Bifunctional ligand Co metal-organic framework derived heterostructured Co-based nanocomposites as oxygen electrocatalysts toward rechargeable zinc-air batteries

• Published in: Journal of colloid and interface science 2024-06, Vol.664, p.319-328
• Main Authors: Xie, Xiaoying, Zhai, Zeyu, Cao, Weiwei, Dong, Jiamin, Li, Yushan, Hou, Qiusai, Du, Guixiang, Wang, Jiajun, Tian, Li, Zhang, Jingbo, Zhang, Tierui, Shang, Lu
• Format: Article
• Language: English
• Subjects: Cobalt oxide; Heterostructures; Metal-organic framework; Oxygen electrocatalysts; Zinc-air battery
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2024.03.040

A heterostructured Co-based electrocatalyst is successfully synthesized using bifunctional ligand Co metal–organic frameworks as precursors. The bifunctional ligands provide enough N and O atoms that can simultaneously convert Co ions into CoNx moieties, Co nanoparticles and Co oxides via one-step pyrolysis. The obtained electrocatalysts with heterostructured CoOx/Co nanoparticles encapsulated by porous conductive carbon rich in CoNx active sites deliver remarkable oxygen reduction reaction and oxygen evolution reaction activities. With the synergistic effects among these multifunctional components, a rechargeable zinc–air battery built with this electrocatalyst exhibits a high-power density and long-lasting rechargeability. [Display omitted] Rational construction of efficient and robust bifunctional oxygen electrocatalysts is key but challenging for the widespread application of rechargeable zinc-air batteries (ZABs). Herein, bifunctional ligand Co metal–organic frameworks were first explored to fabricate a hybrid of heterostructured CoOx/Co nanoparticles anchored on a carbon substrate rich in CoNx sites (CoOx/Co@CoNC) via a one-step pyrolysis method. Such a unique heterostructure provides abundant CoNx and CoOx/Co active sites to drive oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), respectively. Besides, their positive synergies facilitate electron transfer and optimize charge/mass transportation. Consequently, the obtained CoOx/Co@CoNC exhibits a superior ORR activity with a higher half-wave potential of 0.88 V than Pt/C (0.83 V vs. RHE), and a comparable OER performance with an overpotential of 346 mV at 10 mA cm−2 to the commercial RuO2. The assembled ZAB using CoOx/Co@CoNC as a cathode catalyst displays a maximum power density of 168.4 mW cm−2, and excellent charge–discharge cyclability over 250 h at 5 mA cm−2. This work highlights the great potential of heterostructures in oxygen electrocatalysis and provides a new pathway for designing efficient bifunctional oxygen catalysts toward rechargeable ZABs.