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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Precious-metal-free Co-Fe-O-x coupled nitrogenen-riched porous carbon nanosheets derived from Schiff-base porous polymers as superior electrocatalysts for the oxygen evolution reaction
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Precious-metal-free Co-Fe-O-x coupled nitrogenen-riched porous carbon nanosheets derived from Schiff-base porous polymers as superior electrocatalysts for the oxygen evolution reaction

机译:不含希夫基多孔聚合物的无贵金属的Co-Fe-O-x偶联富氮多孔碳纳米片,是氧释放反应的优良电催化剂

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摘要

Water splitting provides a potential path for producing clean, renewable H-2 and O-2. However, improving the overall efficiency of water splitting is a challenging issue. Here, we designed Co-Fe nanoparticle coupled nitrogen-enriched porous carbon (CoyFe10-yOx/NPC) nanosheets as highly efficient non-precious-metal electrocatalysts for the oxygen evolution reaction (OER). Nitrogen-enriched porous carbon (NPC) nanosheets were prepared using a Schiff-base network (SNW) as the precursor and the SNW was based on commercially available and inexpensive monomers which were terephthalaldehyde and melamine. The resulting SNW possessed a high nitrogen content, a high surface area and a high density of metalcoordination sites. In addition, when used as the catalyst for the OER, the Co-Fe nanoparticle catalyst containing 30% Co (Co3Fe7Ox/NPC) showed the highest activity, requiring 328 mV over-potential to achieve a stable current density of 10 mA cm(-2) for at least 15 h and a small Tafel slope of 31.4 mV dec(-1) in 1.0 M KOH solution, which were comparable even superior to those of many other non-noble metal catalysts. Consequently, the high efficiency and durability make these supported amorphous Co-Fe nanoparticles potentially applicable for improving the performance for electrolysis of water and energy storage applications. More importantly, the support of electrode materials comes from the pyrolysis of porous polymers and this idea offers a new possibility for exploring overall water splitting non-precious-metal catalysts.
机译:水分解提供了生产清洁的,可再生的H-2和O-2的潜在途径。但是,提高水分解的整体效率是一个具有挑战性的问题。在这里,我们设计了Co-Fe纳米颗粒偶联的富氮多孔碳(CoyFe10-yOx / NPC)纳米片,作为用于氧气析出反应(OER)的高效非贵金属电催化剂。使用席夫碱网络(SNW)作为前体制备富氮多孔碳(NPC)纳米片,并且SNW基于对苯甲醛和三聚氰胺的市售廉价单体。所得的SNW具有高的氮含量,高的表面积和高的金属配位位点密度。此外,当用作OER的催化剂时,含30%Co(Co3Fe7Ox / NPC)的Co-Fe纳米颗粒催化剂表现出最高的活性,需要328 mV的超电势才能实现10 mA cm(- 2)在1.0 M KOH溶液中至少持续15 h和31.4 mV dec(-1)的小Tafel斜率,甚至可以媲美许多其他非贵金属催化剂。因此,高效率和耐久性使得这些负载的无定形Co-Fe纳米颗粒潜在地可用于改善水和能量存储应用的电解性能。更重要的是,电极材料的载体来自多孔聚合物的热解,这种想法为探索整体水分解非贵金属催化剂提供了新的可能性。

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