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首页> 外文期刊>Nanoscale Research Letters >Co/CoP Nanoparticles Encapsulated Within N, P-Doped Carbon Nanotubes on Nanoporous Metal-Organic Framework Nanosheets for Oxygen Reduction and Oxygen Evolution Reactions
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Co/CoP Nanoparticles Encapsulated Within N, P-Doped Carbon Nanotubes on Nanoporous Metal-Organic Framework Nanosheets for Oxygen Reduction and Oxygen Evolution Reactions

机译:CO / COP纳米颗粒包封在n,p掺杂的碳纳米管内,纳米多孔金属 - 有机框架纳米片内纳米液进行氧还原和氧气进化反应

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Herein, Co/CoP nanoparticles encapsulated with N, P-doped carbon nanotubes derived from the atomic layer deposited hexagonal metal-organic frameworks (MOFs) are obtained by calcinations and subsequent phosphating and are employed as electrocatalyst. The electrocatalytic performance evaluations show that the as-prepared electrocatalyst exhibits an overpotential of 342?mV at current density of 10?mA?cm~(?2)and the Tafel slope of 74?mV dec~(?1)for oxygen evolution reaction (OER), which is superior to the most advanced ruthenium oxide electrocatalyst. The electrocatalyst also shows better stability than the benchmark RuO_(2). After 9?h, the current density is?only decreased by 10%, which is far less than the loss of RuO_(2). Moreover, its onset potential for oxygen reduction reaction (ORR) is 0.93?V and follows the ideal 4-electron approach. After the stability test, the current density of the electrocatalyst retains 94% of the initial value, which is better than Pt/C. The above results indicate that the electrocatalyst has bifunctional activity and excellent stability both?for OER and ORR. It is believed that this strategy provides guidance for the synthesis of cobalt phosphide/carbon-based electrocatalysts.
机译:这里,通过煅烧和随后的磷化获得与原子层沉积的六边形金属 - 有机骨架(MOF)衍生的N,P掺杂碳纳米管包封的CO / COP纳米颗粒是通过煅烧和随后的磷化获得的,并且用作电催化剂。电催化性能评价表明,当氧化反应的氧化反应的电流密度为342Ω·mV的过电容器,其具有342Ω·mV的过电容器,为74μm〜(α1)的氧化反应(oer),优于最先进的氧化钌电催化剂。电催化剂还显示比基准Ru_(2)更好的稳定性。在9℃之后,电流密度是α仅减少10%,远低于Ru_(2)的损失。此外,其发病氧还原反应(ORR)的潜力为0.93Ωv并遵循理想的4-电子方法。在稳定性测试之后,电催化剂的电流密度保留了初始值的94%,其优于Pt / c。上述结果表明,电催化剂具有双功能活性和优异的稳定性?对于oer和Orr。据信,该策略为合成磷化钴/碳基电催化剂提供了指导。

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