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The use of biodegradable and nontoxic cellulose as a renewable alternative to plastic in electronics is a promising way to decrease the environmental pollution. Unfortunately, cellulose lacks one o...

Monolithic aerogels composed of crystalline nanoparticles enable photocatalysis in three dimensions, but they suffer from low mechanical stability and it is difficult to produce them with complex geometries. Here, an approach to control the geometry of the photocatalysts to optimize their photocatalytic performance by introducing carefully designed 3D printed polymeric scaffolds into the aerogel monoliths is reported. This allows to systematically study and improve fundamental parameters in gas phase photocatalysis, such as the gas flow through and the ultraviolet light penetration into the aerogel and to customize its geometric shape to a continuous gas flow reactor. Using photocatalytic methanol reforming as a model reaction, it is shown that the optimization of these parameters leads to an increase of the hydrogen production rate by a factor of three from 400 to 1200 µmol g−1 h−1. The rigid scaffolds also enhance the mechanical stability of the aerogels, lowering the number of rejects during synthesis and facilitating handling during operation. The combination of nanoparticle-based aerogels with 3D printed polymeric scaffolds opens up new opportunities to tailor the geometry of the photocatalysts for the photocatalytic reaction and for the reactor to maximize overall performance without necessarily changing the material composition. ISSN:1613-6810 ISSN:1613-6829

The development of visible light-active photocatalysts is essential for increasing the conversion efficiency of solar energy into hydrogen (H2). Here, we present a facile method for nitrogen doping of monolithic titanium dioxide (TiO2) nanoparticle-based aerogels to activate them for visible light. Plasma-enhanced chemical vapor deposition at low temperature enables efficient incorporation of nitrogen into preformed TiO2 aerogels without compromising their advantageous intrinsic characteristics such as large surface area, extensive porosity, and nanoscale properties of the semiconducting building blocks. By balancing the dopant concentration and the defects, the nitridation improves optical absorption and charge separation efficiency. The nitrogen-doped TiO2 nanoparticle-based aerogels loaded with palladium (Pd) nanoparticles show a significant enhancement in visible light-driven photocatalytic H2 production (3.1 mmol h–1 g–1) with excellent stability over 5 days. With this method, we introduce a powerful tool to tune the properties of nanoparticle-based aerogels after synthesis for a specific application, as exemplified by visible light-driven H2 production. ISSN:1944-8244 ISSN:1944-8252

The development of visible light-active photocatalysts is essential for increasing the conversion efficiency of solar energy into hydrogen (H

Nanoparticle-based aerogels are 3-dimensional (3D) assemblies of macroscopic size that maintain the intrinsic properties of the initial nanoparticles. Accordingly, they bear immense potential to become an emerging platform for designing new and efficient photocatalysts. However, to take full advantage of this strategy, understanding of the multiscale processes occurring in such 3D-architectures is essential. Here, we prepared aerogels by co-assembling spherical Au, Pd, and PdAu with TiO2 nanoparticles and investigated their photocatalytic properties for hydrogen generation. During gelation, the anatase nanoparticles undergo oriented attachment, homogeneously entrapping the metal nanoparticles in the growing network. The aerogels offer a high porosity with a mean pore size of ca. 34 nm and a large surface area of about 450 m2 g−1. The porous structure enhances the light-harvesting, reagent transport, and electron migration process, generating 3.5-fold more hydrogen in comparison to the corresponding powders., Applied Catalysis B: Environmental, 267, ISSN:1873-3883, ISSN:0926-3373

Photocatalytic gas phase reactions represent a less explored yet promising direction within the highly active research area of photocatalysis. While photocatalytic liquid phase reactions are typically performed in water, photocatalytic gas phase reactions focus on gaseous and vaporized compounds. With this change in reaction environment, it is possible to address completely new questions and topics. Examples lie in the field of solar fuels, air pollution, global warming, and green chemistry. For this review, we selected five photocatalytic gas phase reactions, namely the reduction of CO2, water splitting, the oxidation of volatile organic compounds, the degradation of nitrogen oxides, and the synthesis of ammonia, which we discuss in the context of why they are important from a scientific, technological, and also societal point of view. We present the chemical mechanisms behind these photocatalytic processes and propose ideas and strategies for how these processes can be made more efficient. Our literatur...

We report a solution-phase approach to the synthesis of crystalline copper nanowires (Cu NWs) with an aspect ratio >1000 via a new catalytic mechanism comprising copper ions. The synthesis involves the reaction between copper(II) chloride and copper(II) acetylacetonate in a mixture of oleylamine and octadecene. Reaction parameters such as the molar ratio of precursors as well as the volume ratio of solvents offer the possibility to tune the morphology of the final product. A simple low-cost spray deposition method was used to fabricate Cu NW films on a glass substrate. Post-treatment under reducing gas (5% H2 + 95% N2) atmosphere resulted in Cu NW films with a low sheet resistance of 24.5 Ω/sq, a transmittance of T = 71% at 550 nm (including the glass substrate), and a high oxidation resistance. Moreover, the conducting Cu NW networks on a glass substrate can easily be transferred onto a polycarbonate substrate using a simple hot-press transfer method without compromising on the electrical performance. Th...

Chemical design criteria for materials for bioelectronics applications using a series of copolymer derivatives based on poly(3-hexylthiophene) are established. Directed chemical design via side-chain functionalization with polar groups allows manipulation of ion transport and ion-to-electron transduction. Insights gained will permit increased use of the plethora of materials employed in the organic electronics area for application in the bioelectronics field.