Highly Stable Self-Cleaning Paints Based on Waste-Valorized PNC-Doped TiO2 Nanoparticles

被引:13
|
作者
Maqbool, Qaisar [1 ,2 ]
Favoni, Orlando [1 ]
Wicht, Thomas [2 ]
Lasemi, Niusha [2 ]
Sabbatini, Simona [1 ]
Stoeger-Pollach, Michael [3 ]
Ruello, Maria Letizia [1 ]
Tittarelli, Francesca [1 ]
Rupprechter, Gunther [2 ]
机构
[1] Univ Politecn Marche, Dept Mat Environm Sci & Urban Planning SIMAU, INSTM Res Unit, I-60131 Ancona, Italy
[2] Inst Mat Chem, TU Wien, A-1060 Vienna, Austria
[3] TU Wien, Univ Serv Ctr Transmiss Electron Microscopy, A-1040 Vienna, Austria
基金
奥地利科学基金会;
关键词
green synthesis; waste upcycling; photocatalysis; self-cleaning paints; doped TiO2 nanoparticles; PHOTOCATALYTIC ACTIVITY; OXIDATIVE DEHYDROGENATION; INFRARED-SPECTROSCOPY; ORGANIC FRAMEWORKS; OXYGEN EVOLUTION; RUTILE; TITANIUM; ANATASE; PHOTOLUMINESCENCE; PHOSPHATES;
D O I
10.1021/acscatal.3c06203
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Adding photocatalytically active TiO2 nanoparticles (NPs) to polymeric paints is a feasible route toward self-cleaning coatings. While paint modification by TiO2-NPs may improve photoactivity, it may also cause polymer degradation and release of toxic volatile organic compounds. To counterbalance adverse effects, a synthesis method for nonmetal (P, N, and C)-doped TiO2-NPs is introduced, based purely on waste valorization. PNC-doped TiO2-NP characterization by vibrational and photoelectron spectroscopy, electron microscopy, diffraction, and thermal analysis suggests that TiO2-NPs were modified with phosphate (P & boxH;O), imine species (R & boxH;N-R), and carbon, which also hindered the anatase/rutile phase transformation, even upon 700 degrees C calcination. When added to water-based paints, PNC-doped TiO2-NPs achieved 96% removal of surface-adsorbed pollutants under natural sunlight or UV, paralleled by stability of the paint formulation, as confirmed by micro-Fourier transform infrared (FTIR) surface analysis. The origin of the photoinduced self-cleaning properties was rationalized by three-dimensional (3D) and synchronous photoluminescence spectroscopy, indicating that the dopants led to 7.3 times stronger inhibition of photoinduced e(-)/h(+) recombination when compared to a benchmark P25 photocatalyst.
引用
收藏
页码:4820 / 4834
页数:15
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