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Synthesis of ultrafine ruthenium phosphide nanoparticles and nitrogen/phosphorus dual-doped carbon hybrids as advanced electrocatalysts for all-pH hydrogen evolution reaction

机译:超细磷化钌纳米颗粒和氮/磷双掺杂碳杂化物的合成作为全pH析氢反应的高级电催化剂

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Pt-group metal phosphides are widely utilized as efficient electrocatalysts for hydrogen evolution reaction (HER), whereas most of the synthetic strategies are complicated, dangerous, and toxic with the use of large amount of nitrogen (N) and/or phosphorus (P) sources. Here, we report the synthesis of ruthenium phosphide nanoparticles (NPs) confined into N/P dual-doped carbon by pyrolyzing self-prepared ruthenium-organo-phosphine complex using 1,3,5-triaza-7-phosphadamantane (PTA) as the ligand and N/P sources. The achieved S-RuP2/NPC displayed excellent electrocatalytic activity (over-potentials of 19, 37, and 49 mV in alkaline, neutral, and acidic media, respectively, at 10 mA cm(-2)) toward HER at all pH ranges. The high performance of S-RuP2/NPC must be ascribed to the homogeneously distributed and P-rich RuP(2)NPs with the diameter of 3.29 nm on the NPC surface, which can considerably improve the atom utilization for HER. The present synthetic strategy not only avoids the use of additional N/P sources but also the generation of flammable and toxic PH3 gas. This synthetic strategy can be extended to prepare other traditional metal phosphides for electrocatalytic applications. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:铂族金属磷化物被广泛用作氢释放反应(HER)的有效电催化剂,而大多数合成策略由于使用大量氮(N)和/或磷(P)而复杂,危险且有毒资料来源。在这里,我们报告了通过使用1,3,5-triaza-7-phosphadamantane(PTA)作为热解自制备的钌-有机膦配合物,将磷化钌纳米颗粒(NPs)限制在N / P双掺杂碳中的合成。配体和N / P来源。所实现的S-RuP2 / NPC在所有pH范围内均对HER具有出色的电催化活性(在碱性,中性和酸性介质中分别在10 mA cm(-2)时过电19、37和49 mV)。 S-RuP2 / NPC的高性能必须归因于NPC表面直径为3.29 nm的均匀分布且富含P的RuP(2)NP,这可以大大提高HER的原子利用率。当前的合成策略不仅避免使用其他N / P来源,而且避免生成易燃和有毒的PH3气体。这种合成策略可以扩展,以制备用于电催化应用的其他传统金属磷化物。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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