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Concurrent Anchoring of Au NPs and Amine Groups under the Decomposition of supported L-arginine-Au(III) Complexes:A Simple Way to Active Au/C Catalyst for Pure Hydrogen Production

机译:Concurrent Anchoring of Au NPs and Amine Groups under the Decomposition of supported L-arginine-Au(III) Complexes:A Simple Way to Active Au/C Catalyst for Pure Hydrogen Production

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摘要

We propose a simple way to synthesize gold catalysts consisting of dominant ca. 2 nm nanoparticles and single atoms on different carbons by the use of L-arginine-Au(III) complexes. The decomposition of the precursor proceeds via concurrent anchoring surface amine groups and forming gold species. The gold catalyst supported on a commercial nitrogen free carbon of the Sibunit family showed excellent activity in the gas phase formic acid decomposition reaction and 100% selectivity towards hydrogen formation as compared to gold catalysts supported on nitrogen free and nitrogen doped carbon nanofibers and nanotubes. The observed increase in the reaction rate by a factor of up to 15 is due to the enrichment of external Sibunit surface with gold and surface amine groups. The intrinsic nitrogen centers of the nitrogen doped carbons are not sensitive to the gold precursor, thus not affecting the dispersion of gold and even deteriorating the catalyst activity.
机译:我们提出一个简单的方法合成金催化剂组成的主导ca。2海里纳米颗粒和单个原子在不同碳原子通过使用L-arginine-Au (3)复合物。通过并发锚定表面胺收益组织和形成黄金的物种。氮催化剂支持商业自由碳Sibunit家族的优秀活动在气相甲酸分解反应,选择性100%对氢形成比黄金催化剂支持自由和氮氮掺杂碳纳米纤维和碳纳米管。观察到的反应速率的增加15倍的浓缩外部Sibunit表面用金和表面胺组。氮掺杂碳不敏感黄金的前兆,因此没有影响分散的黄金,甚至恶化催化剂活性。

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