Visible-light-driven lanthanide-organic-frameworks modified TiO2 photocatalysts utilizing up-conversion effect

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作者
Parnicka, Patrycja [1 ]
Lisowski, Wojciech [2 ]
Klimczuk, Tomasz [3 ]
Luczak, Justyna [4 ]
Żak, Andrzej [5 ]
Zaleska-Medynska, Adriana [1 ]
机构
[1] Department of Environmental Technology, Faculty of Chemistry, University of Gdansk, Gdansk,80-308, Poland
[2] Institute of Physical Chemistry, Polish Academy of Sciences, Warsaw,01-224, Poland
[3] Faculty of Applied Physics and Mathematics, Gdansk University of Technology, Gdansk,80-233, Poland
[4] Department of Process Engineering and Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, Gdansk,80-233, Poland
[5] Electron Microscopy Laboratory, Faculty of Mechanical Engineering, Wroclaw University of Science and Technology, Wroclaw,50-372, Poland
关键词
Energy transfer - Light - Antennas - Quantum theory - Metal-Organic Frameworks - Biodegradation - Titanium dioxide - Metal ions - Photocatalytic activity - Rare earth elements - Rare earths - Ground state - Mass transfer;
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摘要
Highly efficient and quite stable composite with core-shell-like architecture reported herein, responds to the challenge of sunlight-driven photocatalysts. The Ln(ndc)/TiO2 photocatalytic system comprises active lanthanide-carboxylate coordination networks (Nd, Er, Ho, and Tm as metal ions, and 2,6-naphthalene dicarboxylic acid as the organic linker) and inert titanium dioxide and allow to convert incompatible visible radiation into functional ultraviolet photons. The combination of the antenna-reactor photocatalyst complex with Ln(ndc) shell layers promotes light harvesting and efficient mass transfer, resulting in additional photoexcited electrons. The Nd(ndc) metal-organic framework successfully activate TiO2 via up-conversion energy transfer. The apparent quantum efficiency, determined at wavelengths corresponding to the transitions from the Nd3+ ground state, equals to 2.8% and 3.2% for 525 and 583 nm, respectively. Integration of the Nd(ndc) MOF and TiO2 results in the highest efficiency of phenol degradation, affording a value of 87.5% after 60 min of visible light (λ > 420 nm) exposure. © 2021 The Authors
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