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Highly stable nitrogen-doped carbon nanotubes derived from carbon dots and metal-organic frameworks toward excellent efficient electrocatalyst for oxygen reduction reaction

机译:高稳定的氮掺杂碳纳米管衍生自碳点和金属有机框架,朝向优异的有效电催化剂进行氧还原反应

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摘要

A highly efficient nitrogen-doped carbon nanotubes (N-CNTs) electrocatalyst derived from nitrogen-doped carbon dots (N-Cdots) and metal-organic frameworks (MOFs) for oxygen reduction reaction (ORR) was demonstrated successfully for the first time. The N-Cdots with plenty of hydroxyl and amine groups can favor the formation of N-CNTs through the catalytic decomposition of MOFs in a lower temperature. On the other hand, the N-Cdots serve as inducers of the graphitic structure and supply extra nitrogen, extending a potential electrocatalytic activity of N-CNTs. Results show that the N-CNTs provided an excellent ORR electrocatalytic performance, yielding a positive onset potential of 0.88 V vs. RHE and a high kinetic current density of up to 5.58 mA cm(-2) at 0.2 V. In addition, the slope of N-CNTs being similar to 81 mV/dec can be found to be much lower than that of the Pt/C catalyst (similar to 132 mV/dec). These superior performances are attributed to defects in the graphitic crystal structure and the synergistic coupling effects of N-Cdots and N-CNTs. In addition, a slight loss in activity for the N-CNTs catalyst can be found whereas the Pt/C catalyst decreases nearly 45% of its initial activity, which exhibit highly catalytic durability and tolerance to methanol in an alkaline media.
机译:首次证明了衍生自氮掺杂碳点(N-Cdots)的高效氮掺杂碳纳米管(N-CNT)电催化剂和用于氧还原反应(ORR)的金属 - 有机框架(MOF)。具有大量羟基和胺基团的N- Cdots可以通过在较低温度下通过MOF的催化分解形成N-CNT。另一方面,N-CADOTS用作石墨结构的诱导剂和供应额外的氮气,延伸了N-CNT的潜在电催化活性。结果表明,N-CNT提供了优异的ORR电催化性能,产生0.88V与RHE的正发作电位和高达5.58 mA cm(-2)的高动力电流密度为0.2V。另外,斜坡可以发现类似于81 MV / DEC的N-CNT,远低于PT / C催化剂(类似于132mV / DEC)。这些优异的性能归因于石墨晶体结构的缺陷和N-CDOTS和N-CNT的协同偶联效果。此外,可以发现N-CNT催化剂的活性的轻微损失,而Pt / C催化剂降低其初始活性的近45%,其表现出高度催化的耐久性和对碱性介质中甲醇的耐受性。

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