RESUMO
We demonstrate an understanding of different physicochemical properties of copolymers induced by systematic changes in their structural parameters, i.e., the chemical structure of the comonomer unit, composition, molecular weight, and dispersity. The terpolymers were designed to be implemented in a chemically amplified resist (CAR) to form negative-tone patterns. With two basic repeating units of 4-hydroxystyrene and 2-ethyl-2-methacryloxyadamantane as monomers for conventional CARs, the pendant group of the third methacrylate comonomer was varied from aromatic, aliphatic lactone to lactone rings to modulate the interaction capability of the copolymer chains with n-butyl acetate, which is a negative-tone developer. Along with these structures, the monomer composition, molecular weight, and dispersity were also controlled. Physicochemical properties of the synthesized copolymers having controlled structures, i.e., dissolution behaviors and quantified Hansen solubility parameters, surface wetting characteristics, and surface roughness, which can be important properties affecting patterning capability in high-resolution lithography, were explored. Furthermore, the feasibility to use experimentally determined Hansen solubility parameters of the copolymers for the prediction of pattern formation using a coarse-grained model was assessed. Our comprehensive studies on the correlation of the structural parameters of the copolymers with final properties offer fundamental avenues to attain effective designs of the complex CAR system toward the lithographic process to achieve a sub-10 nm dimension, which is close to a single-chain dimension.
RESUMO
The realization of high-efficiency solution-processed organic light-emitting diodes (OLEDs) using phosphorescent tetradentate Pt(II) emitters and bipolar organic hosts is demonstrated in this work. To investigate the effect of organic host on the platinum dopant, the performances of solution-processed Pt-OLEDs with various combinations between four tetradentate Pt(II) emitters, including two newly developed tetra-Pt-S2 and tetra-Pt-S3 and three bipolar organic hosts m-TPAPy, o-TPAPy, and o-CzPy, have been analyzed and compared. Among the tetradentate Pt(II) complexes studied in this work, tetra-Pt-S3 exhibited the best electroluminescent performance attributable to its bulky molecular scaffold structure, high emission quantum yield, and good solubility in common organic solvents. High external quantum efficiencies (EQEs) of up to 22.4% were achieved in the solution-processed OLED with tetra-Pt-S3 emitter and m-TPAPy host at the dopant concentration of 4 wt %. At a high luminance of 1000 cd m-2, the EQE of this device decreased slightly to 21.0%.
RESUMO
Thermally stable, strongly luminescent gold-TADF emitters are the clue to realize practical applications of gold metal in next generation display and lighting technology, a scarce example of which is herein described. A series of donor-acceptor type cyclometalated gold(III) alkynyl complexes with some of them displaying highly efficient thermally activated delayed fluorescence (TADF) with Φ up to 88% in thin films and emission lifetimes of ≈1-2 µs at room temperature are developed. The emission color of these complexes is readily tunable from green to red by varying the donor unit and cyclometalating ligand. Vacuum-deposited organic light-emitting diodes (OLEDs) with these complexes as emissive dopants achieve external quantum efficiencies (EQEs) and luminance of up to 23.4% and 70 300 cd m-2, respectively.
