Topological insulators display unique properties, such as the quantum spin Hall effect, because time-reversal symmetry allows charges and spins to propagate along the edge or surface of the topological insulator without scattering. However, the direct manipulation of these edge/surface states is difficult because they are significantly outnumbered by bulk carriers. Here, we report experimental evidence for the modulation of these surface states by using a gate voltage to control quantum oscillations in Bi(2)Te(3) nanoribbons. Surface conduction can be significantly enhanced by the gate voltage, with the mobility and Fermi velocity reaching values as high as ~5,800 cm(2) V(-1) s(-1) and ~3.7 × 10(5) m s(-1), respectively, with up to ~51% of the total conductance being due to the surface states. We also report the first observation of h/2e periodic oscillations, suggesting the presence of time-reversed paths with the same relative zero phase at the interference point. The high surface conduction and ability to manipulate the surface states demonstrated here could lead to new applications in nanoelectronics and spintronics.

We demonstrated a facile route for one-pot synthesis of visible light responsive nitrogen doped anatase TiO(2) sheets with dominant {001} facets from TiN. The synthesized anatase TiO(2) sheets show a strong and stable capability of generating photocatalysis active species of *OH radicals and hydrogen evolution from splitting water under visible light irradiation.

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Constructing photocatalytically favorable surface structure in synthesizing photocatalysts plays an important role in enhancing the photocatalytic activity of semiconductor photocatalysts. In this report, oxygen-deficient anatase TiO2 sheets with dominant {001} facets were synthesized via a facile one-pot hydrothermal route with solid metallic titanium diboride as precursor. In contrast to anatase TiO2 sheets with dominant {001} facets free of oxygen deficiency and surface fluorine, anatase TiO2 sheets with oxygen deficiency and surface fluorine are subject to obvious surface reconstruction as evidenced by two new Raman-active modes at 155 and 171 cm−1 and the weakened B1g mode at 397 cm−1. Further analysis based on X-ray photoelectron spectroscopy (XPS) spectra of Pt 4f and F 1s provided a clear evidence for the greatly strengthened interaction between Pt-loaded and TiO2 matrix as a result of a special electron-transfer process on the reconstructed surface structure of TiO2 with both oxygen deficiency and fluorine. Importantly, the reconstructed surface structure as well as the strengthened interaction between Pt-loaded and TiO2 matrix can substantially enhance the hydrogen evolution rate from photocatalytic water splitting reactions.

Developing highly efficient electrocatalysts based on cheap and earth-abundant metals for CO 2 reduction is of great importance. Here we demonstrate that the electrocatalytic activity of manganese-based heterogeneous catalyst can be significantly improved through halogen and nitrogen dual-coordination to modulate the electronic structure of manganese atom. Such an electrocatalyst for CO 2 reduction exhibits a maximum CO faradaic efficiency of 97% and high current density of ~10 mA cm −2 at a low overpotential of 0.49 V. Moreover, the turnover frequency can reach 38347 h −1 at overpotential of 0.49 V, which is the highest among the reported heterogeneous electrocatalysts for CO 2 reduction. In situ X-ray absorption experiment and density-functional theory calculation reveal the modified electronic structure of the active manganese site, on which the free energy barrier for intermediate formation is greatly reduced, thus resulting in a great improvement of CO 2 reduction performance.

The confined synthesis of two-dimensional covalent organic framework (2D COF) thin films was developed by using thin superspreading water on the hydrogel immersed under oil as reactor. Through loading two monomers into oil and hydrogel, respectively, COF thin films are synthesized at the oil/water/hydrogel interface. This strategy provides a new way for synthesis of freestanding 2D COF thin films. Detailed characterizations of the COF thin films reveal homogeneous topography, large area, controllable thickness from 4 to 150 nm, and crystallinity with certain orientation. Young's modulus of COF film is measured by AFM indentation as 25.9 ± 0.6 GPa, showing good mechanical properties. On the basis of the freestanding COF films, a nanofilter membrane and photoelectrochemical sensors for Ru were successfully developed. Moreover, the strategy was extended to the synthesis of crystalline zeolitic imidazolate framework-8 thin film, which exhibited high application potential.

Ammonia borane (AB) has attracted tremendous interest for on‐board hydrogen storage due to its low molecular weight and high gravimetric hydrogen capacity below a moderate temperature. However, the slow kinetics, irreversibility, and formation of volatile materials (trace borazine and ammonia) limit its practical application. In this paper, a new catalytic strategy involved lithium (Li) catalysis and nanostructure confinement in mesoporous carbon (CMK‐3) for the thermal decomposition of AB is developed. AB loaded on the 5% Li/CMK‐3 framework releases ∼7 wt % of hydrogen at a very low temperature (around 60 °C) and entirely suppresses borazine and ammonia emissions that are harmful for proton exchange membrane fuel cells. The possible mechanism for enhanced hydrogen release via catalyzed thermal decomposition of AB is discussed.