We investigate the Goos-Hänchen-like shifts for Dirac fermions in transmission through a monolayer graphene barrier. The lateral shifts, as the functions of the barrier's width and the incidence angle, can be negative and positive in Klein tunneling and classical motion, respectively. Due to their relations to the transmission gap, the lateral shifts can be enhanced by the transmission resonances when the incidence angle is less than the critical angle for total reflection, while their magnitudes become only the order of Fermi wavelength when the incidence angle is larger than the critical angle. These tunable beam shifts can also be modulated by the height of potential barrier and the induced gap, which gives rise to the applications in graphene-based devices.

We have investigated the transmission in monolayer graphene barrier at non-zero angle of incidence. Taking the influence of parallel wave vector into account, the transmission as the function of incidence energy has a gap due to the evanescent waves in two cases of Klein tunneling and classical motion. The modulation of the transmission gap by the incidence angle, the height and width of potential barrier may lead to potential applications in graphene-based electronic devices.

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Defect-embedded chiral nematic organizations are attractive due to their light manipulation ability that is crucial for photonic applications. Self-assembly of cellulose nanocrystals (CNC) forms a left-handed chiral nematic structure, which makes simultaneous reflection of left-handed circularly polarized (LCP) and right-handed circularly polarized (RCP) light a challenging task. Herein, we present unprecedented evidence that self-organized CNC films with left-handed helical sense and photonic bandgaps (PBG) display ambidextrous CP light reflection with peak reflectivity up to 68% and transform spontaneous photoluminescence to RCP and LCP luminescence with respective |g lum | values up to 0.796 and 0.120. These ambidextrous chiroptical properties originate from a left-handed chiral nematic structure consisting of a nematic-like phase, acting as a half-wave retarder, sandwiched between two PBG layers. The latter are spontaneously intercalated into the left-handed helicoids by rapid gelation of CNC colloidal suspensions. We demonstrate that the ambidextrous chiroptical properties can be manipulated by changes in evaporation temperatures, concentrations, and characteristics of CNC suspensions. We showcase the potential of defect-embedded chiral nematic CNC films for the sustainable and scalable development of anti-counterfeiting optical labels.

Engineering hierarchical structures of electrode materials is a powerful strategy for optimizing the electrochemical performance of an anode material for lithium-ion batteries (LIBs). Herein, we report the fabrication of hierarchical TiO2/C nanocomposite monoliths by mediated mineralization and carbonization using bacterial cellulose (BC) as a scaffolding template as well as a carbon source. TiO2/C has a robust scaffolding architecture, a mesopore-macropore network and TiO2-C heterostructure. TiO2/C-500, obtained by calcination at 500 °C in nitrogen, contains an anatase TiO2-C heterostructure with a specific surface area of 66.5 m(2) g(-1). When evaluated as an anode material at 0.5 C, TiO2/C-500 exhibits a high and reversible lithium storage capacity of 188 mA h g(-1), an excellent initial capacity of 283 mA h g(-1), a long cycle life with a 94% coulombic efficiency preserved after 200 cycles, and a very low charge transfer resistance. The superior electrochemical performance of TiO2/C-500 is attributed to the synergistic effect of high electrical conductivity, anatase TiO2-C heterostructure, mesopore-macropore network and robust scaffolding architecture. The current material strategy affords a general approach for the design of complex inorganic nanocomposites with structural stability, and tunable and interconnected hierarchical porosity that may lead to the next generation of electrochemical supercapacitors with high energy efficiency and superior power density.

Hierarchical zeolite sponges with a nanotube scaffolding architecture, nanotube-trimodal connectivity and self-generated nanotubes with tunable geometry.

Higher-order organization of inorganic nanoparticles with hierarchical architectures and tailored functionality is crucial in the nanofabrication of advanced materials. Here we demonstrate that three-dimensional b-oriented MFI superstructures can be organized by synergistic chemical synthesis and self-assembly. The organization is accomplished by vapor treatment of tetrapropylammonium hydroxide (TPAOH)-coated inorganic/bacterial cellulose scaffolds. TPA acts to direct nucleation and to mediate crystal morphology leading to oriented assembly of MFI crystals along crystallographic b-axis, whereas bacterial cellulose holds the oriented assembly together forming three-dimensional superstructures with macroporosity. Self-supporting monoliths of the macroporous MFI show outstanding selective adsorption for para-xylene and high adsorption capacity for volatile organic compounds. Incorporating luminescent molecules imparts the macroporous monoliths the new property of adsorption tunable luminescence that may act as an optical sensor indicating the level of adsorption. The current work opens a novel space for rational organization of hierarchical materials with tailored architectures and multifunctionality.

Advances in zeolites research emerging from interdisciplinary efforts have opened new opportunities beyond conventional applications. Colloids drive much current research owing to their distinct collective behaviors, but so far, using zeolites as a colloidal building block to construct ordered superstructures remains unexplored. Herein we show that selfassembly of colloidal zeolite LTA superball (ZAS) by tiltedangle sedimentation forms macroscopic films with micromesoporosity and 3D long-range periodicity featuring a photonic band gap (PBG) that is tunable through the superball geometry and responds reversibly to chemical vapors. Remarkably, self-assembly of ZAS at elevated temperature forms 3D chiral photonic crystals that enable negative circular dichroism, selective reflection of right-handed circularly polarized (CP) light and left-handed CP luminescence based on PBG. We present a novel class of functional colloids and zeolite-based photonic crystals with the ability to manipulate light in several ways.