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Ruthenium coordinated with triphenylphosphine-hyper-crosslinked polymer: An efficient catalyst for hydrogen evolution reaction and hydrolysis of ammonia borane

机译:钌与三苯基膦-超交联聚合物配合使用:一种高效的产氢反应和氨硼烷水解的催化剂

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摘要

By using hyper-crosslinked polymer with triphenylphosphine skeleton (HCP-PPh3) as a matrix, we successfully synthesized an efficient HCP-PPh3-Ru(III) precursor for hydrogen evolution reaction (HER) and ammonia borane (AB) hydrolysis. The generated HCP-PPh3-Ru with a Ru loading of 5.0 wt% displays a high electrochemical performance for HER with an overpotential of 61 mV at a current density of 10 mA cm(-2). Moreover, HCP-PPh3-Ru with a Ru loading of 3.5 wt% exhibits the best catalytic activity for AB hydrolysis with a turnover frequency of 402 mol H-2 (mol(RU) min)(-1). The high catalytic property of the achieved catalyst is probably attributed to the substantial porosity and individual pore structure of support Furthermore, the P-functional groups in HCP-PPh3 can facilitate the anchoring of Ru functioning as coordination sites to stabilize the small Ru nanoparticles, thereby deduces the high catalytic activity. The present work provides a facile strategy for synthesizing efficient microporous organic polymer stabilized Ru catalyst for HER and aqueous AB decomposition.
机译:通过使用具有三苯基膦骨架的超交联聚合物(HCP-PPh3)作为基质,我们成功地合成了一种有效的HCP-PPh3-Ru(III)前驱体,用于氢释放反应(HER)和氨硼烷(AB)水解。生成的HCP-PPh3-Ru的Ru负载为5.0 wt%,在10 mA cm(-2)的电流密度下,超电势为61 mV的HER具有较高的电化学性能。此外,Ru负载量为3.5 wt%的HCP-PPh3-Ru对AB水解表现出最佳的催化活性,周转频率为402 mol H-2(mol(RU)min)(-1)。所获得的催化剂的高催化性能可能归因于载体的大量孔隙率和单独的孔结构。此外,HCP-PPh3中的P-官能团可以促进Ru的锚定,作为稳定小Ru纳米颗粒的配位点,从而导致高催化活性。本工作为合成用于HER和AB水溶液分解的有效的微孔有机聚合物稳定的Ru催化剂提供了一种简便的策略。

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