Self‐Assembled 3D N/P/S‐Tridoped Carbon Nanoflower with Highly Branched Carbon Nanotubes as Efficient Bifunctional Oxygen Electrocatalyst Toward High‐Performance Rechargeable Zn‐Air Batteries

Author:

Chang Hui12,Liu Xinyu1,Zhao Shan1,Liu Zonglin1,Lv Ruitao3,Zhang Qianyu234ORCID,Yi Ting‐Feng15

Affiliation:

1. School of Materials Science and Engineering Northeastern University Shenyang 110819 China

2. Engineering Research Center of Alternative Energy Materials and Devices Ministry of Education College of Materials Science and Engineering Sichuan University Chengdu 610064 China

3. Key Laboratory of Advanced Materials of Ministry of Education Tsinghua University Beijing 100084 China

4. 21C Innovation Laboratory Contemporary Amperex Technology Ltd. (21C LAB) Ningde 352100 China

5. Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province School of Resources and Materials Northeastern University at Qinhuangdao Qinhuangdao 066004 China

Abstract

AbstractHeteroatom doping and 3D nanostructures with large specific surface area and hierarchical porous structure can synergically improve oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). In this study, the 3D N/P/S‐tridoped nanoflower with highly branched carbon nanotubes bifunctional catalyst (Co/SP‐NC) is prepared by a simple self‐assembly pyrolysis method. The powerful driving force of coordination interaction of ammonium ion can promote the self‐assembly of 2D ZnCo‐ZIF nanosheets into 3D ZnCo/S‐ZIF nanoflowers at room temperature stirring. The 3D ZnCo/S‐ZIF nanoflower surface is driven by sodium hypophosphite to form highly branched carbon nanotubes during the pyrolysis process. Moreover, Density functional theory (DFT) calculations also confirm that the simultaneous introduction of N/P/S can promote the redistribution of electron density at the catalyst interface. The proper P‐doping not only enhances the electronic conductivity of the substrate, but also facilitates the charge transfer in the OER/ORR process. Therefore, Co/SP‐NC cathode assembled zinc‐air batteries (ZABs) have a higher power density (187 mW cm−2), a larger specific capacity (801 mAh gZn−1) and excellent cycle stability compared to Pt/C‐RuO2 assembled ZABs. This work will pave the way to regulate the components interactions by designing 3D hierarchical porous structures.

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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