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Graphene-analogue nanostructures defined as a new kind of promising materials with unique electronic, surface and optical properties have received much attention in the fields of catalysis, energy storage, sensing and electronic devices. Due to the distinctive structure characteristics of the graphene-analogue materials, they brought novel and amazing properties. Herein, graphene-analogue carbon nitride (GA-C₃N₄) was synthesized by high-yield, large-scale thermal exfoliation from the graphitic C₃N₄-based intercalation compound. Graphene-analogue carbon nitride exhibited 2D thin-layer structure with 6-9 atomic thickness, a high specific surface area of 30.1 m(2) g(-1), increased photocurrent responses and improved electron transport ability, which could give rise to enhancing the photocatalytic activity and stability. The graphene-analogue carbon nitride had a new features that could make it suitable as a sensor for Cu(2+) determination. So GA-C₃N₄ is a new but promising candidate for heavy metal ions (Cu(2+)) determination in water environment. The photocatalytic mechanism and photoelectrochemical selective sensing of Cu(2+) were also discussed.

Single-phased, high-color-rendering index (CRI) white-light phosphors are emerging as potential phosphor-converted white-light-emitting diodes (WLEDs) and as an alternative to blends of tricolor phosphors. However, it is a challenge to create a high CRI white light from a single-doped activator. Here, we present a high CRI (Ra = 91) white-light phosphor, Sr5(PO4)3-x(BO3)xCl:Eu2+, composed of Sr5(PO4)3Cl as the beginning member and Sr5(BO3)3Cl as the end member. This work utilized the solid-solution method, and tunable Eu2+ emission was achieved. Color-tunable Eu2+ emissions in response to structural variation were observed in Sr5(PO4)3-x(BO3)xCl solid solutions. This was further confirmed using X-ray Rietveld refinement, electron paramagnetic resonance spectroscopy, and in the photoluminescence spectra. The color-tunable emissions included the white light that originated from the combination of the blue emission of Sr5(PO4)3Cl:Eu2+ and an induced Eu2+ yellow emission at approximately 550 nm in the solid solution. Importantly, the white-light phosphors showed a greater R9 = 90.2 under excitation at 365 nm. This result has rarely been reported in the literature and is greater than that of (R9 = 14.3) commercial Y3Al5O12:Ce3+-based WLEDs. These findings demonstrate the great potential of Sr5(PO4)3-x(BO3)xCl:0.04Eu2+ as a white-light phosphor for near-UV phosphor-converted WLEDs. These results also provide a shortcut for developing a high CRI white-light phosphor from a single Eu2+-doped compound.

A novel, multi-walled carbon nanotubes (CNT) modified white C3N4 composite (CNT/white C3N4) with enhanced visible-light-response photoactivity was prepared. The white C3N4 and CNT combined together and formed the CNT/white C3N4 composite due to electrostatically-driven self-assembly with the hydrothermal method. The as-prepared white C3N4 and CNT/white C3N4 composite photocatalyst were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-vis absorption spectra, X-ray photoelectron spectroscopy (XPS) and photoluminescence spectroscopy (PL). The photoelectrochemical i-t curves were tested using several on-off cycles of light irradiation. The photoactivity of the catalysts was evaluated by degrading methylene blue (MB) dye solution. The results showed that the photoactivity for the degradation of MB solution was in the following order: CNT/white C3N4 composite > C3N4 > the white C3N4. The photoactivity of the CNT/white C3N4 composite was 66.5% and 34.5% higher than that of the white C3N4 sample and that of the C3N4 at 1.5 h, respectively. The degradation rate of the CNT/white C3N4 photocatalyst was almost 8.1 times as high as that of the white C3N4. The results indicated that CNT played an important role, which led to the efficient separation of the photo-generated charge carriers. The reason why the photoactivity of the CNT/white C3N4 was much higher than that of C3N4 and the white C3N4 was discussed. A possible mechanism of CNT on the enhancement of composites' visible light performance was also proposed.