Extraction of mobile charge carrier photogeneration yield spectrum of ultrathin-film metal oxide photoanodes for solar water splitting

材料科学 氧化物 金属 分解水 光电子学 产量(工程) 载流子 纳米技术 化学 光催化 生物化学 冶金 催化作用
作者
Daniel A. Grave,David S. Ellis,Yifat Piekner,Moritz Kölbach,Hen Dotan,Asaf Kay,Patrick Schnell,Roel van de Krol,Fatwa F. Abdi,Dennis Friedrich,Avner Rothschild
出处
期刊:Nature Materials [Nature Portfolio]
卷期号:20 (6): 833-840 被引量:41
标识
DOI:10.1038/s41563-021-00955-y
摘要

Light absorption in strongly correlated electron materials can excite electrons and holes into a variety of different states. Some of these excitations yield mobile charge carriers, whereas others result in localized states that cannot contribute to photocurrent. The photogeneration yield spectrum, ξ(λ), represents the wavelength-dependent ratio between the contributing absorption that ultimately generates mobile charge carriers and the overall absorption. Despite being a vital material property, it is not trivial to characterize. Here, we present an empirical method to extract ξ(λ) through optical and external quantum efficiency measurements of ultrathin films. We applied this method to haematite photoanodes for water photo-oxidation, and observed that it is self-consistent for different illumination conditions and applied potentials. We found agreement between the extracted ξ(λ) spectrum and the photoconductivity spectrum measured by time-resolved microwave conductivity. These measurements revealed that mobile charge carrier generation increases with increasing energy across haematite’s absorption spectrum. Low-energy non-contributing absorption fundamentally limits the photoconversion efficiency of haematite photoanodes and provides an upper limit to the achievable photocurrent that is substantially lower than that predicted based solely on absorption above the bandgap. We extended our analysis to TiO2 and BiVO4 photoanodes, demonstrating the broader utility of the method for determining ξ(λ). Although the photogeneration yield spectrum is a key property for photoabsorbers in photovoltaic and photoelectrochemical cells, its characterization remains challenging. An empirical method to extract this parameter through quantum efficiency measurements of ultrathin films is proposed.
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