4.7 Article

Robust bifunctional phosphorus-doped perovskite oxygen electrode for reversible proton ceramic electrochemical cells

期刊

CHEMICAL ENGINEERING JOURNAL
卷 450, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.137787

关键词

Oxygen electrode; Phosphorus doping; Protonic ceramic electrochemical cells; Oxygen reduction reaction; Water oxidation reaction

资金

  1. National Natural Science Foundation of China [21878158, 21706129]

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Driven by the demand for sustainable energy, reversible proton ceramic electrochemical cells (R-PCECs) have attracted attention. However, the low activity and poor durability of the oxygen electrode limit their large-scale application. In this study, a novel oxygen electrode material with high activity and stability is developed through partial doping of non-metallic phosphorus. The results show promising potential for non-metal-doped oxygen electrode materials in practical R-PCECs.
Driven by the demand for the sustainable regeneration of clean energy and high-efficiency low-cost energy conversion equipment, reversible proton ceramic electrochemical cells (R-PCECs), which are promising for realizing the mutual conversion between large-scale renewable electric energy and chemical energy, are receiving constant attention. Unfortunately, the sluggish activity of oxygen reduction reaction (ORR) and water oxidation reaction (WOR) for the oxygen electrode in the low and medium temperature ranges and the poor durability of reversible operation block the large-scale application of R-PCECs. Here, a novel oxygen electrode Ba0.5Sr0.5(Co0.8Fe0.2)0.95P0.05O3-delta (BSCFP0.05) with high electrochemical activity and stability is developed. By partially doping non-metallic phosphorus (P) element into the B-site transition metal of the classic oxygen electrode Ba0.5Sr0.5Co0.8Fe0.2O3-delta (BSCF), the electronic conductivity, ions (O2-/H+) transport capacity, and hydration ability are all significantly boosted. Especially, a single cell with the BSCFP0.05 electrode achieves an excellent peak power density of 842 mW cm-2 and an electrolysis current of -1000 mA cm-2 at 1.3 V at 600 degrees C. No significant attenuation appears during continuous conversion operation between the fuel cell model and the electrolysis cell model for up to 240 h with the BSCFP0.05 oxygen electrode. These results highly promise nonmetal-doped oxygen electrode materials in practical R-PCECs.

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