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源自双核壳结构CNH@PDA@NiMOFs的镍基纳米颗粒嵌入氮掺杂碳纳米角用于氧电催化

Ni-Based Nanoparticle-Embedded N-Doped Carbon Nanohorns Derived from Double Core-Shell CNH@PDA@NiMOFs for Oxygen Electrocatalysis.

作者信息

Guo Yanli, Zhou Yun, Nan Yanli, Li Bo, Song Xiaolong

机构信息

State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an 710049, China.

School of Medical Information and Engineering, Southwest Medical University, Luzhou 646000, China.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 18;12(11):12743-12754. doi: 10.1021/acsami.9b20532. Epub 2020 Mar 5.

Abstract

The development of highly efficient electrocatalysts for the oxygen evolution reaction (OER) plays a crucial role in many regenerative electrochemical energy-conversion systems. Herein, we report a novel double core-shell-structured CNH@PDA@NiMOF (CNH-D-NiMOF) composite based on the support of carbon nanohorns (CNHs) and the direction of polydopamine (PDA) on the synthesis of metal-organic frameworks (MOFs). It is found that this unique structure improves the electrocatalytic performance and stability of the composites. Furthermore, a controlled partial pyrolysis strategy was proposed to construct the Ni-based nanoparticle-embedded N-doped CNHs. The partial pyrolysis method preserves the framework structure of MOFs for effective substrate diffusion while producing highly active nanoparticles. This leads to the result that the Ni-based nanoparticle-embedded N-doped CNHs possess higher stability and significantly improved electrocatalytic properties. Among these derivatives, the sample prepared at a pyrolysis temperature of 400 °C (named as CNH-D-NiMOF-400) outperforms most of the reported unprecious-metal catalysts. At current densities of 20 and 100 mA·cm, the overpotentials of CNH-D-NiMOF-400 are 270 and 340 mV for the OER on a carbon fiber paper (CFP), respectively. The outstanding electrocatalytic properties above suggest that this composite is an excellent candidate for the substitution of noble metal-based catalysts for OER.

摘要

开发用于析氧反应(OER)的高效电催化剂在许多可再生电化学能量转换系统中起着至关重要的作用。在此,我们报告了一种基于碳纳米角(CNHs)支撑和聚多巴胺(PDA)导向合成金属有机框架(MOFs)的新型双核壳结构CNH@PDA@NiMOF(CNH-D-NiMOF)复合材料。发现这种独特结构提高了复合材料的电催化性能和稳定性。此外,提出了一种可控的部分热解策略来构建嵌入镍基纳米颗粒的氮掺杂CNHs。部分热解方法保留了MOFs的框架结构以实现有效的底物扩散,同时产生高活性的纳米颗粒。这导致嵌入镍基纳米颗粒的氮掺杂CNHs具有更高的稳定性和显著改善的电催化性能。在这些衍生物中,在400℃热解温度下制备的样品(命名为CNH-D-NiMOF-400)优于大多数已报道的非贵金属催化剂。在碳纤维纸(CFP)上进行OER时,在20和100 mA·cm的电流密度下CNH-D-NiMOF-400的过电位分别为270和340 mV。上述出色的电催化性能表明这种复合材料是替代用于OER的贵金属基催化剂的极佳候选材料。

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