MnCoGe-based compounds undergo a giant negative thermal expansion (NTE) during the martensitic structural transition from Ni2In-type hexagonal to TiNiSi-type orthorhombic structure. High-resolution neutron diffraction experiments revealed that the expansion of unit cell volume can be as large as ΔV/V ∼ 3.9%. The optimized compositions with concurrent magnetic and structural transitions have been studied for magnetocaloric effect. However, these materials have not been considered as NTE materials partially due to the limited temperature window of phase transition. The as-prepared MnCoGe-based compounds are quite brittle and naturally collapse into powders. By using a few percents (3-4%) of epoxy to bond the powders, we introduced residual stress in the bonded samples and thus realized the broadening of structural transition by utilizing the specific characteristics of lattice softening enforced by the stress. As a result, giant NTE (not only the linear NTE coefficient α but also the operation-temperature window) has been achieved. For example, the average α̅ as much as -51.5 × 10(-6)/K with an operating temperature window as wide as 210 K from 122 to 332 K has been observed in a bonded MnCo0.98Cr0.02Ge compound. Moreover, in the region between 250 and 305 K near room temperature, the α value (-119 × 10(-6)/K) remains nearly independent of temperature. Such an excellent performance exceeds that of most other materials reported previously, suggesting it can potentially be used as a NTE material, particularly for compensating the materials with large positive thermal expansions.

A dual-emissive optical sensor based on the fluorescence intensity ratio (FIR) technique has been demonstrated to have significant advantages of high sensitivity and reliability. Here, we designed and successfully prepared a selfcalibrated optical luminescent thermometer of CsPbBr 3 quantum dot (QD) encapsulated lanthanide metal−organic frameworks (Eu-BTC), and their phase compositions and luminescence properties have been characterized. Different thermo-response luminescence behaviors originating from the photoluminescence of CsPbBr 3 QDs at 528 nm and the 5 D 0 − 7 F 2 emission of Eu 3+ at 618 nm were investigated in the temperature range of 20−100 °C, in which the dual-emissive temperature-dependent emissions can serve as a ratiometric thermometer for accurate temperature monitoring applications. Significantly, the as-obtained CsPbBr 3 @ Eu-BTC hybrid exhibited a high relative sensitivity (S r ) of 3.9% °C−1 at 20 °C and excellent temperature resolution of 0.004 °C in the measured temperature range, indicating its superiority as a ratiometric luminescent thermometer for temperature sensing. The related luminescent sensing mechanism of the CsPbBr 3 @Eu-BTC is also discussed, and this work provides an effective strategy for the rational design of a reliable and stable thermometer by integrating CsPbBr 3 QDs and a carrier of a luminescent lanthanide organic framework.

A new salicylideneaniline-based organogelator has been synthesized, and it can gelatinize organic solvents, including cyclohexane, toluene, benzene, and some mixed solvents. SEM images show that it has self-assembled into 1-D nanofibers, which further cross-link to form 3-D network. On the basis of the results of small-angle XRD and the optimized molecular length by semiempirical quantum calculations, the gelators are supposed to pack into a unimolecular lamellar structure with a period of 3.01 nm. Significantly, reversible chromism is realized with respect of the tautomerism between the NH and OH forms during the sol-gel freezing repetition. Furthermore, the gel can emit intense green light, and the fluorescent quantum yield of the gel is approximately 600 times higher than that of the solution. The aggregation-induced emission enhancement is ascribed to the formation of J aggregation and the inhibition of intramolecular rotation in the gel state.

A liquid crystal with an azobenzene moiety as a photoactive mesogenic unit is investigated in photoinduced birefringence. Measurements reveal that it possesses large magnitude of photoinduced birefringence (Δn∼10−2) and the characteristic of long-term optical storage. The resulting polarization information can be erased either by heating the sample to a temperature much higher than the glass transition temperature, or by optical method with a circularly polarized light. The mechanism of long-term optical storage is discussed in this letter.

We report on the synthesis and self-assembly of a new series of discotic molecules containing triphenylbenzene as the core and alkoxy side chain with varying length. It was found that compounds 3 a-c, 4 b and 5 b could form stable gels in several apolar solvents. Transmission electron microscopy (TEM) images revealed that their morphologies were very different for the different alkoxy-substituted organogels. In toluene or hexane, 3 b and 3 c resulted in both left- and right-handed helical fibers, whereas 3 a resulted in straight rigid fibers; 4 b and 5 b resulted in most straight fibers with a few twisted fibers. The results from FT-IR and UV/Vis absorption spectroscopy indicated that the hydrogen bonding and pi-pi interactions were the main driving forces for the formation of the self-assembled gels. Further detailed analysis of their aggregation modes were conducted by UV-visible absorption spectra and X-ray diffraction (XRD) measurements. Based on these findings, the influence of these peripheral alkoxy substituents on the gel formation and the aggregation mode were discussed. The special enhanced fluorescent emissions, which resulted from aggregation, were also found in the gel phase.