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Porphyrins as Templates for Site-Selective Atomic Layer Deposition: Vapor Metalation and in Situ Monitoring of Island Growth

机译:卟啉作为位点选择性原子层沉积的模板:蒸汽金属化和原位监测岛的生长

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摘要

Examinations of enzymatic catalysts suggest one key to efficient catalytic activity is discrete size metallo clusters. Mimicking enzymatic cluster systems is synthetically challenging because conventional solution methods are prone to aggregation or require capping of the cluster, thereby limiting its catalytic activity. We introduce site-selective atomic layer deposition (ALD) on porphyrins as an alternative approach to grow isolated metal oxide islands that are spatially separated. Surface-bound tetra-acid free base porphyrins (H2TCPP) may be metalated with Mn using conventional ALD precursor exposure to induce homogeneous hydroxide synthetic handles which acts as a nucleation point for subsequent ALD MnO island growth. Analytical fitting of in situ QCM mass uptake reveals island growth to be hemispherical with a convergence radius of 1.74 nm. This growth mode is confirmed with synchrotron grazing-incidence small-angle X-ray scattering (GISAXS) measurements. Finally, we extend this approach to other ALD chemistries to demonstrate the generality of this route to discrete metallo island materials.
机译:酶催化剂的研究表明,有效催化活性的关键之一是离散尺寸的金属簇。模仿酶促簇系统在合成上具有挑战性,因为常规溶液方法易于聚集或需要对簇进行封端,从而限制了其催化活性。我们在卟啉上引入位点选择性原子层沉积(ALD),作为生长空间分隔的孤立金属氧化物岛的替代方法。可以使用常规的ALD前驱体暴露,用Mn对表面结合的四酸游离碱卟啉(H2TCPP)进行金属化,以诱导均质的氢氧化物合成柄,其充当后续ALD MnO岛生长的成核点。对原位QCM质量吸收的分析拟合显示,岛屿生长为半球形,会聚半径为1.74 nm。同步加速器掠入射小角X射线散射(GISAXS)测量证实了这种生长模式。最后,我们将该方法扩展到其他ALD化学方法,以证明该方法对离散金属岛材料的通用性。

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