Department of Mechanical Engineering, Stanford University, California 94305, United States.
Nano Lett. 2011 Nov 9;11(11):4978-84. doi: 10.1021/nl2029392. Epub 2011 Oct 20.
We report a hierarchically branched TiO(2) nanorod structure that serves as a model architecture for efficient photoelectrochemical devices as it simultaneously offers a large contact area with the electrolyte, excellent light-trapping characteristics, and a highly conductive pathway for charge carrier collection. Under Xenon lamp illumination (UV spectrum matched to AM 1.5G, 88 mW/cm(2) total power density), the branched TiO(2) nanorod array produces a photocurrent density of 0.83 mA/cm(2) at 0.8 V versus reversible hydrogen electrode (RHE). The incident photon-to-current conversion efficiency reaches 67% at 380 nm with an applied bias of 0.6 V versus RHE, nearly two times higher than the bare nanorods without branches. The branches improve efficiency by means of (i) improved charge separation and transport within the branches due to their small diameters, and (ii) a 4-fold increase in surface area which facilitates the hole transfer at the TiO(2)/electrolyte interface.
我们报告了一种具有层次分支结构的 TiO2 纳米棒结构,作为高效光电化学器件的模型结构,它同时提供了与电解质的大接触面积、优异的光捕获特性以及电荷载流子收集的高导电性途径。在氙灯照射下(与 AM 1.5G 匹配的紫外线光谱,总功率密度为 88 mW/cm2),分支 TiO2 纳米棒阵列在相对于可逆氢电极(RHE)为 0.8 V 的偏压下产生 0.83 mA/cm2 的光电流密度。在施加 0.6 V 相对于 RHE 的偏压时,在 380nm 处的光生电流转换效率达到 67%,几乎是没有分支的裸纳米棒的两倍。分支通过以下方式提高效率:(i)由于其较小的直径,在分支内提高了电荷分离和传输;(ii)表面面积增加了 4 倍,这有利于在 TiO2/电解质界面处的空穴转移。