纳米棒
材料科学
分解水
热液循环
X射线光电子能谱
光电流
基质(水族馆)
化学工程
光催化
石墨氮化碳
可见光谱
纳米技术
光电子学
化学
催化作用
有机化学
地质学
工程类
海洋学
作者
Yuangang Li,Rongrong Wang,Huajing Li,Xiaoliang Wei,Juan Feng,Kaiqiang Liu,Yongqiang Dang,Anning Zhou
标识
DOI:10.1021/acs.jpcc.5b05427
摘要
Co-Pi decorated TiO2@graphitic carbon nitrides (g-C3N4) nanorod arrays (denoted as CCNRs) with different mass ratios of g-C3N4 have been constructed on the FTO substrate through three processes, hydrothermal growth, chemical bath deposition and electrodeposition. First, TiO2 nanorod arrays were grown onto a FTO substrate by a hydrothermal method. Second, g-C3N4 was coated onto the TiO2 nanorod arrays by immersing the above substrate with TiO2 nanorod arrays into a solution of urea and then heated at higher temperature. In this procedure, the amount of the g-C3N4 on the TiO2 nanorod arrays can be controlled by tuning the concentration of the urea solution. At last, Co-Pi were decorated on the surface of the TiO2@g-C3N4 by electrodeposition. The as-prepared CCNRs were characterized by XRD, FESEM, TEM, XPS, UV–vis, and FTIR, respectively, which illustrated that Co-Pi moieties were successfully decorated on the hybrid TiO2@g-C3N4 nanorod arrays. Photoelectrochemical (PEC) measurements have demonstrated that the prepared CCNRs serve as an efficient and stable photoanode for PEC seawater splitting. The photocurrent density reaches 1.6 mA/cm2 under 100 mW/cm2 (AM1.5G) light illumination at 1.23 V (RHE). More significantly, the CCNRs photoanode is quite stable during seawater splitting and the performance remain undiminished even after 10 h continuous illumination. Finally, a systematical photocatalytic mechanism of the Co-Pi decorated TiO2@g-C3N4 was proposed, and it can be considered as potential explanation of enhanced PEC performance.
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