Maik R. J. Scherer

Mimicking the colourful wing scale structure of the Papilio blumei butterfly.

The brightest and most vivid colours in nature arise from the interaction of light with surfaces that exhibit periodic structure on the micro- and nanoscale. In the wings of butterflies, for example, a combination of multilayer interference, optical gratings, photonic crystals and other optical structures gives rise to complex colour mixing. Although the physics of structural colours is well understood, it remains a challenge to create artificial replicas of natural photonic structures. Here we use a combination of layer deposition techniques, including colloidal self-assembly, sputtering and atomic layer deposition, to fabricate photonic structures that mimic the colour mixing effect found on the wings of the Indonesian butterfly Papilio blumei. We also show that a conceptual variation to the natural structure leads to enhanced optical properties. Our approach offers improved efficiency, versatility and scalability compared with previous approaches.

A Nanostructured Electrochromic Supercapacitor

We report the first successful application of an ordered bicontinuous double-gyroid vanadium pentoxide network in an electrochromic supercapacitor. The freestanding vanadia network was fabricated by electrodeposition into a voided block copolymer template that had self-assembled into the double-gyroid morphology. The highly ordered structure with 11.0 nm wide struts and a high specific surface to bulk volume ratio of 161.4 μm(-1) is ideal for fast and efficient lithium ion intercalation/extraction and faradaic surface reactions, which are essential for high energy and high power density electrochemical energy storage devices. Supercapacitors made from such gyroid-structured vanadia electrodes exhibit a high specific capacitance of 155 F g(-1) and show a strong electrochromic color change from green/gray to yellow, indicating the capacitors charge condition. The nanostructuring approach and utilizing an electrode material that has intrinsic electrochemical color-change properties are concepts that can be readily extended to other electrochromic intercalation compounds.

Enhanced Electrochromism in Gyroid‐Structured Vanadium Pentoxide

Manufacturing V(2)O(5) in a 3D periodic highly interconnected gyroid structure on the 10 nm length scale is shown to lead to a significant electrochromic performance enhancement. The structured devices surpass previous inorganic electrochromic materials in all relevant parameters: the switching speed, coloration contrast, and composite coloration efficiency. In particular, the 85 ms switching speed lies within a factor of two of video rate. Enhanced ion intercalation into the gyroid morphology can be extended to other transition-metal oxides and is therefore promising for lithium ion batteries, supercapacitors, and sensors.

Efficient electrochromic devices made from 3D nanotubular gyroid networks.

Ion intercalation processes into metal oxide porous materials benefit from a high surface-to-volume ratio, while electronic charge transport requires a continuous network morphology. Detailed control over structure formation on the 10 nm length scale is therefore an effective strategy to enhance performance in electrochromic devices, supercapacitors, and batteries. Here we demonstrate the transformation of nickel patterned in a three-dimensional, highly interconnected, periodic nanomorphology into a self-supporting nickel oxide array with hollow struts. The oxidation of nickel gives rise to the nanoscale Kirkendall effect, which substantially increases the surface area of the NiO gyroid framework, without sacrificing its connectivity. Applicable to a vast range of electroplatable metals, this is a versatile route to high surface area metal oxides/chalcogenides which is especially suitable for various thin film applications. Nanostructured NiO electrodes showed substantially enhanced electrochromic performance, combining fast switching speeds with high coloration contrast.

Polymer Crystallization as a Tool To Pattern Hybrid Nanostructures: Growth of 12 nm ZnO Arrays in Poly(3-hexylthiophene)

Well-ordered hybrid materials with a 10 nm length scale are highly desired. We make use of the natural length scale (typically 10-15 nm) of the alternating crystalline and amorphous layers that are generally found in semicrystalline polymers to direct the growth of a semiconducting metal oxide. This approach is exemplified with the growth of ZnO within a carboxylic acid end-functionalized poly(3-hexylthiophene) (P3HT-COOH). The metal-oxide precursor vapors diffuse into the amorphous parts of the semicrystalline polymer so that sheets of ZnO up to 0.5 μm in size can be grown. This P3HT-ZnO nanostructure further functions as a donor-acceptor photovoltaic system, with length scales appropriate for charge photogeneration.

Labyrinth‐Induced Faceted Electrochemical Growth

A path-length bias of nucleated electrochemical growth in a 3D periodic nano-maze is found to cause facet formation of an intrinsically isotropic material in a porous self-assembled gyroid network. This is the first report of faceted electrochemical growth that is not based on the crystallographic order of the constituent building blocks, but rather reflects the symmetry of the template in which the material is synthesized.

Electropolymerization of Conjugated Polymers

This chapter investigates the nanostructuration of intrinsically conducting polymers via templated electropolymerization using polymeric scaffolds with a double-gyroid morphology.

Gyroid and Gyroid-Like Surfaces

This chapter gives an overview of the fascinating gyroid and gyroid-like surfaces, which are found in nature as intermaterial dividing surfaces. The single- and double-gyroid surfaces in particular will be discussed. In order to visualize these gyroidal structures the concept of a level surface will be introduced and applied

Visualization of energy: light dose indicator based on electrochromic gyroid nano-materials

The typical applications of electrochromic devices do not make use of the charge-dependent, gradual optical response due to their slow voltage-sensitive coloration. However, in this paper we present a design for a reusable, self-powered light dose indicator consisting of a solar cell and a gyroid-structured nickel oxide (NiO) electrochromic display that measures the cumulative charge per se, making use of the efficient voltage-sensitive coloration of gyroid materials. To circumvent the stability issues associated with the standard aqueous electrolyte that is typically accompanied by water splitting and gas evolution, we investigate a novel nano-gyroid NiO electrochromic device based on organic solvents of 1,1,1,3,3,3-hexafluoropropan-2-ol, and room temperature ionic liquid (RTIL) triethylsulfonium bis(trifluoromethylsulfonyl) imide ([SET3][TFSI]) containing lithium bis(trifluoromethylsulfonyl) imide. We show that an effective light dose indicator can be enabled by nano-gyroid NiO with RTIL; this proves to be a reliable device since it does not involve solvent degradation or gas generation.

Atomic Layer Deposition of Metal Oxides

With a current record conversion efficiency of 12.3 %, dye-sensitized solar cells (DSSCs) cannot quite yet compete with their conventional solid-state counterparts.