ABSTRACT
The high-performance optical thermometer probes are of great significance in diverse areas; lanthanide metal-organic frameworks (Ln-MOFs) are a promising candidate for luminescence temperature sensing owing to their unique luminescence properties. However, Ln-MOFs have poor maneuverability and stability in complex environments due to the crystallization properties, which then hinder their application scope. In this work, the Tb-MOFs@TGIC composite was successfully prepared using simple covalent crosslinking through uncoordinated -NH2 or COOH on Tb-MOFs reacting with the epoxy groups on TGIC {Tb-MOFs = [Tb2(atpt)3(phen)2(H2O)]n; H2atpt = 2-aminoterephthalic acid; phen = 1,10-phenanthroline monohydrate}. After curing, the fluorescence properties, quantum yield, lifetime, and thermal stability of Tb-MOFs@TGIC were remarkably enhanced. Meanwhile, the obtained Tb-MOFs@TGIC composites exhibit excellent temperature sensing properties in the low-temperature (Sr = 6.17% K-1 at 237 K), physiological temperature (Sr = 4.86% K-1 at 323 K), or high-temperature range (Sr = 3.88% K-1 at 393 K) with high sensitivity. In the temperature sensing process, the sensing mode of single emission changed into double emission for ratiometric thermometry owing to the back energy transfer (BenT) from Tb-MOFs to TGIC linkers, and the BenT process enhanced with the increase of temperature, which further improved the accuracy and sensitivity of temperature sensing. Most notably, the temperature-sensing Tb-MOFs@TGIC can be easily coated on the surface of polyimide (PI), glass plate, silicon pellet (SI), and poly(tetrafluoroethylene) plate (PTFE) substrates by a simple spraying method, which also exhibited an excellent sensing property, making it applicable for a wider T range measurement. This is the first example of a postsynthetic Ln-MOF hybrid thermometer operative over a wide temperature range including the physiological and high temperature based on back energy transfer.
ABSTRACT
Post-synthetic modification of metal-organic frameworks (MOFs) and fabrication of hybrid composites are currently hot topics in the development of new functional materials. In this study, a facile and direct approach for coupling of lanthanide MOFs with epoxy silanes was developed, providing an access to a new series of functional composites. Two types of commercially available epoxy silane, namely 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECTMS) and (3-glycidoxypropyl)methyl diethoxysilane (KH563), were used to modify Ln-BTB MOFs ([Ln(BTB)(H2O)]n·2n(C6H12O); Ln = Tb or Eu0.001Tb0.999; H3BTB = 1,3,5-benzenetrisbenzoic acid) via covalent grafting involving mechanical grinding, epoxide coupling and curing reactions. The fabricated composites (Tb-BTB@ECTMS, Eu0.001Tb0.999-BTB@ECTMS, Tb-BTB@KH563, Eu0.001Tb0.999-BTB@KH563) and their Ln-MOF precursors were fully characterized, including a detailed study of their stability and fluorescence properties. The obtained composites show high thermal and solution stability, under boiling water conditions and in a wide pH range of 1-12. Application of the composites as temperature sensors in the 197-297 K and 273-343 K temperature ranges was explored in detail, revealing a remarkable sensing behavior. For example, Tb-BTB@ECTMS shows a maximum relative sensitivity (Sr) of 6.85% K-1 at 343 K. Eu0.001Tb0.999-BTB@ECTMS represents a white-light emission material with the CIE coordinates (0.3194, 0.3049) that are very close to those of white light, along with good temperature sensing performance and a relative sensitivity of 4.32% K-1 at 297 K. An enhanced performance of the composites in comparison with the parent MOF materials as well as the mechanism of energy transfer were rationalized by DFT calculations. By unveiling a facile and efficient method for improving the stability of luminescent MOFs, via post-synthetic grafting with epoxy silanes, the present study will stimulate further research at the interface of materials chemistry, MOF design, photoluminescence and temperature sensing.
