光电流
分解水
材料科学
光激发
纳米棒
光电子学
能量转换效率
金红石
费米能级
光电化学电池
纳米技术
电极
光催化
化学
电解质
原子物理学
物理
物理化学
电子
催化作用
有机化学
激发态
量子力学
生物化学
作者
Jen-Chun Chou,Min‐Han Yang,Jung‐Wei Liao,Chi‐Young Lee,Jon-Yiew Gan
标识
DOI:10.1016/j.matchemphys.2013.11.056
摘要
TiO2 is one of the most promising photoanodes for solar-hydrogen conversion by water splitting. However, the solar-hydrogen efficiency of TiO2 remains limited because of a low photocurrent generation. A clear understanding of photoexcitations within photoanodes can predict the quantity of photocurrent and consequently determine the solar-hydrogen efficiency. In this work, hydrothermally synthesized rutile TiO2 nanorods were investigated for their photoelectrochemical (PEC) performance. A photogenerated hole concentration of TiO2 photoanode was derived as 8.40 × 1014 cm−3 under one sun illumination. In addition, Fermi level pinning associated with high density of surface states was also observed under PEC operation. Base on these results, a series of band diagrams of TiO2 photoanode were established to describe the photogeneration of holes and current at various bias potential. The main limitation of photocurrent generation is the distribution of surface-trapped states, which determines the hole concentration at the surface and consequently determines the open-circuit potential and the photocurrent density.
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