Designing High-Quality Electrocatalysts Based on CoO:MnO2@C Supported on Carbon Cloth Fibers as Bifunctional Air Cathodes for Application in Rechargeable Zn–Air Battery

双功能 材料科学 电化学 电催化剂 电池(电) 阴极 析氧 碳纤维 化学工程 纳米技术 电极 催化作用 复合材料 化学 物理化学 有机化学 复合数 功率(物理) 工程类 物理 量子力学
作者
Mohammad‐Reza Zamani‐Meymian,Karim Khanmohammadi Chenab,Hamed Pourzolfaghar
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (50): 55594-55607 被引量:10
标识
DOI:10.1021/acsami.2c16826
摘要

To achieve the requirements of rechargeable Zn-air batteries (ZABs), designing efficient, bifunctional, stable, and cost-effective electrocatalysts is vital for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), which still are struggling with unsolved challenges. The present research provides a concept based on the nanoscale composites which were engineered by using MnO2@C, CoO@C, and CoO:MnO2@C bifunctional electrocatalysts for fabrication of uniform carbon cloth (CC)-based electrodes. The CoO:MnO2@C electrocatalyst represented more efficient electrochemical properties through ORR and OER processes with superior positive half-wave potential (E1/2 = 0.78 V) and better limiting current density (i = 1.10 mA cm-2) in comparison with MnO2@C (E1/2 = 0.71 V, i = 0.92 mA cm-2) and CoO@C (E1/2 = 0.69 V, i = 0.86 mA cm-2) electrocatalysts. For the rechargeable ZABs fabricated by using CoO:MnO2@C-CC as an O2-breathing cathode, the specific capacity (SC), peak power density (P), open-circuit voltage (EOCV), and gap of charge/discharge voltage resulted in values of 520 mAh gZn-1, 210.0 mW cm-2, and 1.45 and 0.45 V, respectively, that afforded greater electrochemical characters than what was obtained for ZABs based on MnO2@C-CC (410 mAh gZn-1, 195.0 mW cm-2, 1.38 and 0.44 V) and CoO@C-CC (440 mAh gZn-1, 165.0 mW cm-2, 1.15 and 0.54 V). At the same time, lower Ei=10 (= 1.45 V) implied a more efficient OER in alkaline electrolyte solution for CoO:MnO2@C than MnO2@C (Ei=10 = 1.50 V) and CoO@C (Ei=10 = 1.39 V). Based on cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and X-ray photoelectron spectroscopy (XPS) results, it could be stated that the CoO:MnO2@C catalytic surface could experience 30 and 32% lower charge transfer resistance (Rct = 13.9 Ω) than MnO2@C (Rct = 20.1 Ω) and CoO@C (Rct = 29.7 Ω), respectively, which empowers an enhancement in ORR/OER performance. Prominently, the design concept of proposed electrocatalysts could suggest clear horizon for the synthesis and development paradigms of bifunctional catalysts for energy storage materials and devices.
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