14 research outputs found

    Luminescent Metal–Organic Framework Thin Films: From Preparation to Biomedical Sensing Applications

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    Metal-organic framework (MOF) thin films are receiving increasing attention in a number of different application fields, such as optoelectronics, gas separation, catalysis electronic devices, and biomedicine. In particular, their tunable composition and structure, accessible metal sites and potential for post-synthetic modification for molecular recognition make MOF thin films promising candidates for biosensing applications. Compared with solution-based powdery probes, film-based probes have distinct advantages of good stability and portability, tunable shape and size, real-time detection, non-invasion, extensive suitability in gas/vapor sensing, and recycling. In this review, we summarize the recent advances in luminescent MOF thin films, including the fabrication methods and origins of luminescence. Specifically, luminescent MOF thin films as biosensors for temperature, ions, gases and biomolecules are highlighted

    Facile Preparation and Highly Efficient Catalytic Performances of Pd-Cu Bimetallic Catalyst Synthesized via Seed-Mediated Method

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    With the rapid development of industry, the problem of environmental pollution has become increasingly prominent. Exploring and preparing green, efficient, and low cost catalysts has become the key challenge for scientists. However, some conventional preparation methods are limited by conditions, such as cumbersome operation, high energy consumption, and high pollution. Here, a simple and efficient seed-mediated method was designed and proposed to synthesize a highly efficient bimetallic catalyst for catalyzing nitro compounds. A Pd-Cu bimetallic composite (BCM) can be prepared by synthesizing the original seed crystal of precious metal palladium, then growing the mature nanocrystalline palladium and supporting the transition metal copper. Importantly, after eight consecutive catalytic cycles, the conversion of the catalyzed 2-NA was 84%, while the conversion of the catalyzed 4-NP was still 72%. And the catalytic first order rates of 2-NA and 4-NP constants were 0.015 s−1, and 0.069 s−1, respectively. Therefore, current research of nanocomposites catalyst showed great significance for serious environmental pollution problems and the protection of living environment, providing a new idea for the preparation of new bimetallic catalytic materials

    Highly Efficient Catalytic Performances of Nitro Compounds and Morin via Self-Assembled MXene-Pd Nanocomposites Synthesized through Self-Reduction Strategy

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    With development of the society, the problem of environmental pollution is becoming more and more serious. There is the urgent need to develop a new type of sustainable green material for degradable pollutants. However, the conventional preparation method is limited by conditions such as cumbersome operation, high energy consumption, and high pollution. Here, a simple method named self-reduction has been proposed, to synthesize highly efficient catalytic nitro compounds and morin self-assembled MXene-Pd nanocomposites. Palladium nanoparticles were grown in situ on MXene nanosheets to form MXene@PdNPs. MXene@PdNPs composites with different reaction times were prepared by adjusting the reduction reaction time. In particular, MXene@PdNPs20 exhibited a high catalytic effect on 4-NP and 2-NA, and the first-order rate constants of the catalysis were 0.180 s−1 and 0.089 s−1, respectively. It should be noted that after eight consecutive catalytic cycles, the conversion to catalyze 4-NP was still greater than 94%, and the conversion to catalyze 2-NA was still greater than 91.8%. Therefore, the research of self-assembled MXene@PdNPs nanocomposites has important potential value for environmental management and sustainable development of human health, and provides new clues for the future research of MXene-based new catalyst materials

    Highly Sensitive Adsorption and Detection of Iodide in Aqueous Solution by a Post-Synthesized Zirconium-Organic Framework

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    Effective methods of detection and removal of iodide ions (I−) from radioactive wastewater are urgently needed and developing them remains a great challenge. In this work, an Ag+ decorated stable nano-MOF UiO-66-(COOH)2 was developed for the I− to simultaneously capture and sense in aqueous solution. Due to the uncoordinated carboxylate groups on the UiO-66-(COOH)2 framework, Ag+ was successfully incorporated into the MOF and enhanced the intrinsic fluorescence of MOF. After adding iodide ions, Ag+ would be produced, following the formation of AgI. As a result, Ag+@UiO-66-(COOH)2 can be utilized for the removal of I− in aqueous solution, even in the presence of other common ionic ions (NO2−, NO3−, F−, SO42−). The removal capacity as high as 235.5 mg/g was calculated by Langmuir model; moreover, the fluorescence of Ag+@UiO-66-(COOH)2 gradually decreases with the deposition of AgI, which can be quantitatively depicted by a linear equation. The limit of detection toward I− is calculated to be 0.58 ppm

    OsWRKY67 positively regulates blast and bacteria blight resistance by direct activation of PR genes in rice

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    Abstract Background WRKY proteins are one of the largest gene families and are well-known for their regulatory roles in many aspects of plant development, including plant response to both biotic and abiotic stresses. Although the roles of WRKY proteins in leaf blast resistance have been well-documented in rice, their functions in panicle blast, the most destructive type of blast disease, are still largely unknown. Results Here, we identified that the transcription of OsWRKY67 was strongly activated by leaf and panicle blast infection. OsWRKY67 is ubiquitously expressed and sub-localized in the nucleus. Rice plants overexpressing OsWRKY67 showed quantitatively enhanced resistance to leaf blast, panicle blast and bacterial blight. In contrast, silencing of OsWRKY67 increased the susceptibility to blast and bacterial blight diseases. RNA-seq analysis indicated that OsWRKY67 induces the transcription of a set of defense-related genes including the ones involved in the salicylic acid (SA)-dependent pathway. Consistent with this, the OsWRKY67-overexpressing plants accumulated higher amounts of endogenous SA, whereas lower endogenous SA levels were observed in OsWRKY67-silenced plants relative to wild-type Nipponbare plants before and after pathogen attack. Moreover, we also observed that OsWRKY67 directly binds to the promoters of PR1a and PR10 to activate their expression. Conclusions These results together suggest the positive role of OsWRKY67 in regulating rice responses to leaf blast, panicle blast and bacterial blight disease. Furthermore, conferring resistance to two major diseases makes it a good target of molecular breeding for crop improvement in rice

    Turn-on and Ratiometric Luminescent Sensing of Hydrogen Sulfide Based on Metal–Organic Frameworks

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    The sensing of hydrogen sulfide (H<sub>2</sub>S) has become a long-time challenging task. In this work, we developed a general strategy for sensing of H<sub>2</sub>S utilizing postsynthetic modification of a nano metal–organic frameworks (MOF) UiO-66-(COOH)<sub>2</sub> with Eu<sup>3+</sup> and Cu<sup>2+</sup> ions. The nano MOF Eu<sup>3+</sup>/Cu<sup>2+</sup>@UiO-66-(COOH)<sub>2</sub> displays the characteristic Eu<sup>3+</sup> sharp emissions and the broad ligand-centered (LC) emission simultaneously. Because H<sub>2</sub>S can strongly increase the fluorescence of Eu<sup>3+</sup> and quench the broad LC emission through its superior affinity for Cu<sup>2+</sup> ions, the MOF Eu<sup>3+</sup>/Cu<sup>2+</sup>@UiO-66-(COOH)<sub>2</sub> exhibits highly sensitive turn-on sensing of H<sub>2</sub>S over other environmentally and biologically relevant species under physiological conditions. Furthermore, this approach for fluorescent turn-on sensing of H<sub>2</sub>S is expected to extend to other water-stable MOFs containing uncoordinated −COOH
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