Abstract

In the present work, N, S codoped TiO2 nano-crystallites (NCs) decorated TiO2 nano-tube arrays (N-S-TiO2 NCs/TNTAs) photoelectrodes have been successfully constructed through anodization method, followed by evaporation induced self-assembly (EISA) strategy. The structures of N-S-TiO2 NCs/TNTAs samples were characterized by scanning electrons microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron microscopy (XPS). Results indicated that TNTAs was partly covered by N, S codoped TiO2 NCs. Meanwhile, N elements coexisted in the forms of substitutional N (Ti–N and N–Ti–O) and interstitial N (Ti–O–N) in TiO2, while S elements were also incorporated into the lattice of TiO2 through substituting titanium atom and coexisted in the cationic forms of S6+ and S4+. In addition, optical and photoelectrochemical (PECH) properties of the as-prepared N-S-TiO2 NCs/TNTAs samples were investigated through UV–vis light diffuse reflection spectroscopy (DRS), transient open circuit potential (OCP), photocurrent response (PCR) and electro-chemical impedance spectroscopy (EIS). Furthermore, photodecomposition performances were evaluated by the yield of OH radicals and photocatalytic (PC) degradation of methyl blue (MB) under Xenon lamp irradiation. All results showed that N-S-TiO2 NCs/TNTAs photoelectrode exhibited intense visible light absorption ranging from 400 to 700nm, high transient photoinduced current of 0.115mAcm−2, open circuit photovoltage of −0.312mVcm−2, generation of hydroxyl radicals and PC efficiency of 59.7% for the degradation of MB. The enhanced PC performance could mainly be attributed to the decoration of N, S codoped TiO2 NCs, which could not only enhance the light absorption in visible region but also improve the transfer and separation efficiency of photoinduced charge carriers.

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