Jiamprasertboon Arreerat, Kafizas Andreas, Sachs Michael, Ling Min, Alotaibi Abdullah M, Lu Yao, Siritanon Theeranun, Parkin Ivan P, Carmalt Claire J
School of Chemistry, Institute of Science, Suranaree University of Technology, 111 University Avenue, Muang, Nakhon Ratchasima, 30000, Thailand.
Material Chemistry Centre, Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK.
Chemistry. 2019 Aug 27;25(48):11337-11345. doi: 10.1002/chem.201902175. Epub 2019 Aug 1.
Type I heterojunction films of α-Fe O /ZnO are reported here as a non-titania based photocatalyst, which shows remarkable enhancement in the photocatalytic properties towards stearic acid degradation under UVA-light exposure (λ=365 nm), with a quantum efficiency of ξ=4.42±1.54×10 molecules degraded/photon, which was about 16 times greater than that of α-Fe O , and 2.5 times greater than that of ZnO. Considering that the degradation of stearic acid requires 104 electron transfers for each molecule, this represents an overall quantum efficiency of 4.60 % for the α-Fe O /ZnO heterojunction. Time-resolved transient absorption spectroscopy (TAS) revealed the charge-carrier behaviour responsible for this increase in activity. Photogenerated electrons, formed in the ZnO layer, were transferred into the α-Fe O layer on the pre-μs timescale, which reduced electron-hole recombination. This increased the lifetime of photogenerated holes formed in ZnO, which oxidise stearic acid. The heterojunction α-Fe O /ZnO films grown herein show potential environmental applications as coatings for self-cleaning windows and surfaces.
本文报道了α-Fe₂O₃/ZnO的I型异质结薄膜作为一种非二氧化钛基光催化剂,其在紫外光(λ = 365 nm)照射下对硬脂酸降解的光催化性能有显著增强,量子效率为ξ = 4.42±1.54×10⁻⁴个分子降解/光子,约为α-Fe₂O₃的16倍,ZnO的2.5倍。考虑到每个硬脂酸分子降解需要104次电子转移,这意味着α-Fe₂O₃/ZnO异质结的整体量子效率为4.60%。时间分辨瞬态吸收光谱(TAS)揭示了导致活性增加的电荷载流子行为。在ZnO层中形成的光生电子在微秒时间尺度上转移到α-Fe₂O₃层,这减少了电子-空穴复合。这增加了在ZnO中形成的氧化硬脂酸的光生空穴的寿命。本文生长的α-Fe₂O₃/ZnO异质结薄膜作为自清洁窗户和表面的涂层显示出潜在的环境应用。