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Luminescence Enhancement after Adding Organic Salts to Nanohybrid under Aqueous Condition

机译:在水性条件下向纳米杂化物中添加有机盐后的发光增强

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摘要

Lanthanide-based organicinorganic hybrid materials (LnOIH) are of immense importance for various applications nowadays, while it still remains a significant challenge to achieve high luminescence efficiency in aqueous environment. Herein we present a simple and environmentally friendly two-step strategy to prepare strongly red-light emitting nano-LnOIH by first in situ forming Eu3+-beta-dikeonate complexes on Laponite platelets and subsequently increasing the coordination number of the complexes via the modification with a silane-functionalized imidazolium salt, which can fully protect Eu3+ ions from the water molecule quenching. The mechanism of how the imidazolium salt favors the formation of Eu3+-beta-dikeonate complex with large coordination number was elucidated. The result is that the removal of the abundant protons on the Laponite platelets through a mechanism of synergic effect of ion exchange and neutralization drives the formation of Eu3+-beta-diketonate complexes with high coordination number. The high efficiency of the resulting luminescent nano-LnOIH in water endows the nanohybrid with good aqueous solution processability and opens the possibility of using them under complicated aqueous conditions for biorelated applications.
机译:如今,基于镧系元素的有机无机杂化材料(LnOIH)对于各种应用具有极其重要的意义,而在水性环境中实现高发光效率仍然是一项重大挑战。本文中,我们提出了一种简单且环保的两步策略,即通过首先在Laponite血小板上原位形成Eu3 +-β-二酮酸酯复合物,然后通过修饰A来增加复合物的配位数,从而制备强红色发光的纳米LnOIH。硅烷官能化的咪唑鎓盐,可以充分保护Eu3 +离子免受水分子淬灭。阐明了咪唑鎓盐如何促进具有大配位数的Eu3 +-β-二酮酸酯复合物形成的机理。结果是,通过离子交换和中和的协同作用机制,Laponite血小板上的大量质子的去除驱动了具有高配位数的Eu3 +-β-二酮酮酸酯络合物的形成。所得发光纳米LnOIH在水中的高效率赋予纳米杂化物以良好的水溶液可加工性,并为在复杂的水性条件下将其用于生物相关应用提供了可能性。

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