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Tin dioxide (SnO 2 ) nanosheets/graphitic carbon nitride (g-C 3 N 4 ) composite was prepared by a hydrothermal method using mercapto acetic acid as the morphology directing agent in an acidic medium. The as-obtained composite was characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscope, and X-ray photoelectron spectroscopy; the results of this study show that in the composite, SnO 2 nanosheets with a thickness in the range ∼20–25 nm dispersed well on the g-C 3 N 4 . The lithium storage capability of the composite was investigated. The cycling performance of the composite was improved and is believed to be attributed by the presence of g-C 3 N 4 support.

The demand for well-designed nanostructured composites with enhanced electrochemical performance for lithium-ion batteries electrode materials has been emerging. In order to improve the electrochemical performance of MoS2-based anode materials, MoS2 nanosheets integrated with g-C3N4 (MoS2/g-C3N4 composite) was synthesized by a facile heating treatment from the precursors of thiourea and sodium molybdate at 550 &deg, C under N2 gas flow. The structure and composition of MoS2/g-C3N4 were confirmed by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis and elemental analysis. The lithium storage capability of the MoS2/g-C3N4 composite was evaluated, indicating high capacity and stable cycling performance at 1 C (A&middot, g&minus, 1) with a reversible capacity of 1204 mA&middot, h&middot, 1 for 200 cycles. This result is believed the role of g-C3N4 as a supporting material to accommodate the volume change and improve charge transport for nanostructured MoS2. Additionally, the contribution of the pseudocapacitive effect was also calculated to further clarify the enhancement in Li-ion storage performance of the composite.

Graphitic g-C3N4-WO3 composite was synthesized simply by decomposing melamine in the presence of WO3 at 500 o C. The obtained material was characterized by XRD, SEM, IR and XPS. The results showed that the as-prepared composite exhibits orthorhombic WO3 phase coated by g-C3N4 and the g-C3N4 decomposed completely with N-doped WO3 remaining at elevated calcination temperatures. The photocatalytic activity of the composite was evaluated by the photodegradation of methylene blue under visible light. An enhancement in photocatalytic activity for the graphitic g-C3N4-WO3 composite compared to the conventional nitrogendoped WO3 was observed, which can be attributed to the presence of g-C3N4 in the material.