and reaction site distribution. Water-rich inks helped improve the porosity and durability of GDEs. The cathodic potential of GDEs made by 70%-water inks (-0.75 V vs. NHE) was 30% lower than zero-water inks (-1.1 V vs. NHE), and the highest CO selectivity was boosted to 97% at an industrial meaningful current density of 200 mA/cm2 by enhancing Ag particle-Nafion interactions through rational design of ink formulation, dispersing and fabrication processes.Simultaneously, a scalable manufacturing methodology of robust GDE was developed and validated to achieve optimal CO2R performance. It will not only provide a meaningful reference for lab applications (fast and reproducible GDE fabrication aiming at new catalysts, ionomers, membranes or operation conditions development), but also provide a steppingstone to industrial applications (GDE fabrication aiming at large scale, good durability and quality of conformance). Figure 1

(Invited) Catalysts, Inks and Electrodes for PEM Water Electrolysis: Scalable Approach for Highly Performed Catalyst Layer Fabrication

The majority of commercially available anodic electrocatalysts for Low Temperature PEM Water Electrolyzers are based on unsupported iridium-based materials. These electrocatalysts can be amorphous or crystalline metallic, oxidic, and/or hydroxide-derived compounds. The planned worldwide installations of electrolyzers (on the order of tens of Gigawatts per year) will require manufacturing of Membrane Electrode Assemblies (MEAs) via highly scalable methods, one of which is Roll-2-Roll production (R2R) [1, 2]. In contrast to spraying techniques, R2R requires the utilization of inks with a higher content of solids, which in the case of extremely dense Ir-based materials may cause a sedimentation of suspended electrocatalysts resulting in overall ink destabilization.In the presented work a systematic study of ink stability with commercial IrO2 catalysts over a period of 14 days was performed. During this period of time the minimal redispersion of slurries was done to mimic realistic conditions of inks aging. The inks were comprehensively characterized by rheological measurements, zeta potential, particle size distribution (Dynamic Light Scattering) and inks density. A series of decal electrodes was fabricated using Baker bar coating approach (a model of R2R production) and coatings were characterized by contact angle, X-Ray Photoelectron Spectroscopy and Transmission Electron Microscopy.Detailed electrochemical performance analysis including the separation of voltage losses [3] via Electrochemical Impedance Spectroscopy was performed to compare MEA performance with aging time. Acknowledgements and Statements. The authors acknowledge financial support from M2FCT and H2NEW consortia. References. [1] J. Sharma, X. Lyu, T. Reshetenko, G. Polizos, K. Livingston, J. Li, D. L. Wood, A. Serov "Catalyst layer formulations for slot-die coating of PEM fuel cell electrodes" Int. Journal of Hydrogen Energy 47 (2022) 35838-3585.[2] E. B. Creel, K. Tjiptowidjojo, J. A. Lee, K. M. Livingston, P. R. Schunk, N. S. Bell, A. Serov, D. L. Wood III "Slot-Die-Coating Operability Windows for Polymer Electrolyte Membrane Fuel Cell Cathode Catalyst Layers" J. of Colloid and Interface Science 610 (2022) 474-485.[3] A. Dizon et. al “Advanced Voltage Break Down Analysis by Statistical Open-Source Tool Case Study Based on Polymer Electrolyte Water Electrolysis”, ECS 242 (2022)

Influence of the Electrode Deposition Method of Graphene-Based Catalyst Inks for ADEFC on Performance.

The utilization of graphene as a catalyst support has garnered significant attention due to its potential for enhancing fuel cell performance. However, a critical challenge in electrode production still lies in the electrode preparation technologies and the restacking of graphene sheets, which can greatly impact the fuel cell performance alongside with catalyst development. This study aimed to investigate the impact of different electrode deposition methods for N-rGO-based catalyst inks on catalyst layer morphology, with a specific focus on graphene sheet orientation and its influence on the performance of alkaline direct ethanol fuel cells (ADEFCs). The dispersion behavior and ink stability of the catalysts were assessed using ultraviolet-visible light (UV-vis), ζ potential, and dynamic light scattering techniques. The morphology and physical properties of the gas diffusion electrodes (GDEs) were analyzed through Brunauer-Emmett-Teller measurements, contact angle measurements and scanning electron microscopy (SEM) combined with energy-dispersive spectroscopy. The electrochemical behavior was evaluated both ex-situ, utilizing half-cell GDE measurements, and in situ, through single-cell tests. The N-rGO-based membrane electrode assembly, comprising Pt-free catalysts and a biobased membrane, exhibited outstanding performance in ADEFCs, as evidenced by high maximum power density values and long-term durability. The N-rGO-based membrane electrode assembly has demonstrated remarkable potential for high-performance fuel cells, presenting an exciting avenue for further exploration.

The role of resin in optimizing the performance and printing properties of water-based inkjet inks for food packaging

Purpose This study aims to investigate the influence of commercially available resins in water-based magenta pigment inkjet ink formulations on the properties of ink printability and the characteristics of ink application in food packaging. The impact of the resin on the jettability of the existing printability phase diagrams was also assessed. Design/methodology/approach Inks with different resin loadings were tested for selected properties, such as viscosity, particle size and surface tension. Stability was determined using a Turbiscan AGS turbidimeter and LumiFuge photocentrifuge analyzer. The ink layer fastness against abrasion and foodstuffs was evaluated using an Ugra device and according to PN-EN 646, respectively. JetXpert was used to assess Ricoh printhead jetting performance. Findings Printability diagrams successfully characterized the jettability of polyurethane inkjet inks on a multi-nozzle printhead and the binder improved droplet formation and printing precision. Originality/value Magenta water-based inkjet inks with commercial resins have been developed for printing on paper substrates. To the best of the authors’ knowledge, for the first time, inkjet ink stability was evaluated using the Turbiscan AGS and LumiFuge analyzers, and jettability models were verified using an industrial multi-nozzle printhead.

Preparation of fluorescent ink using perylene-encapsulated silica nanoparticles toward authentication of documents

Novel inorganic–organic hybrid fluorescent ink was produced for anticounterfeiting applications. Pigment/resin ink formulations were prepared from the thermally and photostable fluorescent perylene-doped silica nanoparticles (PSN). To create a colorless printed film from pigment/resin ink, the fluorescent perylene must be physically disseminated without clumping. Using screen-printing technique, the pigment/resin combination was successfully applied to sheets of cellulose paper. CIE Lab tests showed that pigment concentrations as low as 1 % result in a red emission when a uniform fluorescent layer was produced on the pale yellow cellulose paper surface. These printed sheets displayed an absorption band at 436 nm and an emission band at 625 nm. The fluorescent PSN exhibited diameters of 6–33 nm. The printed paper sheet was analyzed using various spectroscopic techniques, including scanning electron microscopy (SEM), infrared spectroscopy (FT-IR), energy-dispersive X-ray (EDX), and wavelength dispersive X-ray fluorescence (WDXRF). Upon repeated exposure to UV light, the prints exhibited a reversible fluorescence. Investigations into the ink rheological characteristics, stability, and printability were conducted.

Influence of the Nature of Aminoalcohol on ZnO Films Formed by Sol-Gel Methods

Here we present comparative studies of: (i) the formation of ZnO thin films via the sol-gel method using zinc acetate dihydrate (ZAD), 2-methoxyethanol (ME) as solvent, and the aminoalcohols (AA): ethanolamine, (S)-(+)-2-amino-1-propanol, (S)-(+)-2-amino-3-methyl-1-butanol, 2-aminophenol, and aminobenzyl alcohol, and (ii) elemental analyses, infrared spectroscopy, X-ray diffraction, scanning electron microscopy, absorption and emission spectra of films obtained after deposition by drop coating on glass surface, and thermal treatments at 300, 400, 500 and 600 °C. The results obtained provide conclusive evidences of the influence of the AA used (aliphatic vs. aromatic) on the ink stability (prior to deposition), and on the composition, structures, morphologies, and properties of films after calcination, in particular, those due to the different substituents, H, Me, or iPr, and to the presence or the absence of a -CH2 unit. Aliphatic films, more stable and purer than aromatic ones, contained the ZnO wurtzite form for all annealing temperatures, while the cubic sphalerite (zinc-blende) form was also detected after using aromatic AAs. Films having frayed fibers or quartered layers or uniform yarns evolved to "neuron-like" patterns. UV and photoluminescence studies revealed that these AAs also affect the optical band gap, the structural defects, and photo-optical properties of the films.

Correlating catalyst ink design and catalyst layer fabrication with electrochemical CO2 reduction performance

The controllable fabrication of catalyst layers (CL) by tuning the multiscale structure formation is complex but vital to achieving optimum carbon dioxide reduction (CO2R) performance. An in-depth understanding on the role of each catalyst ink component and how multi-component interactions affect ink status, catalyst layer structure, and CO2R performance is crucial. In this work, the roles of different ingredients of catalyst ink were systematically investigated from simple binary inks to complete catalyst inks. Silver (Ag) particles-Nafion interactions were found to play a decisive role in stabilizing catalyst ink, mitigating agglomeration and particle sintering. The catalyst ink was comprehensively characterized and reported by static multiple light scattering (SMLS) for the first time in this paper. The evolution of catalyst ink was identified in three stages: stable, flocculation and sedimentation. Isopropanol (IPA)-rich solvents were found to be more effective in stabilizing catalyst ink due to better dispersed Nafion aggregates and further enhanced Ag particle-Nafion interactions. Subsequently, catalyst layer structure and CO2R performance were correlated with multi-component interactions in catalyst ink. Strong Ag particle-Nafion interactions were proven to promote not only ink stability, but also catalyst layer homogeneity and reaction site distribution. The carbon monoxide (CO) selectivity was boosted from 80.5 % to 94 % at an industrial meaningful current density of 200 mA/cm2 using commercial Ag nanoparticles by rational design of ink formulation, dispersing and fabrication processes. Simultaneously, a scalable manufacturing methodology of robust gas diffusion electrodes (GDEs) to achieve optimal CO2R performance was developed and validated.