摘要
Macroporous terbium-doped Ca 12 Al 14 O 32 Cl 2 (C12A7:Tb 3+ ) monoliths were synthesized via a sol-gel route accompanied by phase separation, and the luminescence performances and detection of Ag + in water of the C12A7:Tb 3+ monoliths were investigated in detail. The simulation of the hydrolysis and dimerization reactions of C12A7:Tb 3+ shows that the hydrolysis and dimerization of Tb 3+ are prior to Al 3+ , and the doped Tb 3+ will affect the sol-gel transition of the system. The addition of Tb element changes the macrostructure derived from phase separation and sol-gel transition, and decreases the macropore size of C12A7 monolith. Heat treatment allows the formation of a single mayenite phase C12A7:Tb 3+ without spoiling the macrostructure, and the Tb 3+ ions replace the position of the Ca 2+ ions of the “cage” structure without destroying the lattice structure of C12A7. The luminescence intensity of C12A7:3%Tb 3+ monolith reaches the maximum, and the corresponding macropore size and porosity are 0.3 μm and 79% respectively. High luminescence intensity of C12A7:Tb 3+ monolith is attributed to higher scattering light and wonderful high temperature stability derived from the macrostructure. The obtained macroporous C12A7:Tb 3+ material has a sensitive response to Ag + ions, and can become a promising fluorescence sensor for the detection of Ag + ions.
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