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负载于纳米多孔金属有机骨架纳米片上的氮、磷共掺杂碳纳米管包覆的钴/钴磷纳米颗粒用于氧还原和析氧反应

Co/CoP Nanoparticles Encapsulated Within N, P-Doped Carbon Nanotubes on Nanoporous Metal-Organic Framework Nanosheets for Oxygen Reduction and Oxygen Evolution Reactions.

作者信息

Yang Xinxin, Mi Hongwei, Ren Xiangzhong, Zhang Peixin, Li Yongliang

机构信息

College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518060, Guangdong, People's Republic of China.

Guangdong Flexible Wearable Energy Tools Engineering Technology Research Centre, Shenzhen University, Shenzhen, 518060, Guangdong, People's Republic of China.

出版信息

Nanoscale Res Lett. 2020 Apr 15;15(1):82. doi: 10.1186/s11671-020-03316-x.

Abstract

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 and the Tafel slope of 74 mV dec 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. After 9 h, the current density is only decreased by 10%, which is far less than the loss of RuO. 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.

摘要

在此,通过煅烧以及随后的磷化处理,获得了由原子层沉积的六方金属有机框架(MOF)衍生的N、P掺杂碳纳米管包裹的Co/CoP纳米颗粒,并将其用作电催化剂。电催化性能评估表明,所制备的电催化剂在10 mA cm的电流密度下,析氧反应(OER)的过电位为342 mV,塔菲尔斜率为74 mV dec,优于最先进的氧化钌电催化剂。该电催化剂还表现出比基准RuO更好的稳定性。9小时后,电流密度仅降低了10%,远低于RuO的损失。此外,其氧还原反应(ORR)的起始电位为0.93 V,并遵循理想的4电子途径。稳定性测试后,电催化剂的电流密度保留了初始值的94%,优于Pt/C。上述结果表明,该电催化剂对OER和ORR均具有双功能活性和优异的稳定性。相信该策略为磷化钴/碳基电催化剂的合成提供了指导。

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