Mo 2 C, [ 5 ] MoB, [ 5 a] NiMoN x , [ 6 ] and Co 0.6 Mo 1.4 N 2 , [ 7 ] whereas for OER-layered double hydroxides (LDHs) containing nickle, [ 8 ] cobalt, [ 8 b, 9 ] and iron [ 8 a, c, 10 ] or their calcination-derived mixed metal oxide (MMO) nanocomposites show good and stable activities. [ 11 ] However, the majority of these electrocatalysts are either semiconducting or insulating, which greatly hinders electron transfer from the electrocatalyst to the support electrode, thereby restricting their overall effi ciency and utilization potential. Using a single bifunctional OER and HER catalyst can simplify the water splitting system and also lowers the cost. [ 12 ] However, this is challenging since the same material must be able to effectively catalyze both the OER and HER while achieving a low overall overpotential and as high a current density as possible. [ 13 ] Compared to oxides and hydroxides of a particular metal, metal nitrides often display superior water-splitting activities owing to their special properties such as low electrical resistance and good corrosion resistance. [ 14 ] Recently, the synthesis of Ni 3 N nanosheets was reported for the fi rst time, [ 15 ] which potentially could represent a new class of OER electrocatalyst with better properties than NiO. Compared with single-metal nitrides, the activity of double metal nitrides can more readily be optimized through a controlled manipulation of the valence and electronic states of the metal elements, resulting in enhanced water-splitting performance. [ 7 ] LDHs are a family of layered clays containing divalent and trivalent metal cations, which can include electrochemically active elements such as Ni, Fe, and Co amongst others. [ 16 ] LDH nanosheets with ultrathin atomic scale thickness can readily be synthesized using top-down or bottom-up approaches. [ 17 ] Thermal ammonolysis of LDH nanosheets could potentially lead to the formation of novel nanostructured mixed metal nitrides (MMNs) for electrocatalytic applications, though very little work has been conducted in this area to date. The viability of this approach for the rational design of nanostructured MMNs from LDH precursors for overall water splitting is systematically explored herein.In this work, Ni 3 FeN nanoparticles (Ni 3 FeN-NPs) with a particle size of 100 nm and a thickness of ≈9 nm are successfully synthesized by thermal ammonolysis of ultrathin NiFe-LDH nanosheets prepared using a reverse microemulsion method ( Scheme 1 ). The Ni 3 FeN-NPs exhibited extraordinarily high activities for both HER and OER with low overpotentials of 158 and 280 mV at 10 mA cm −2 , respectively, and Tafel slopes of 42 and 46 mV dec −1 , respectively. The remarkable electrocatalytic activity of Ni 3 FeN-NPs can be attributed to highly exposed active sites and high electrical conductivity. This work conclusively Demand for clean renewable energy will increase enormously over the next 50-100 years, driven by rapid human population growth, fast depletion of fossil fuel resources, and environmental ...

Nitrogen-doped graphene hydrogels (NGHs) were synthesized through a one-pot hydrothermal route with graphene oxide (GO) as raw material and urea as reducing-doping agents. The morphology, structure, and components of the NGHs were characterized by scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, methylene blue adsorption, thermogravimetric analysis and electrical conductivity measurements. The results demonstrated that nitrogen was doped into the graphene plane at the same time as the GO sheets were reduced, and the nitrogen content incorporated into the graphene lattice was in the range of 3.95 to 6.61 at.% with pyrrolic N as the main component. The NGHs contained about 97.6 wt% water and have a large specific surface area (SSA) of >1300 m 2 g À1 in the wet state. In addition, the electrochemical performance of the NGHs was investigated. The sample NGHs-4 with a nitrogen content of 5.86 at.% and SSA of 1521 AE 60 m 2 g À1 in the wet state showed excellent capacitive behavior (308 F g À1 at 3 A g À1 ) and superior cycling stability (92% retention after 1200 cycles) in 6 mol L À1 KOH. The experimental results indicated that not only the N-content but also the N-type have very significant impact on the capacitive behavior.Furthermore, NGHs strongly influenced the electrochemical properties because of their high SSAs and mesoporous structure.

The rapid quantification of the enantiomers of small chiral molecules is very important, notably in pharmacology. Here, we show that the enantiomers of drug molecules can be distinguished by stochastic sensing, a single-molecule detection technique. The sensing element is an engineered alpha-hemolysin protein pore, fitted with a beta-cyclodextrin adapter. By using the approach, the enantiomeric composition of samples of ibuprofen and thalidomide can be determined in less than 1 s.