The building sector contributes approximately one third of the total energy consumption worldwide. A large part of this energy is used for the heating and cooling of buildings, which can be drastically reduced by use of energy-efficient glazing. In this study, we performed building energy simulations on a prototypical residential building, and compared commercially available static (low-e, solar IR blocking) to newly developed adaptive thermochromic glazing systems for various climate regions. The modeling results show that static energy-efficient glazing is mainly optimized for either hot climates, where low solar heat gain can reduce cooling demands drastically, or cold climates, where low-e properties have a huge influence on heating demands. For intermediate climates, we demonstrate that adaptive thermochromic glazing in combination with a low-e coating is perfectly suited. The newly developed thermochromic glazing can lead to annual energy consumption improvement of up to 22% in comparison to clear glass, which exceeds all other glazing systems. Furthermore, we demonstrate that in the Netherlands the use of this new glazing system can lead to annual cost savings of EU 638 per dwelling (172 m², 25% window façade), and to annual nationwide CO₂ savings of 4.5 Mt. Ergo, we show that further development of thermochromic smart windows into market-ready products can have a huge economic, ecological and societal impact on all intermediate climate region in the northern hemisphere.

For the preparation of electrically conductive composites, various combinations of cellulose and conducting materials such as polymers, metals, metal oxides and carbon have been reported. The conductivity of these cellulose composites reported to date ranges from 10⁻⁶ to 10³ S cm⁻¹. Cellulose nanocrystals (CNCs) are excellent building blocks for the production of high added value coatings. The essential process steps for preparing such coatings, i.e. surface modification of CNCs dispersed in water and/or alcohol followed by application of the dispersion to substrate samples using dip coating, are low cost and easily scalable. Here, we present coatings consisting of Ag modified CNCs that form a percolated network upon solvent evaporation. After photonic sintering, the resulting coatings are electrically conductive with an unprecedented high conductivity of 2.9 × 10⁴ S cm⁻¹. Furthermore, we report the first colloidal synthesis that yields CNCs with a high degree of Ag coverage on the surface, which is a prerequisite for obtaining coatings with high electrical conductivity.

Au and Ag nanoshells are of interest for a wide range of applications. The plasmon resonance of such nanoshells is the property of interest and can be tuned in a broad spectral regime, ranging from the ultraviolet to the mid-infrared. To date, a large number of manuscripts have been published on the optics of such nanoshells. Few of these, however, address the effect of particle size distribution and metal shell imperfections on the plasmon resonance. Both are inherent to the chemical synthesis of metal nanoshells and therefore to a large extent unavoidable. It is of vital importance to understand their effect on the plasmon resonance, since this determines the scope and limitations of the technology and may have a direct impact on the application of such particles. Here, we elucidate the effect of particle size distribution and imperfections in the metal shell on the plasmon resonance of Au and Ag nanoshells. The size of the polystyrene core and the thickness of the Au and Ag shells are systematically varied to study their influence on the plasmon resonance, and the results are compared to values obtained through optical simulations using extended Mie theory and finite element method. Discrepancies between theory and practice are studied in detail and discussed extensively. Quantitative information on the minimum thickness of the metal shell, which is required to realize a satisfactory plasmon resonance of a metal nanoshell, is provided for Au and Ag.

We present the synthesis of glucose-functionalized polystyrene particles through emulsion polymerisation using glucose acrylate as reactive surfactant. Additionally, we present the selective deposition of silver on the surface of these particles yielding well-defined polystyrene–silver composites.

Janus particles are of great research interest because of their reduced symmetry, which provides them with unique physical and chemical properties. Such particles can be prepared from spherical structures through colloidal assembly. Whilst colloidal assembly has the potential to be a low cost and scalable process, it typically lacks selectivity. As a consequence, it results in a complex mixture of particles of different architectures, which is tedious to purify. Very recently, we reported the colloidal synthesis of Au semishells, making use of polystyrene–polyphenylsiloxane Janus particles as an intermediate product (Chem. Commun. 2017, 53, 3898–3901). Here, we demonstrate that these Janus particles are realized through colloidal assembly of spherical glucose-functionalized polystyrene particles and an emulsion of phenyltrimethoxysilane in aqueous ammonia, followed by interfacial polycondensation to form the polyphenylsiloxane patch. Both the polystyrene spheres and the emulsion of Ph-TMS in aqueous ammonia are stabilized by a surfmer—a reactive surfactant. The colloidal assembly reported in this manuscript proceeds with an unexpected high selectivity, which makes this process exceptionally interesting for the synthesis of Janus particles. Furthermore, we report insights into the details of the mechanism of formation of these Janus particles, and apply those to adapt the synthesis conditions to produce polystyrene particles selectively decorated with multiple polyphenylsiloxane patches, e.g., raspberry particles.