Noble metal electrocatalysts (e.g., Pt, Ru, etc.) suffer from sluggish kinetics of water dissociation for the electrochemical reduction of water to molecular hydrogen in alkaline and neutral pH environments. Herein, we found that an integration of Ru nanoparticles (NPs) on oxygen-deficient WO3-x manifested a 24.0-fold increase in hydrogen evolution reaction (HER) activity compared with commercial Ru/C electrocatalyst in neutral electrolyte. Oxygen-deficient WO3-x is shown to possess large capacity for storing protons, which could be transferred to the Ru NPs under cathodic potential. This significantly increases the hydrogen coverage on the surface of Ru NPs in HER and thus changes the rate-determining step of HER on Ru from water dissociation to hydrogen recombination.

Double halide perovskites are a class of promising semiconductors applied in photocatalysis, photovoltaic devices, and emitters to replace lead halide perovskites, owing to their nontoxicity and chemical stability. However, most double perovskites always exhibit low photoluminescence quantum efficiency (PLQE) due to the indirect bandgap structure or parity‐forbidden transition problem, limiting their further applications. Herein, the self‐trapped excitons emission of Cs2NaInCl6 by Sb‐doping, showing a blue emission with high PLQE of 84%, is improved. Further, Sb/Mn codoped Cs2NaInCl6 nanocrystals are successfully synthesized by the hot‐injection method, showing a tunable dual‐emission covering the white‐light spectrum. The studies of PL properties and dynamics reveal that an energy transfer process can occur between the self‐trapped excitons and dopants (Mn2+). The work provides a new perspective to design novel lead‐free double perovskites for realizing a unique white‐light emission.

The capture of sustainable energy from a salinity gradient, in particular, using renewable biomass-derived functional materials, has attracted significant attention. In order to convert osmotic energy to electricity, many membrane materials with nanofluidic channels have been developed. However, the high cost, complex preparation process, and low output power density still restrict the practical application of traditional membranes. Herein, we report the synthesis of highly flexible and mechanically robust nanofiber-arrays-based carbonaceous ordered mesoporous nanowires (CMWs) through a simple and straightforward softtemplating hydrothermal carbonization approach. This sequential superassembly strategy shows a high yield and great versatility in controlling the dimensions of CMWs with the aspect ratio changes from about 3 to 39. Furthermore, these CMWs can be used as novel building blocks to construct functional hybrid membranes on macroporous alumina. This nanofluidic membrane with asymmetric geometry and charge polarity exhibits low resistance and highperformance energy conversion. This work opens a solution-based route for the one-pot preparation of CMWs and functional heterostructure membranes for various applications.

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This work presents the growth of high-quality Ge epilayers on Si (001) substrates using a reduced pressure chemical vapor deposition (RPCVD) chamber. Based on the initial nucleation, a low temperature high temperature (LT-HT) two-step approach, we systematically investigate the nucleation time and surface topography, influence of a LT-Ge buffer layer thickness, a HT-Ge growth temperature, layer thickness, and high temperature thermal treatment on the morphological and crystalline quality of the Ge epilayers. It is also a unique study in the initial growth of Ge epitaxy; the start point of the experiments includes Stranski–Krastanov mode in which the Ge wet layer is initially formed and later the growth is developed to form nuclides. Afterwards, a two-dimensional Ge layer is formed from the coalescing of the nuclides. The evolution of the strain from the beginning stage of the growth up to the full Ge layer has been investigated. Material characterization results show that Ge epilayer with 400 nm LT-Ge buffer layer features at least the root mean square (RMS) value and it’s threading dislocation density (TDD) decreases by a factor of 2. In view of the 400 nm LT-Ge buffer layer, the 1000 nm Ge epilayer with HT-Ge growth temperature of 650 °C showed the best material quality, which is conducive to the merging of the crystals into a connected structure eventually forming a continuous and two-dimensional film. After increasing the thickness of Ge layer from 900 nm to 2000 nm, Ge surface roughness decreased first and then increased slowly (the RMS value for 1400 nm Ge layer was 0.81 nm). Finally, a high-temperature annealing process was carried out and high-quality Ge layer was obtained (TDD=2.78 × 107 cm−2). In addition, room temperature strong photoluminescence (PL) peak intensity and narrow full width at half maximum (11 meV) spectra further confirm the high crystalline quality of the Ge layer manufactured by this optimized process. This work highlights the inducing, increasing, and relaxing of the strain in the Ge buffer and the signature of the defect formation.

Biochars prepared in three pyrolysis atmospheres of N2, O2, and CO2 were investigated. The pyrolysis characteristics, pore structures, and functional groups of the biochars were characterized by thermogravimetric analysis (TGA), specific surface area and porosity analyses, and Fourier transform infrared (FTIR) spectroscopy. The adsorption mechanism was further explored by the temperature-programmed desorption (TPD) technique in combination with the adsorption kinetics. The results showed that the Hg0 adsorption capacities of the biochars produced in an O2 pyrolysis atmosphere were worse than those of the biochars obtained in a N2 atmosphere, whereas CO2 significantly promoted the adsorption capacity. The biochar prepared in 20% CO2 had the highest adsorption capacity. Three pyrolysis reaction pathways were possible in the O2 atmosphere. In addition, a critical concentration existed between O2 concentrations of 5 and 7%. Above 750 °C, CO2 could react directly with the biochar through the Boudouard reaction. Mercury adsorbed to the surface of the biochar in various ways in the mercury adsorption process and thus was attached to the surface of the biochar in several forms. The products of chemical adsorption were Hg-OM and HgO, and a “secondary adsorption layer” was proposed to form in the mechanism. In the process of mercury adsorption by the biochar, a small part of the Hg0 chemically adsorbed to the active sites through their functional groups, which were mainly carbonyl and carboxyl groups. At the same time, the formation of a monolayer or multilayer “secondary adsorption layer” occurred, and the remaining Hg0 could further adsorb to this “secondary adsorption layer”.