RESUMO
In light of the escalating industrial and environmental pollution, there is a pressing need for the development of novel materials capable of swiftly detecting pollutants. Here, we report the synthesis of five lanthanide metal-organic frameworks sharing a common structure, prepared via a hydrothermal method and denoted as [Ln2(H2DHBDC)2(phen)(H2O)6]n (where CUST-888 corresponds to Tb, CUST-889 corresponds to Eu, CUST-890 corresponds to Gd, CUST-891 corresponds to Dy, and CUST-892 corresponds to Nd). Notably, CUST-888 and CUST-889 exhibit discernible visual alterations in response to acidic and alkaline conditions. To assess their practical utility, luminescent test strips and light-emitting diode lights based on CUST-888 and CUST-889 were devised, enabling the visual detection of luminescence color changes induced by Hg2+, Cr2O72-, tetracycline, and 2,4,6-trinitrophenol. Furthermore, highlighters derived from CUST-888 and CUST-889 were designed, showcasing robust stability, adjustable color, and substantial potential for application in the realm of anticounterfeiting.
RESUMO
The design and development of efficient and durable catalysts with visible-light response for photocatalytic hydrogen production and pollutants degradation is considered as one of the most challenging tasks. In present work, a novel Cu2WS4/NiTiO3 (abbreviated as × CWS/NTO; x = 0.25, 0.50, 0.75 and 1.00) composite was prepared via a facile electrospinning/calcination technique along with a convenient hydrothermal method. The as-prepared CWS/NTOcomposite was composed of 2D CWS nanosheets and 1D NTO nanofibers manifested by SEM and TEM images. The results of XPS verified the interfacial interaction between CWS and NTO, confirming the heterojunction formation in CWS/NTOcomposite. Photocatalytic tests demonstrated as-prepared CWS/NTO catalysts exhibited outstanding and stable photocatalytic performances for H2 production and pollutants degradation under visible light (λ > 420 nm) irradiation. Specially, 0.50 CWS/NTO sample displayed the highest H2-evolution activity of 810 µmol·g-1·h-1 with the apparent quantum efficiency (AQE) value of 1.65 % at 420 nm. Additionally, it also exhibited the optimal photodegradation properties with the rate constants of 0.030, 0.413 and 0.028 min-1 for TC, RhB and Cr(VI), respectively. The excellent catalytic activities could be attributed to the enhanced visible-light adsorption, high specific surface area and efficient separation of photogenerated charge carriers. The ESR tests and free radicals capturing experiments confirmed that ·O2- and h+ were primary active species for TC/RhB degradation. Eventually, the probable catalytic mechanism was put forward and detailly analysed. The present work provides perspectives of rational design on NiTiO3-based catalysts with superior photocatalytic performance for energy regeneration and environmental remediation.