Abstract
Fabrication of broad-spectrum response photocatalysts in a controllable manner that can efficiently utilize solar light as much as possible remains a top priority target yet a challenging task. In this work, a facile approach of synchronous bottom-up growth was employed to construct UCNP/NMIL(Ti) nanohybrids via NH2-BDC (NH2-MIL-125-ligand) linkage between upconversion NaYbF4:Tm3+ nanoparticles (~13-nm) and NH2-MIL-125. The ligand sharing integration strategy generated abundant oxygen vacancies and coordinatively-unsaturated-metal sites, efficiently enhanced light absorption, energy-transfer upconversion (UC-PL), photo-induced e-/h+ generation, and their separation (CV, EIS, Photocurrent-density). Consequently, UCNP/NMIL(Ti) exhibited excellent acetaldehyde photodegradation activity, with 12.5–77.0-folds higher rate constants (ka) than those of state-of-the-art photocatalysts under visible light and high humidity. Furthermore, the photocatalytic activity of UCNP/NMIL(Ti) only declined from 96.0% to 92.5% after five cycling-runs, demonstrating its remarkable photo-catalytic stability. Considering these attributes, the current strategy provides an avenue to synthesize efficient UCNPs/MOF composites for widespread usage in a variety of commercial applications.
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