A mixture of bulk hexagonal boron nitride (h-BN) with hydrazine, 30% H(2)O(2), HNO(3)/H(2)SO(4), or oleum was heated in an autoclave at 100 °C to produce functionalized h-BN. The product formed stable colloid solutions in water (0.26-0.32 g L(-1)) and N,N-dimethylformamide (0.34-0.52 g L(-1)) upon mild ultrasonication. The yield of "soluble" h-BN reached about 70 wt%. The dispersions contained few-layered h-BN nanosheets with lateral dimensions in the order of several hundred nanometers. The functionalized dispersible h-BN was characterized by IR spectroscopy, X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, UV/Vis spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM). It is shown that h-BN preserves its hexagonal structure throughout the functionalization procedure. Its exfoliation into thin platelets upon contact with solvents is probably owing to the attachment of hydrophilic functionalities.

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Over the past decade, nanosized metal oxides, metals, and bimetallic particles have been actively researched as enzyme mimetic nanomaterials. However, the common issues with individual nanoparticles (NPs) are stabilization, reproducibility, and blocking of active sites by surfactants. These problems promote further studies of composite materials, where NPs are spread on supports, such as graphene derivatives or dichalcogenide nanosheets. Another promising type of support for NPs is the few-layered hexagonal boron nitride (hBN). In this study, we develop surfactant-free nanocomposites containing Pt NPs dispersed on chemically modified hydrophilic hBN nanosheets (hBNNSs). Ascorbic acid was used as a reducing agent for the chemical reduction of the Pt salt in the presence of hBNNS aqueous colloid, resulting in Pt/hBNNS nanocomposites, which were thoroughly characterized with X-ray diffraction, transmission electron microscopy, dynamic light scattering, and X-ray photoelectron and infrared spectroscopies. Similar to graphene oxide binding the metal NPs more efficiently than pure graphene, hydrophilic hBNNSs well stabilize Pt NPs, with particle size down to around 8 nm. We further demonstrate for the first time that Pt/hBNNS nanocomposites exhibit peroxidase-like catalytic activity, accelerating the oxidation of the classical colorless peroxidase substrate 3,3′,5,5′-tetramethylbenzidine (TMB) to its corresponding blue-colored oxidized product in the presence of H 2 O 2 . Kinetic and mechanism studies involving terephthalic acid and isopropanol as a fluorescent probe and an • OH radical scavenger, respectively, proved that Pt/hBNNSs assist H 2 O 2 decomposition to active oxygen species ( • OH), which are responsible for TMB oxidation. The Pt/hBNNS nanocomposite-assisted oxidation of TMB provides an effective platform for the colorimetric detection of dopamine, an important biomolecule. The presence of increased amounts of dopamine gradually inhibits the catalytic activity of Pt/hBNNSs for the oxidation of TMB by H 2 O 2 , thus enabling selective sensing of dopamine down to 0.76 μM, even in the presence of common interfering molecules and on real blood serum samples. The present investigation on Pt/hBNNSs contributes to the knowledge of hBN-based nanocomposites and discovers their new usage as nanomaterials with good enzyme-mimicking activity and dopamine-sensing properties.

Although many of the layered metal chalcogenides, such as MoS2, are well-studied, some other chalcogenides have received less attention by comparison. In particular, there has been an emerging interest in vanadium tetrasulfide (VS4), which displays useful properties as a component of hybrids. However, the synthetic methods and characteristics of individual VS4 are not yet well defined, and there is no report on its solution processability. Here we have synthesized VS4 by a simple and fast direct reaction between elements. Reinvestigation of the VS4 crystal structure yielded more precise atomic coordinates and interatomic distances, thereby confirming the crystallization of VS4 in the monoclinic C2/c group and its quasi-1D chainlike structure. As the chains in VS4 are only bonded by weak van der Waals forces, we further demonstrate that bulk VS4 may be ultrasonically dispersed in appropriate solvents to form colloids, similarly to the layered chalcogenides. VS4 particles in colloids retain their phase identity and rod-shaped morphology with lengths in the range of hundreds of nanometers. Isopropanol dispersion exhibited the highest concentration and stability, which was achieved owing to the repulsion caused by high negative charges on the edges of the particles.