“…Thus, LaMOF gets a blue emission with CIE chromatic coordinates equal to (0.1836, 0.1259) (Figure S19). Compared to the emission of the pure ligand (Figure S5 in reference 23), [28] a small red‐shift is observed for the coordinated ligand, which may result from a slight change in intra‐ and inter‐molecular interactions between ligands [15] …”
Section: Resultsmentioning
confidence: 93%
“…In this context, we focus our attention on an inexpensive commercially available organic ligand, namely 1,3-benzenedicarboxylic acid, or isophthalic acid, and water as solvent. This common linker is a rigid carboxylate ligand which enables various coordination modes to build MOF network, [27][28][29][30][31] and which gets an appropriate triplet excited-state energy (27900 cm À 1 ). [32] Herein, we report the synthesis of two new isomorphous 3D lanthanide-bearing metal-organic frameworks built up from isophthalate (1,3-BDC), with the chemical composition Ln 1.14 Na 0.57 (BDC) 2 (H 2 O) • 4H 2 O (Ln=La 3 + or Ce 3 + ).…”
Two novel lanthanide metal-organic frameworks (LnMOFs), Ln 1.14 Na 0.57 (BDC) 2 (H 2 O) • 4H 2 O (Ln=La 3 + or Ce 3 + , BDC : 1,3-benzenedicarboxylate), have been synthesized under hydrothermal conditions by using a Ln 3 + coordination polymer as precursor. The crystal structure was determined from single crystal X-ray diffraction. Both compounds are isostructural and contain chains of face-sharing [LnO 10 ] polyhedra connected by the linkers to form an anionic three-dimensional network, defining both polar and apolar channels, the latter being occupied by water molecules and Ln 3 + and Na + cations. When doped by optimized content of Eu 3 + and Tb 3 + , the La 3 + counterpart exhibits white luminescence emission with CIE parameters equal to (0.3440, 0.3735) at λ exc = 321 nm, which renders the material attractive for white LED application.
“…Thus, LaMOF gets a blue emission with CIE chromatic coordinates equal to (0.1836, 0.1259) (Figure S19). Compared to the emission of the pure ligand (Figure S5 in reference 23), [28] a small red‐shift is observed for the coordinated ligand, which may result from a slight change in intra‐ and inter‐molecular interactions between ligands [15] …”
Section: Resultsmentioning
confidence: 93%
“…In this context, we focus our attention on an inexpensive commercially available organic ligand, namely 1,3-benzenedicarboxylic acid, or isophthalic acid, and water as solvent. This common linker is a rigid carboxylate ligand which enables various coordination modes to build MOF network, [27][28][29][30][31] and which gets an appropriate triplet excited-state energy (27900 cm À 1 ). [32] Herein, we report the synthesis of two new isomorphous 3D lanthanide-bearing metal-organic frameworks built up from isophthalate (1,3-BDC), with the chemical composition Ln 1.14 Na 0.57 (BDC) 2 (H 2 O) • 4H 2 O (Ln=La 3 + or Ce 3 + ).…”
Two novel lanthanide metal-organic frameworks (LnMOFs), Ln 1.14 Na 0.57 (BDC) 2 (H 2 O) • 4H 2 O (Ln=La 3 + or Ce 3 + , BDC : 1,3-benzenedicarboxylate), have been synthesized under hydrothermal conditions by using a Ln 3 + coordination polymer as precursor. The crystal structure was determined from single crystal X-ray diffraction. Both compounds are isostructural and contain chains of face-sharing [LnO 10 ] polyhedra connected by the linkers to form an anionic three-dimensional network, defining both polar and apolar channels, the latter being occupied by water molecules and Ln 3 + and Na + cations. When doped by optimized content of Eu 3 + and Tb 3 + , the La 3 + counterpart exhibits white luminescence emission with CIE parameters equal to (0.3440, 0.3735) at λ exc = 321 nm, which renders the material attractive for white LED application.
“…From the application point of view, these thermometers stand out due to the broad range of temperatures in which they have been demonstrated to perform. Indeed, there are few examples of compositions that present high sensitivities (between 1 %K -1 and 10 %K -1 ) in the cryogenic range, and thus are proposed for applications dealing with them, as might be the case in aerospace industry or regarding superconducting magnets, to cite some [111][112][113].…”
Temperature is a basic parameter influencing the behavior of systems in physics, chemistry and biology. From living cells to microcircuits, a wide range of cases require thermometry techniques that can be applied to reduced areas, offering sub-micrometric resolution and high accuracy. Since traditional thermometers cannot be applied in such systems, alternative tools have been specifically designed to measure temperature at the nanoscale; including scanning thermal microscopy, non-contact optical techniques or various types of luminescent nanoparticles. Each option presents interesting advantages, but also limitations that need to be considered and understood. We provide here an overview of the main currently available nanothermometry tools, discussing their pros and cons toward potential applications.
“…Recently, we investigated the thermometric properties of an Eu–Tb mixed MOF built upon the bidentate linker 1,3‐benzene‐dicarboxylic acid (1,3‐H 2 bdc, also called isophthalic acid), namely [Tb 0.87 Eu 0.13 (1,3‐bdc) 3 (H 2 O) 2 ], presenting the maximum relative thermal sensitivity in the cryogenic range ( T < 100 K). [ 23 ] The 1,3‐H 2 bdc linker is a bidentate ligand with different geometric effects to connect metal ions into multidimensional structures via numerous coordination modes. Consequently, several MOFs based on this ligand have been already reported with different structuration, despite their thermometric performance has not always been studied.…”
In the last decade, numerous Ln‐bearing metal‐organic frameworks (MOFs) have been reported for luminescence thermometry applications. Although the Ln3+ composition is always thoroughly determined, this parameter is never optimized to improve thermometric performances. Here, the optimization of thermometric performances of luminescent probes is tackled by reporting a series of mixed Eu3+–Tb3+ metal‐organic frameworks. The thermometric performances are accessed as a function of the Eu3+ content yielding a maximum relative sensitivity between 0.19 and 0.44% K−1 registered at temperatures between 340 and 240 K, respectively. A meticulous theoretical investigation of the Tb3+‐to‐Eu3+ energy transfer in the series of mixed Eu3+–Tb3+ MOFs is also performed to determine the predominant pathway of the energy transfer. For the first time, a clear evidence of the significant influence of the Eu/Tb ratio on the energy transfer between Ln3+ emitting centers is presented that definitively determines the operating temperature range and the maximum relative sensitivity of the luminescent thermal probes.
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