Molybdenum disulfide (MoS 2 ) with excellent properties has been widely reported in recent years. However, it is a great challenge to achieve p-type conductivity in MoS 2 because of its native stubborn n-type conductivity. Substitutional transition metal doping has been proved to be an effective approach to tune their intrinsic properties and enhance device performance. Herein, we report the growth of Nb-doping large-area monolayer MoS 2 by a one-step salt-assisted chemical vapor deposition method. Electrical measurements indicate that Nb doping suppresses ntype conductivity in MoS 2 and shows an ambipolar transport behavior after annealing under the sulfur atmosphere, which highlights the p-type doping effect via Nb, corresponding to the density functional theory calculations with Fermi-level shifting to valence band maximum. This work provides a promising approach of two-dimensional materials in electronic and optoelectronic applications.

This paper describes a new strategy for fabricating continuous gold films based on the self-assembly of the gold colloid monolayer on a poly(diallyldimethylammonium chloride)-modified glass slide, followed by electroless plating. Hydroxylamine-mediated reduction was proven as an excellent route to enlargement of immobilized nanoparticles on polymer-coated glass substrates in comparison to formaldehyde-mediated reduction. Au colloidal surface-catalyzed reduction of Au3+ by hydroxylamine exhibited very fast kinetics as monitored and confirmed by UV−vis spectroscopy in real time. The nanoscale morphology of the gold film was dependent on the initial coverage of gold nanoparticles and thermal annealing. Atomic force micrographs further revealed that enlarged particles were neither spherical nor cyclindrical, but highly complex in shape. The gold film thickness and its corresponding surface roughness could be easily controlled by setting the electroless deposition time. X-ray diffraction certified uniformity of deposits with the Au(111) crystallographic structure as the predominant one. No organic contamination during the course of electroless plating was observed as confirmed by both X-ray photoelectron spectroscopy and contact angle measurements. The stable and continuous gold films were used as electrodes for electrochemical experiments.

We report and discuss how gold nanoparticles were synthesized by the reduction of hydrogen tetrachloroaurate(III) trihydrate by sodium citrate in the presence of unmodified α-cyclodextrin (CD), β-CD, and γ-CD. Gold nanoparticles were immobilized on poly(diallyldimethylammonium) chloride (PDDA) modified glass slides to enable AFM measurements. The particle size was dependent upon the type and concentration of cyclodextrin used as well as the sodium citrate concentration. An increase in the cyclodextrin concentration effected a shift of the particle size range from 12−15 to 4−6 nm with uniform particle size distribution. The homogeneity of the synthesized gold nanoparticles was also evident from transmission electron micrographs (TEMs). Synthesis of gold nanoparticles by the reduction of hydrogen tetrachloroaurate(III) trihydrate by sodium borohydride in the presence of cyclodextrins also reduced the particle size from 6−8 to 2−4 nm. The consecutive particle growth due to the mutual coalescence between nanoclusters and their neighboring free gold atoms was limited in the presence of CDs. FT-Raman, FT-IR spectroscopy, and mass spectrometry (MS) indicated that the synthesis procedure exhibited no effect on the cyclodextrins. There was no evidence that gold nanoparticles were included in the CD cavities.

We present results of density functional theory (DFT) calculations of the adsorption of hydrogen molecules on Ti-decorated graphene. Our results indicate that the binding energies of molecular hydrogen on Ti-decorated graphene can be dramatically enhanced to 0.23-0.60 eV. The hybridization of the Ti 3d orbitals with the H(2) σ and σ* orbitals plays a central role in the enhanced binding. There is also a contribution from the attractive interaction between the surface dipole and the dipole of polarized H(2). It can be expected that Ti-decorated graphene could be considered as a potential high-capacity hydrogen storage medium.

Boron doped diamond (BDD) macro- and microelectrodes were modified by electrodeposition of platinum nanoparticles using a multipotential step electrodeposition technique and used for the oxidative determination of arsenite, As(III). The formation of Pt nanoparticles was evident from cyclic voltammetry measurement, whereas AFM and SEM revealed the size and size distribution of deposited Pt nanoparticles. Raman spectroscopy illustrated a correlation between the typical BDD signature and the number of platinum deposition cycles. Linear sweep voltammetry performed with the modified BDD microelectrode outperformed its macrocounterpart and resulted in very low detecting currents with enhanced signal-to-noise ratios. With linearity up to 100 ppb and a detection limit of 0.5 ppb, the electrochemical system was applicable for processing tap and river water samples. Over 150 repetitive runs could be performed, and electrochemical etching of platinum allowed the reuse of the BDD microelectrode. The presence of copper and chloride ions, the two most severe interferents at levels commonly found in groundwater, did not interfere with the assay.

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N-Acetyltyramine was synthesized and electropolymerized together with a negatively charged sulfobutylether-β-cyclodextrin on a boron-doped diamond (BDD) electrode followed by the electropolymerization of pyrrole to form a stable and permselective film for selective dopamine detection. The selectivity and sensitivity of the formed layer-by-layer film was governed by the sequence of deposition and the applied potential. Raman results showed a decrease in the peak intensity at 1329 cm−1 (sp3), the main feature of BDD, upon each electrodeposition step. Such a decrease was correlated well with the change of the charge-transfer resistance derived from impedance data, i.e., reflecting the formation of the layer-by-layer film. The polycrystalline BDD surface became more even with lower surface roughness as revealed by scanning electron and atomic force microscopy. The modified BDD electrode exhibited rapid response to dopamine within 1.5−2 s and a low detection limit of 4−5 nM with excellent reproducibility. Electroactive interferences caused by 4-dihydroxyphenylalanine, 3,4-dihydroxyphenylacetic acid, ascorbic acid, and uric acid were completely eliminated, whereas the signal response of epinephrine and norepinephrine was significantly suppressed by the permselective film.

Selective elimination of unwanted synapses is vital for the precise formation of neuronal circuits during development, but the underlying mechanisms remain unclear. Using inositol 1,4,5-trisphosphate receptor type 2 knockout (Itpr2−/−) mice to specifically disturb somatic Ca2+ signaling in astrocytes, we showed that developmental elimination of the ventral posteromedial nucleus relay synapse was impaired. Interestingly, intracerebroventricular injection of ATP, but not adenosine, rescued the deficit in synapse elimination in Itpr2−/− mice. Further studies showed that developmental synapse elimination was also impaired in P2ry1−/− mice and was not rescued by ATP, indicating a possible role of purinergic signaling. This hypothesis was confirmed by MRS-2365, a selective P2Y1 agonist, could also rescue the deficient of synapse elimination in Itpr2−/− mice. Our results uncovered a novel mechanism suggesting that astrocytes release ATP in an IP3R2-dependent manner to regulate synapse elimination.DOI: http://dx.doi.org/10.7554/eLife.15043.001