@article {Pylarinou2021,
	title = {Visible light trapping against charge recombination in feox{\textendash}tio2 photonic crystal photocatalysts},
	journal = {Materials},
	volume = {14},
	number = {23},
	year = {2021},
	note = {cited By 0},
	abstract = {Tailoring metal oxide photocatalysts in the form of heterostructured photonic crystals has spurred particular interest as an advanced route to simultaneously improve harnessing of solar light and charge separation relying on the combined effect of light trapping by macroporous periodic structures and compositional materials{\textquoteright} modifications. In this work, surface deposition of FeOx nanoclusters on TiO2 photonic crystals is investigated to explore the interplay of slow-photon amplification, visible light absorption, and charge separation in FeOx{\textendash}TiO2 photocatalytic films. Photonic bandgap engineered TiO2 inverse opals deposited by the convective evaporation-induced coassembly method were surface modified by successive chemisorption-calcination cycles using Fe(III) acetylacetonate, which allowed the controlled variation of FeOx loading on the photonic films. Low amounts of FeOx nanoclusters on the TiO2 inverse opals resulted in diameter-selective improvements of photocatalytic performance on salicylic acid degradation and photocurrent density under visible light, surpassing similarly modified P25 films. The observed enhancement was related to the combination of optimal light trapping and charge separation induced by the FeOx{\textendash}TiO2 interfacial coupling. However, an increase of the FeOx loading resulted in severe performance deterioration, particularly prominent under UV-Vis light, attributed to persistent surface recombination via diverse defect d-states. {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.},
	doi = {10.3390/ma14237117},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-85120069672\&doi=10.3390\%2fma14237117\&partnerID=40\&md5=2ba7adfa13577866477a4da8cc09416d},
	author = {Pylarinou, M. and A. Toumazatou and E. Sakellis and Xenogiannopoulou, E. and Gardelis, S. and N. Boukos and Dimoulas, A. and V. Likodimos}
}
