Formation of Hierarchical Zn/N‐doped Carbon Hollow Nanofibers towards Dendrite‐Free Zn Metal Anodes

Author:

Yu Huan1,Yao Haixin1,Zheng Yaqi1,Liu Dan2,Chen Jun Song3ORCID,Guo Yan2ORCID,Li Nian Wu1ORCID,Yu Le1ORCID

Affiliation:

1. State Key Lab of Organic‐Inorganic Composites Beijing University of Chemical Technology Beijing 100029 P. R. China

2. School of Chemistry and Chemical Engineering Inner Mongolia University Hohhot 010021 P. R. China

3. School of Materials and Energy University of Electronic Science and Technology of China Chengdu 611731 P. R. China

Abstract

AbstractRechargeable aqueous Zn metal batteries are considered as promising next‐generation energy storage device because of their intrinsic safety and low cost. Nonetheless, the poor lifespan stemming from uncontrollable dendrite growth and inevitable parasitic reactions of metallic Zn impede their large‐scale application. Herein, the formation of the hierarchical lotus root‐like Zn/N‐doped carbon hollow nanofibers‐based paper is reported decorated with interconnected Zn/N‐doped carbon nanocages (denoted as LRZCF@ZCC) as a freestanding host with multifunctionality for Zn metal anode. Of note, the interconnected porous structure mitigates the internal stress to ensure robust structure. Besides, the concave surface of inner LRZCF@ZCC channel facilitates the nucleation of Zn2+ to geometrically guide the Zn deposition. Meanwhile, the well‐distributed metallic Zn and N‐doped carbon species can serve as the zincophilic sites to reduce the nucleation overpotential and avoid the evolution of hydrogen bubbles. As expected, the LRZCF@ZCC exhibits low polarization for the controllable Zn deposition with small voltage hysteresis. Both the symmetric cell and the full cell using this unique host demonstrate long‐term cycling duration and enhanced rate capability.

Funder

National Natural Science Foundation of China-Shandong Joint Fund

Publisher

Wiley

Subject

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

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