Engineering efficient bifunctional electrocatalysts for rechargeable zinc-air batteries by confining Fe-Co-Ni nanoalloys in nitrogen-doped carbon nanotube@nanosheet frameworks

被引:70
|
作者
Tang, Xiannong [1 ]
Cao, Rui [2 ]
Li, Longbin [1 ]
Huang, Bingyu [1 ]
Zhai, Weijuan [1 ]
Yuan, Kai [1 ]
Chen, Yiwang [1 ,3 ]
机构
[1] Nanchang Univ, Coll Chem, Inst Polymers & Energy Chem IPEC, Nanchang 330031, Jiangxi, Peoples R China
[2] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource SSRL, Menlo Pk, CA 94025 USA
[3] Jiangxi Normal Univ, Inst Adv Sci Res iASR, Nanchang 330022, Jiangxi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
OXYGEN REDUCTION; POROUS CARBONS; EVOLUTION; CATALYSTS; ALLOY; IDENTIFICATION;
D O I
10.1039/d0ta09580j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing precious-metal-free bifunctional oxygen reduction and evolution reaction (ORR/OER) electrocatalysts is of great significance for several key energy conversion and storage systems, yet remains a formidable challenge. Herein, we systematically designed Fe-Co-Ni trimetallic nanoalloys encapsulated in nitrogen-doped carbon nanotube@nanosheet frameworks (FeCoNi-NC) for application as effective bifunctional ORR/OER electrocatalysts. The rational structural design of FeCoNi-NC provides hierarchical porosity coupled with greatly increased effective electrochemical specific area for exposing abundant active sites and enhanced mass-transfer capability toward the ORR/OER. Experimental observations and theoretical calculations confirmed that Fe-Co-Ni nanoalloys interacting with pyridinic nitrogen-rich carbon synergistically optimized the adsorption/desorption free energies of oxygen intermediates, thus significantly enhancing the intrinsic ORR/OER activity. Consequently, FeCoNi-NC exhibits remarkable bifunctionality for the ORR (half-wave potential of 0.89 V) and OER (1.54 V at 10 mA cm(-2)) with Delta E = 0.65 V, and even outperforms Pt/C-RuO2 benchmarks. Moreover, the corresponding zinc-air battery shows large power density (315.2 mW cm(-2)), high capacity (803.78 mA h g(-1) at 100 mA cm(-2)) and excellent cycling durability (over 100 hours at 50 mA cm(-2)), further testifying its practical applications. This work demonstrates an effective pathway to highly active non-precious-metal bifunctional catalysts toward sustainable energy technologies.
引用
收藏
页码:25919 / 25930
页数:12
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