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To improve the photocatalytic activity of graphene-based catalysts, silicon phthalocyanine (SiPc) covalently functionalized N-doped ultrasmall reduced graphene oxide (N-usRGO) has been synthesized through 1,3-dipolar cycloaddition of azomethine ylides. The obtained product (N-usRGO/SiPc) was characterized by transmission electron microscopy, atomic force microscopy, Fourier transform infrared spectroscopy, Raman spectra, X-ray photoelectron spectroscopy, fluorescence, and UV-vis spectroscopy. The results demonstrate that SiPc has been successfully grafted on the surface of N-usRGO. The N-usRGO/SiPc nanocomposite exhibits high light-harvesting efficiency covering a range of wavelengths from the ultraviolet to visible light. The efficient fluorescence quenching and the enhanced photocurrent response confirm that the photoinduced electron transfers from the SiPc moiety to the N-usRGO sheet. Moreover, we chose Pt nanoparticles as cocatalyst to load on N-usRGO/SiPc sheets to obtain the optimal H2 production effect. The platinized N-usRGO/SiPc (N-usRGO/SiPc/Pt) demonstrates good hydrogen evolution performance under both UV-vis and visible light (λ>400 nm) irradiation. The apparent quantum yields are 1.3% and 0.56% at 365 and 420 nm, respectively. These results reveal that N-usRGO/SiPc/Pt nanocomposite, consolidating the advantages of SiPc, N-usRGO, and Pt NPs, can be a potential candidate for hydrogen evolution from water under UV-vis or visible light irradiation.

UV-assisted fabrication of In2O3 nanorods/reduced graphene oxide composites with enhanced interfacial charge transfer and photocatalytic performance under visible light.

By doping Cu­(I) ions in Zn0.3Cd0.7S, a novel p-type Cu doped Zn0.3Cd0.7S modified graphene (Zn0.3Cd0.7S (Cu)/GR) film photocathode was prepared. The as-prepared p-type Zn0.3Cd0.7S (Cu)/GR photocathode and an n-type WO3/graphene (WO3/GR) photoanode were used to assemble a photoelectrochemical tandem cell. Through examination of the optoelectronic and photoelectrochemical properties of Zn0.3Cd0.7S (Cu)/GR and WO3/GR photoelectrode, we evaluate the feasibility of the tandem cell for overall water splitting under UV–vis light irradiation. The optimal Cu doping in Zn0.3Cd0.7S photocathode concentration was found to be 6%. The rates of hydrogen and oxygen evolved from this tandem cell with the optimal electrodes were 65.6 and 12.3 μmol g–1 h–1 (80.5 and 15.1 μmol cm–2 h–1), respectively. This study suggests a promising method for constructing an efficient photoelectrochemical tandem device for overall water splitting.