A cluster obtained in high yield from the reduction of a silver-thiolate precursor, Ag-SCH(2)CH(2)Ph, exhibited a single sharp peak near 25 kDa in the matrix-assisted laser desorption mass spectrum (MALDI MS) and a well-defined metal core of ~2 nm measured with transmission electron microscopy (TEM). The cluster yields a single fraction in high-performance liquid chromatography (HPLC). Increased laser fluence fragments the cluster until a new peak near 19 kDa predominates, suggesting that the parent cluster-Ag(152)(SCH(2)CH(2)Ph)(60)-evolves into a stable inorganic core-Ag(152)S(60). Exploiting combined insights from investigations of clusters and surface science, a core-shell structure model was developed, with a 92-atom silver core having icosahedral-dodecahedral symmetry and an encapsulating protective shell containing 60 Ag atoms and 60 thiolates arranged in a network of six-membered rings resembling the geometry found in self-assembled monolayers on Ag(111). The structure is in agreement with small-angle X-ray scattering (SAXS) data. The protective layer encapsulating this silver cluster may be the smallest known three-dimensional self-assembled monolayer. First-principles electronic structure calculations show, for the geometry-optimized structure, the development of a ~0.4 eV energy gap between the highest-occupied and lowest-unoccupied states, originating from a superatom 90-electron shell-closure and conferring stability to the cluster. The optical absorption spectrum of the cluster resembles that of plasmonic silver nanoparticles with a broad single feature peaking at 460 nm, but the luminescence spectrum shows two maxima with one attributed to the ligated shell and the other to the core.

We report the systematic appearance of a plasmon-like optical absorption feature in silver clusters protected with 2-phenylethanethiol (PET), 4-flurothiophenol (4-FTP) and (4-(t-butyl)benzenethiol (BBS) as a function of cluster size. A wide range of clusters, namely, Ag₄₄(4-FTP)₃₀, Ag₅₅(PET)₃₁, ∼Ag₇₅(PET)₄₀, ∼Ag₁₁₄(PET)₄₆, Ag₁₅₂(PET)₆₀, ∼Ag₂₀₂(BBS)₇₀, ∼Ag₄₂₃(PET)₁₀₅, and ∼Ag₅₃₀(PET)₁₀₀ were prepared. The UV/Vis spectra show multiple features up to ∼Ag₁₁₄; and thereafter, from Ag₁₅₂ onwards, the plasmonic feature corresponding to a single peak at ∼460 nm evolves, which points to the emergence of metallicity in clusters composed of ∼150 metal atoms. A minor blue shift in the plasmonic peak was observed as cluster sizes increased and merged with the spectrum of plasmonic nanoparticles of 4.8 nm diameter protected with PET. Clusters with different ligands, such as 4-FTP and BBS, also show this behavior, which suggests that the 'emergence of metallicity' is independent of the functionality of the thiol ligand.

A fuel cell based amperometric H2 sensor with pulsed electrodeposited electrodes has been developed and tested for its performance. Nafion, a commercial proton exchange membrane was used as electrolyte in the sensor. Platinum (Pt) deposited gas diffusion electrode (GDE) based sensing and counter electrodes were prepared by electrodeposition and pulsed electrodeposition methods using 1‐butyl‐3‐methylimidazolium tetrafluoroborate ionic liquid electrolyte. Prior to the electrodeposition, the electrodeposition behaviour of Pt on GDE was studied by cyclic voltammetry, chronoamperometry and chronopotentiometry. The deposition potential of Pt was obtained from cyclic voltammogram. The nucleation and growth behaviour of Pt were examined by chronopotentiometry and chronoamperometry. Electrodeposition and pulsed electrodeposition of Pt on GDE were carried out under the optimized conditions. The prepared electrodes were characterized by field emission scanning electron microscope and gracing incidence X‐ray diffraction. In order to compare the sensor performance, Nafion based amperometric hydrogen sensors were made with both electrodeposited and pulsed electrodeposited Pt on GDE electrodes. The assembled amperometric H2 sensors were tested in the dynamic range of 1–4% of H2/Ar. Pulsed electrodeposited Pt on GDE sensor showed higher sensitivity and better response time than the electrodeposited Pt on GDE sensor.