2.1. Materials
Electroluminescent (EL) samples were fabricated by coating an interface layer, in the first step, and a sequential set of different layers, depicted in previous Error! Reference source not found., onto a supporting polyester (PES) textile, a fabric of weight 75 g/m2, consisting of a rectangular shape with dimensions 7x12 cm, and on a commercial polycarbonate (PC)/acrylonitrile-butadiene-styrene (ABS) rectangular plaque used as a control sample, with reference Pulse GX70 and dimensions 7x12 cm.
For the preparation of the inks and pastes, different polymers, solvents, fillers, and specific compounds were investigated. Regarding the preparation of the interface layer, Thermoplastic Polyurethane (TPU) pellets (Apilon 52® MA-6505, SpecialChem SA, Mussolente, Italy) were purchased; DMF (anhydrous, 99.8%) was purchased from Sigma-Aldrich (Missouri, USA) and THF (analytical reagent grade, >= 99.8%) was purchased from Fisher Chemical (Hampton, New Hampshire, USA). This interface layer was applied, by direct contact to polyester substrates, by knife coating technique, using the automatic film applicator coater ZAA 2300, from Zehntner GmbH Testing Instruments, Switzerland.
For the electroluminescent device structure, the coating technique adopted was spray coating. For that, a spray gun was obtained from Stardust (HVLP Spray Gun Kit, 4001, Stardust Colors SAS, St Laurent des Arbres, France). A nozzle diameter of 0.8mm, an air pressure of 1.38 - 1.72 bar, and a distance of 20 - 25 cm between the substrate and spray gun was used. To prevent harmful evaporation of the solvents, a painting cabin and fume hood were used during the ink deposition process.
To achieve the ACPEL device structure, the first layer, namely, the conductive bottom electrode, is applied on the central area of the sample surface and the busbar is coated around the illuminated area to provide a low resistance path for better current distribution. In this phase, a short circuit can occur at any point in time if the application process was not followed properly, more precisely, when the back electrode and busbar are touching each other somewhere within the ACPEL structure. During the coating process, minimum distance between both must be considered and it is about 4 mm.
For this formulation, related to back electrode and busbar, which are applied simultaneously by spray coating technique, semi-matt acrylic lacquer with direct adhesion on plastic was purchased from Lechler, Italy, more precisely, the acrylic base (LS947 2K Plastic grip), the hardener (29355 Lechsys Acritop standard hardener), and the diluent (00527 PC thinner). The silver nanoparticles, 35 nm, 99.5%, NM-0023-HP (IoLiTec-Ionic Liquids Technologies GmbH, from Germany), multi-layer graphene platelets PR0953 (Thomas Swan & Co. Ltd., from UK) and the conductive polymer polypyrrole doped, 5 wt% dispersion in H2O (Sigma Aldrich, from USA) were also used in different concentrations.
Regarding the insulating layer with a high dielectric constant, the same acrylic base, hardener, and diluent (Lechler, from Italy) were used and, finally, the barium titanate in powder, BT-301, was purchased (from WuXi Noble Electronics Co. Ltd, China).
For the phosphor layer, the base is the same, more precisely, the acrylic base, the hardener and the diluent (Lechler, from Italy) and the luminescent particles, LP-6844, were provided by LWB-Leuchtstoffwerk Breitungen GmbH, Germany. Regarding the commercial phosphor layer, a standard ink was acquired from Lumilor company (OH, USA), more precisely, the LC-B311-GR-Lumigreen, in order to produce a control sample. Finally, the top electrode layer, translucent material to allow light passage through, consists of the same solvents used in the interface layer, more precisely, DMF (anhydrous, 99.8%), purchased from Sigma-Aldrich (Missouri, USA), solvent THF (analytical reagent grade, >= 99.8%), provided by Fisher Chemical (Hampton, New Hampshire, USA) and the conductive polymer Clevios FE T, purchased to Heraeus Deutschland GmbH & Co. KG (Germany).
The composition of the phosphor layer was prepared with different ratios of zinc sulphide doped with copper, more precisely between 30.0 to 38.1 wt%, and also different amounts of diluent, between 28.0 to 35.5 wt%, according to Error! Reference source not found., presented below. For each formulation, the resulting ink was then magnetically stirred for twenty minutes, until a homogeneous solution was obtained.
Table 1.
Matrix plan of the experiments.
Table 1.
Matrix plan of the experiments.
Sample |
Designation |
Substrate |
Composition of phosphor ink |
ZnS:Cu (Wt%) |
Diluent (Wt%) |
1 |
S1 - 32.7% ZnS:Cu vs. 30.5% D |
PC/ABS |
32.7 % |
30.5 % |
2 |
S2 - 32.7% ZnS:Cu vs. 30.5% D |
PES |
32.7 % |
30.5 % |
3 |
S3 – Commercial ink |
PES |
LC-B311-GR-Lumigreen* |
4 |
S4 - 30.0% ZnS:Cu vs. 30.5% D |
PES |
30.0 % |
30.5 % |
5 |
S5 – 35.4% ZnS:Cu vs. 30.5% D |
PES |
35.4 % |
30.5 % |
6 |
S6 - 38.1% ZnS:Cu vs. 30.5% D |
PES |
38.1 % |
30.5 % |
7 |
S7 - 30.0% ZnS:Cu vs. 28.0% D |
PES |
30.0 % |
28.0 % |
8 |
S8 – 35.4% ZnS:Cu vs. 33.0% D |
PES |
35.4 % |
33.0 % |
9 |
S9 - 38.1% ZnS:Cu vs. 35.5% D |
PES |
38.1 % |
35.5 % |
2.2. Methods
After defining the matrix plan of the experiments, the main steps to prepare the formulations and to build the electroluminescent device are shown below.
For the phosphor ink, the main steps for formulation development, before the coating, can be observed below, in
Figure 2.
In order to create a process easily scalable, the main steps to build the electroluminescent device can be observed below, in
Figure 3.
The composition of the phosphor layer used for the development of an EL device was analyzed in terms of sample morphology, chemical composition and illuminance performance.
Morphological analyses were performed in an ultra-high-resolution Field Emission Gun Scanning Electron Microscopy (FEG-SEM), NOVA 200 Nano SEM; FEI Company (Hillsboro, OR, USA). Topographic images were obtained with a Secondary electron detector at an acceleration voltage of 10 kV. Before morphological analyses samples were covered with a thin film (35 nm) of Au-Pd (80-20 weight %), in a high-resolution sputter coater, 208HR Cressington Company, coupled to an MTM-20 Cressington High-Resolution Thickness Controller [
11].
Chemical analyses of samples were performed with the Energy Dispersive Spectroscopy (EDS) technique, using an EDAX Si (Li) detector at an acceleration voltage of 15 kV.
The illuminance values were measured with a light meter (Extech Instruments, New Hampshire, USA), LT300 model, up to 400 000 lux, with a high resolution of 0.01 Fc/lux. An average of three readings for each point was performed for each 9-12 standard spread point on the substrate surface.
Regarding the functionalized polyester substrates, the thickness of each EL layer was measured with a Mitutoyo 2046F dial indicator.