4.6 Article

Atom-by-Atom Synthesis of Multiatom-Supported Catalytic Clusters by Liquid-Phase Atomic Layer Deposition

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 10, 期 11, 页码 3455-3465

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.1c07056

关键词

Atomic layer deposition; Surface organometallic chemistry; Single-site catalyst; Rational catalyst design; Supported clusters

资金

  1. European Research Council (ERC) under the European Union [758653]
  2. EPFL
  3. European Research Council (ERC) [758653] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

This paper presents a method for synthesizing atomically precise, supported multiatom catalysts using liquid-phase atomic layer deposition. The technique involves consecutive grafting reactions under mild conditions to build supported active sites atom by atom. The controlled synthesis process allows for the growth of well-defined multinuclear clusters, which were verified and characterized using various methods. Propane dehydrogenation was used as a probe reaction to demonstrate the potential of controlling and tailoring the activity and stability of these catalytic clusters.
Here, we introduce a method for the synthesis of atomically precise, supported, multiatom catalysts by liquid-phase atomic layer deposition. This technique is based on consecutive grafting reactions in mild conditions that build supported active sites atom by atom. The atomically controlled synthesis procedure led to the growth of well-defined multinuclear (Al, Mg, Si, Zn, and O) clusters. The composition of the clusters was verified by titrations ICP-OES, STEM-EDX, and XPS, while their structure was resolved from the synthesis sequence, elemental composition, and extensive characterization (X-ray absorption, solid-state NMR, STEM, XPS, and DFT calculations). Propane dehydrogenation was used as a probe reaction to demonstrate the potential to control and tailor the activity and stability of these catalytic clusters. Notably, we were able to alternatively multiply the initial activity of a known single-atom catalyst by 6 fold or improve its stability against thermal deactivation by simply using different elements and modifying the deposition sequence.

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