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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO₃ for Solar Water Oxidation.

ABSTRACT: Heterogeneous catalysts with atomically defined active centers hold great promise for high-performance applications. Among them, catalysts featuring active moieties with more than one metal atom are important for chemical reactions that require synergistic effects but are rarer than single atom catalysts (SACs). The difficulty in synthesizing such catalysts has been a key challenge. Recent progress in preparing dinuclear heterogeneous catalysts (DHCs) from homogeneous molecular precursors has provided an effective route to address this challenge. Nevertheless, only side-on bound DHCs, where both metal atoms are affixed to the supporting substrate, have been reported. The competing end-on binding mode, where only one metal atom is attached to the substrate and the other metal atom is dangling, has been missing. Here, we report the first observation that end-on binding is indeed possible for Ir DHCs supported on WO₃. Unambiguous evidence supporting the binding mode was obtained by in situ diffuse reflectance infrared Fourier transform spectroscopy and high-angle annular dark-field scanning transmission electron microscopy. Density functional theory calculations provide additional support for the binding mode, as well as insights into how end-on bound DHCs may be beneficial for solar water oxidation reactions. The results have important implications for future studies of highly effective heterogeneous catalysts for complex chemical reactions.

SUBMITTER: Zhao Y

PROVIDER: S-EPMC6161057 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO<sub>3</sub> for Solar Water Oxidation.

Zhao Yanyan Y Yan Xingxu X Yang Ke R KR Cao Sufeng S Dong Qi Q Thorne James E JE Materna Kelly L KL Zhu Shasha S Pan Xiaoqing X Flytzani-Stephanopoulos Maria M Brudvig Gary W GW Batista Victor S VS Wang Dunwei D

ACS central science 20180725 9

Heterogeneous catalysts with atomically defined active centers hold great promise for high-performance applications. Among them, catalysts featuring active moieties with more than one metal atom are important for chemical reactions that require synergistic effects but are rarer than single atom catalysts (SACs). The difficulty in synthesizing such catalysts has been a key challenge. Recent progress in preparing dinuclear heterogeneous catalysts (DHCs) from homogeneous molecular precursors has pr ...[more]

PMID: 30276249

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Project description:Layered double hydroxides (LDHs) are an ideal platform to host catalytic metal centers for water oxidation (WO) owing to the high accessibility of water to the interlayer region, which makes all centers potentially reachable and activated. Herein, we report the syntheses of three iridium-doped zinc-aluminum LDHs (Ir-LDHs) nanomaterials (1-3, with about 80 nm of planar size and a thickness of 8 nm as derived by field emission scanning electron microscopy and powder X-ray diffraction studies, respectively), carried out in the confined aqueous environment of reverse micelles, through a very simple and versatile procedure. These materials exhibit excellent catalytic performances in WO driven by NaIO4 at neutral pH and 25 °C, with an iridium content as low as 0.5 mol % (∼0.8 wt %), leading to quantitative oxygen yields (based on utilized NaIO4, turnover number up to ∼10,000). Nanomaterials 1-3 display the highest ever reported turnover frequency values (up to 402 min-1) for any heterogeneous and heterogenized catalyst, comparable only to those of the most efficient molecular iridium catalysts, tested under similar reaction conditions. The boost in activity can be traced to the increased surface area and pore volume (>5 times and 1 order of magnitude, respectively, higher than those of micrometric materials of size 0.3-1 μm) estimated for the nanosized particles, which guarantee higher noble metal accessibility. X-ray absorption spectroscopy (XAS) studies suggest that 1-3 nanomaterials, as-prepared and after catalysis, contain a mixture of isolated, single octahedral Ir(III) sites, with no evidence of Ir-Ir scattering from second-nearest neighbors, excluding the presence of IrO2 nanoparticles. The combination of the results obtained from XAS, elemental analysis, and ionic chromatography strongly suggests that iridium is embedded in the brucite-like structure of LDHs, having four hydroxyls and two chlorides as first neighbors. These results demonstrate that nanometric LDHs can be successfully exploited to engineer efficient WOCs, minimizing the amount of iridium used, consistent with the principle of the noble-metal atom economy.

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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO₃ for Solar Water Oxidation.

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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO<sub>3</sub> for Solar Water Oxidation.

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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO3 for Solar Water Oxidation.

Publications

End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO<sub>3</sub> for Solar Water Oxidation.

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OmicsDI is part of the ELIXIR infrastructure

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End-On Bound Iridium Dinuclear Heterogeneous Catalysts on WO₃ for Solar Water Oxidation.