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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Emerging metal ion-coordinated black phosphorus nanosheets and black phosphorus quantum dots with excellent stabilities
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Emerging metal ion-coordinated black phosphorus nanosheets and black phosphorus quantum dots with excellent stabilities

机译:新兴金属离子协调的黑色磷纳米片和黑色磷量子点,具有优异的稳定性

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In this work, emerging metal ion-coordinated black phosphorus nanosheets (M@BPNSs) and quantum dots (M@BPQDs) were prepared via the sonication-assisted liquid-phase exfoliation of bulk black phosphorus (BP) crystals in the presence of a metal ion (M) and solvothermal reaction of the exfoliated few-layer M@BP nanosheets. Based on theoretical calculations, a bonding mode exists between M and BP. Consequently, the adsorption energies of M on BP via the bonding mode are lower than that of M on BP via the non- bonding mode. Under the bonding mode, the adsorption energy of Zn2+ (-2.04 eV) on BP is lower than other M. Zn2+, serves as the preferred M and can be easily adsorbed on the surface of BP. We experimentally prepared emerging M@BPNSs and M@BPQDs, characterized, and compared various morphologies, microstructures and spectra under different conditions. It is verified, that the surface coordination of M with BP protects BP from oxidization and degradation of its nanostructures upon exposure to O-2 and H2O. In comparison to the bare BPNSs, Zn@BPNSs showed high microstructural stability. Moreover, in comparison to bare BPQDs, Zn@BPQDs exhibited high colloidal stability and excellent stabilities with fluorescence and photothermal conversion performances. The long-term stabilities are due to the M-coordination with BP through P-M bonding on BP nanostructures. Thus, the excellent long-term stabilities in microstructure, fluorescence and photothermal conversion levels endow the emerging two-dimensional M@BPNSs and zero-dimensional M@BPQDs with great prospects towards promising applications, especially in electronics, optoelectronics, optical and biomedical fields.
机译:在这项工作中,通过在金属存在下,通过散装黑磷(BP)晶体的超声辅助液相剥离来制备新出现的金属离子协调的黑色磷纳米片(M @ BPNS)和量子点(M @ BPQDS)剥落的少数层M @ BP纳米片的离子(m)和溶剂热反应。基于理论计算,在M和BP之间存在键合模式。因此,M通过粘合模式的M对BP的吸附能量低于通过非键合模式的M on BP上的M。在粘合模式下,BP上的Zn2 +(-2.04eV)的吸附能量低于其他M. Zn2 +,作为优选的M,并且可以容易地吸附在BP的表面上。我们通过在不同条件下专用制备新兴的M @ BPNS和M @ BPQDS和M @ BPQDS,并比较各种形态,微观结构和光谱。验证,在暴露于O-2和H2O时,M与BP的表面配位免受其纳米结构的氧化和降解的氧化和降解。与裸BPNS相比,Zn @ BPNS显示出高的微观结构稳定性。此外,与裸BPQDS相比,Zn @ BPQDS表现出高胶体稳定性和具有优异的荧光和光热转化性能的稳定性。长期稳定性是由于BP纳米结构上通过P-M键合的M-与BP键合。因此,具有微观结构,荧光和光热转换水平的优异长期稳定性赋予了新兴的二维M @ BPNS和零维M @ BPQD,其前景迈向有前景,特别是在电子,光电子,光学和生物医学领域。

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