光电流
赤铁矿
重组
分解水
化学
电子
材料科学
化学物理
分析化学(期刊)
光化学
光电子学
光催化
物理
矿物学
生物化学
色谱法
量子力学
基因
催化作用
作者
Stephanie R. Pendlebury,Alexander J. Cowan,Mónica Barroso,Kevin Sivula,Jinhua Ye,Michaël Grätzel,David R. Klug,Junwang Tang,James R. Durrant
摘要
Photogenerated charge carrier dynamics are investigated as a function of applied bias in a variety of different hematite photoanodes for solar water oxidation. Transient absorption spectroscopy is used to probe the photogenerated holes, while transient photocurrent measures electron extraction. We report a general quantitative correlation between the population of long-lived holes and the photocurrent amplitude. The yield of long-lived holes is shown to be determined by the kinetics of electron-hole recombination. These recombination kinetics are shown to be dependent upon applied bias, exhibiting decay lifetimes ranging from ca 5 μs to 3 ms (at −0.4 and +0.4 V versus Ag/AgCl, respectively). For Si-doped nanostructured hematite photoanodes, electron extraction and electron-hole recombination are complete within ∼20 ms, while water oxidation is observed to occur on a timescale of hundreds of milliseconds to seconds. The competition between electron extraction and electron-hole recombination is electron-density-dependent: the effect on recombination of applied bias and excitation intensity is discussed. The timescale of water oxidation is independent of the concentration of photogenerated holes, indicating that the mechanism of water oxidation on hematite is via a sequence of single-hole oxidation steps.
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