Single Interdigital Transducer Approach for Gravimetrical SAW Sensor Applications in Liquid Environments.

Surface acoustic wave (SAW) devices are well known for mass-sensitive sensor applications. In biosensing applications, chemical and biochemically evoked binding processes on surfaces are detected in liquid environments using delay line or resonator sensor configurations, preferably in combination with the appropriate microfluidic devices. All configurations share the common feature of analyzing the transmission characteristic of the propagating SAW. In this paper, a novel SAW-based impedance sensor type is introduced which uses only one interdigital transducer (IDT), simultaneously as the SAW generator and the sensor element. Here, the input port reflection coefficient S11 is measured at the IDT instead of the commonly used S21 transmission forward gain parameter. Thus, a sharp and distinct peak of the S11 spectrum is obtained, enabling a comfortable direct readout of the sensor signal. Proof of the concept was gained by analyzing the specific binding of the 4-mercaptophenylacetic acid gold nanoparticles (MPA-AuNP) directly to the IDT surface. The corresponding binding kinetic of the MPA-AuNP on the functionalized gold surface has been analyzed and a sensitivity of 7.4 mΩ nM-1 has been determined.

Directed Self-Assembly and Infrared Reflection Absorption Spectroscopy Analysis of Amphiphilic and Zwitterionic Janus Gold Nanoparticles.

Here, we report an approach to use infrared reflection absorption spectroscopy (IRRAS) for the unambiguous proof of the presence as well as the spatial distribution of organic ligands on the Janus gold nanoparticle (AuNP) surface. For this purpose we synthesized amphiphilic and zwitterionic Janus AuNPs and immobilized these on pretreated gold surfaces by directed self-assembly, exploiting hydrophilic/hydrophobic or electrostatic interactions, respectively. Thus, we obtained macroscopic two-dimensional arrays of Janus AuNPs exhibiting a specific orientation. These arrays were investigated by IRRAS, and the obtained spectra revealed only peaks of the ligands facing the IR beam, while the ligands facing the gold substrate were not detected due to reflection of the IR beam on the AuNP cores. Thus, we describe a straightforward spectroscopic procedure to prove the Janus character of zwitterionic and amphiphilic AuNPs in the size range of 10-15 nm.

Differential adsorption of gold nanoparticles to gold/palladium and platinum surfaces.

Integration of molecule-capped gold nanoparticles (AuNP) into nanoelectronic devices requires detailed knowledge about the AuNP-electrode interface. Here, we report the pH-dependent adsorption of amine or carboxylic acid-terminated gold nanoparticles on platinum or gold/palladium (30% Pd) alloy, respectively. We synthesized amine-terminated AuNP, applying a new solid phase supported approach, as well as AuNP exhibiting carboxylic acid as terminal groups. The pH-induced agglomeration of the synthesized AuNP was investigated by UV-vis, DLS, and ζ-potential measurements. Depending on the pH and the ionic strength of the AuNP solution a preferential adsorption on the different metals occurred. Thereby, we demonstrate that by choosing the appropriate functional group and adjusting the pH as well as the ionic strength a directed binding can be achieved, which is an essential prerequisite for applications of these particles in nanoelectronics. These findings will pave the way for a controlled designing of the interface between molecule-capped AuNP and metallic electrodes for applications in nanoelectronics.

Impact of device design on the electronic and optoelectronic properties of integrated Ru-terpyridine complexes.

The performance of nanoelectronic and molecular electronic devices relies strongly on the employed functional units and their addressability, which is often a matter of appropriate interfaces and device design. Here, we compare two promising designs to build solid-state electronic devices utilizing the same functional unit. Optically addressable Ru-terpyridine complexes were incorporated in supramolecular wires or employed as ligands of gold nanoparticles and contacted by nanoelectrodes. The resulting small-area nanodevices were thoroughly electrically characterized as a function of temperature and light exposure. Differences in the resulting device conductance could be attributed to the device design and the respective transport mechanism, that is, thermally activated hopping conduction in the case of Ru-terpyridine wire devices or sequential tunneling in nanoparticle-based devices. Furthermore, the conductance switching of nanoparticle-based devices upon 530 nm irradiation was attributed to plasmon-induced metal-to-ligand charge transfer in the Ru-terpyridine complexes used as switching ligands. Finally, our results reveal a superior device performance of nanoparticle-based devices compared to molecular wire devices based on Ru-terpyridine complexes as functional units.