In this communication the application of gold nanoparticle membranes as ambient pressure sensors with electromechanical signal transduction is demonstrated. The devices were fabricated by sealing microstructured cavities with membranes of 1,6-hexanedithiol cross-linked gold nanoparticles, which were electrically contacted by metal electrodes deposited on both sides of the cavities. Variations of the external pressure resulted in a deflection of the membranes and, thus, increased the average interparticle distances. Therefore, the pressure change could easily be detected by simply monitoring the resistance of the membranes.

In this article, highly sensitive differential pressure sensors based on freestanding membranes of cross-linked gold nanoparticles are demonstrated. The nanoparticle membranes are employed as both diaphragms and resistive transducers. The elasticity and the pronounced resistive strain sensitivity of these nanometer-thin composites enable the fabrication of sensors achieving high sensitivities exceeding 10 −3 mbar −1 while maintaining an overall small membrane area. Furthermore, by combining micro-bulge tests with atomic force microscopy and in situ resistance measurements the membranes' electromechanical responses are studied through precise observation of the concomitant changes of the membranes' topography. The study demonstrates the high potential of free-standing nanoparticle composites for the fabrication of highly sensitive force and pressure sensors and introduces a unique and powerful method for the electromechanical investigation of these materials.

Organic–Inorganic hybrids – from individual building blocks to an artificial carbon cycle and beyond.

Aerogels are highly porous solids that maintain the properties of individual nanomaterials at a macroscopic scale. However, the inability to fabricate hierarchical architectures limits technological implementation in energy storage, gas‐sorption, or catalysis. A 3D‐printing methodology for additive‐free TiO2 nanoparticle‐based aerogels is presented with full control of the nano‐, micro‐, and macroscopic length‐scales. To compensate for ink's low solid loading of 4.0 vol% and to enable subsequent processing into aerogels via supercritical drying, the printing is done in a liquid bath of alkaline pH. The 3D‐printing protocol retains a high specific surface area of 539 m2 g–1 and a mesopore diameter of 20 nm of conventionally casted aerogels while offering an unparalleled designability on the micrometer scale. To illustrate the new geometric freedom of 3D‐printed aerogels, the microstructure of a strongly light‐absorbing, photothermal Au‐nanorod/TiO2 aerogel is defined. To date, photothermal nanomaterials are mainly applied in the form of unstructured films where scalability is limited by light attenuation. Microstructures in 3D enhance light penetration by a factor of four and facilitate spatially defined heating on a macroscopic scale. The process can be generalized for a broad material library and allows to design inks with specific functionality, thus making aerogels adaptable for their target application.