材料科学
薄膜
化学工程
分解水
光电化学电池
光电化学
氟
无机化学
电解质
光催化
催化作用
纳米技术
电极
电化学
光电子学
化学
有机化学
工程类
物理化学
冶金
作者
Martin Rohloff,Björn Anke,Olga Kasian,Qian Zhang,Martin Lerch,Christina Scheu,Anna Fischer
标识
DOI:10.1021/acsami.8b16617
摘要
Anion substitution is an emerging strategy to enhance the photoelectrochemical performance of metal oxide photoelectrodes. In the present work, we investigate the effect of fluorine incorporation on the photoelectrochemical water oxidation performance of BiVO4 and Mo:BiVO4 thin film photoanodes. The BiVO4 and Mo:BiVO4 thin film photoanodes were prepared by a straightforward organometallic solution route involving dip coating and subsequent calcination in air. Fluorine modification was realized by applying a soft and low-cost solid-vapor reaction route involving fluorine-containing polymers and an inert gas atmosphere leading to novel F:BiVO4 and F/Mo:BiVO4 thin film photoanodes with substantially increased photoelectrochemical water oxidation properties. Deposition of the cobalt phosphate (CoPi) water oxidation catalyst allowed further enhancement of the photoelectrochemical performance. While Mo doping mainly improves light-harvesting, charge transport, and charge separation efficiencies, F modification was demonstrated to primarily affect the charge transfer efficiency at the semiconductor-electrolyte interface, thereby leading to a photocurrent increase of 40 and 21% upon fluorination of the BiVO4 and Mo:BiVO4 photoanodes, respectively, and an applied bias photon-to-current efficiency increase of 35 and 5%, respectively. We thereby could demonstrate that cation and anion co-doping in BiVO4 as demonstrated for Mo and F allows combining the photoelectrochemically relevant benefits associated with each type of dopant.
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