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Electrochemical energy converters based on biomass-based organic molecules such as glucose have recently demonstrated great potential for the development of functional bioimplantable devices such as pacemakers, but such converters lack efficient metal-based anode nanocatalysts, which could combine the stability of parameters with high performance. Here, we elaborate a technique of femtosecond laser ablation in water to synthesize bare (ligand-free) PdAu alloy nanoparticles with constituents having a variable ratio and explore these nanoparticles as electrocatalysts for glucose oxidation. Our data evidence that the combination of two metals in one bare nanoformulation can result in a strong synergetic effect, which makes the combination of high catalytic activity toward glucose oxidation with ultrafast kinetics at low potentials possible due to the presence of Au and Pd, respectively, while a bare uncontaminated surface ensures outstanding catalytic performance. We show that at an optimal ratio of constituents (50%/50%), PdAu nanoparticles can provide a mass activity of 60 A g−1and an onset potential lower than 0.27 V vs.RHE, which outperform all currently existing nanoparticle-based electrodes. Our results show that bare nanomaterials prepared by laser-ablation synthesis can offer much improved characteristics as electrocatalysts for energy conversion and storage applications, while the versatility of laser synthesis can be extended to other alloy architectures in order to provide optimal characteristics for a concrete catalytic process.

When arranged in a proper nanoaggregate architecture, gold nanoparticles can offer controllable plasmon-related absorption/scattering, yielding distinct color effects that depend critically on the relative orientation and distance between nanoparticle constituents. Herein, we report on the implementation of novel plasmonic nanoarchitectures based on complexes between gold nanoparticles and an azobenzene-modified cationic surfactant that can exhibit a light-tunable plasmonic response. The formation of such complexes becomes possible through the use of strongly negatively charged bare gold nanoparticles (∼10-nm diameter) prepared by the method of laser ablation in deionized water. Driven by electrostatic interactions, the cationic surfactant molecules attach and form a shell around the negatively charged nanoparticles, resulting in neutralization of the particle charge or even overcompensation beyond which the nanoparticles become positively charged. At low and high surfactant concentrations, Au nanoparticles are negatively and positively charged, respectively, and are represented by single species due to electric repulsion effects having absorption peaks around 523–527 nm, whereas at intermediate concentrations, the Au nanoparticles become neutral, forming nanoscale 100-nm clusterlike aggregates and exhibiting an additional absorption peak at λ > 600 nm and a visible change in the color of the solution from red to blue. Because of the presence of the photosensitive azobenzene unit in the surfactant tail that undergoes trans-to-cis isomerization under irradiation with UV light, we then demonstrate a light-controlled nanoclustering of nanoparticles, yielding a switch in the plasmonic absorption band and a related change in the solution color. The formed hybrid architectures with a light-controlled plasmonic response could be important for a variety of tasks, including biomedical, surface-enhanced Raman spectroscopy (SERS), data transmission, and storage applications.