Dip-pen patterning of poly(9,9-dioctylfluorene) chain-conformation-based nano-photonic elements
Nature Communications Springer Nature 6 (2015) 1-9
Abstract:
Metamaterials are a promising new class of materials, in which sub-wavelength physical structures, rather than variations in chemical composition, can be used to modify the nature of their interaction with electromagnetic radiation. Here we show that a metamaterials approach, using a discrete physical geometry (conformation) of the segments of a polymer chain as the vector for a substantial refractive index change, can be used to enable visible wavelength, conjugated polymer photonic elements. In particular, we demonstrate that a novel form of dip-pen nanolithography provides an effective means to pattern the so-called β-phase conformation in poly(9,9-dioctylfluorene) thin films. This can be done on length scales ≤500 nm, as required to fabricate a variety of such elements, two of which are theoretically modelled using complex photonic dispersion calculations.Interplay between solid state microstructure and photophysics for poly(9,9‐dioctylfluorene) within oriented polyethylene hosts
Journal of Polymer Science Part B Polymer Physics Wiley 53:1 (2015) 22-38
High‐efficiency, solution‐processed, multilayer phosphorescent organic light‐emitting diodes with a copper thiocyanate hole‐injection/hole‐transport layer
Advanced Materials Wiley 27:1 (2014) 93-100
Abstract:
Copper thiocyanate (CuSCN) is introduced as a hole‐injection/hole‐transport layer (HIL/HTL) for solution‐processed organic light‐emitting diodes (OLEDs). The OLED devices reported here with CuSCN as HIL/HTL perform significantly better than equivalent devices fabricated with a PEDOT:PSS HIL/HTL, and solution‐processed, phosphorescent, small‐molecule, green OLEDs with maximum luminance ≥10 000 cd m‐2, maximum luminous efficiency ≤50 cd A‐1, and maximum luminous power efficiency ≤55 lm W‐1 are demonstrated.
High-speed scanning thermal lithography for nanostructuring of electronic devices.
Nanoscale 6:11 (2014) 5813-5819
Abstract:
We report a detailed analysis on the use of simultaneous substrate heating in conjunction with scanning thermal lithography (SThL) to dramatically increase the patterning speed of conventional SThL systems. The investigation consists of finite element simulations as well as practical assessments of the speed at which different organic precursors are thermally converted to produce standalone electrically active and passive nanostructures. As a proof of concept the high-speed SThL method was used to pattern semiconducting pentacene nanoribbons, which were subsequently incorporated into functioning transistors. Simultaneous substrate heating was found to allow patterning of functional devices at writing speeds >19 times higher than transistors produced at identical speeds but with the substrate maintained at room temperature. These fast written transistors exhibit 100× higher hole mobility with high on/off current ratio and negligible operating hysteresis. The generality of the proposed high-speed SThL method was further demonstrated with the rapid patterning of conductive nanostructured metal electrodes with excellent spatial resolution employing an appropriate polymer precursor as the chemical resist. It is proposed that these advances further support the case for using SThL systems as rapid prototypers for low micron and nanoscale structures for both direct patterning of precursors and indirect patterning of metals and other materials using suitable chemical resist.Wavefront kinetics of plasma oxidation of polydimethylsiloxane: limits for sub-μm wrinkling.
Soft matter 10:8 (2014) 1155-1166