| Autor: |
Guangtai Han, Mengjiao Zhuansun, Tongbao Wang, Yuhang Wang |
| Jazyk: |
angličtina |
| Rok vydání: |
2024 |
| Předmět: |
|
| Zdroj: |
Advanced Materials Interfaces, Vol 11, Iss 3, Pp n/a-n/a (2024) |
| Druh dokumentu: |
article |
| ISSN: |
2196-7350 |
| DOI: |
10.1002/admi.202300760 |
| Popis: |
Abstract Effective electrocatalysts are crucial for facilitating the oxygen evolution reaction (OER), the anodic reaction of water electrolysis for renewable green hydrogen production. Perovskite oxides are a group of potential catalysts featuring the lattice oxygen mechanism (LOM) for OER, where O2 formation commences via a lattice oxygen redox process. The LOM pathway breaks the thermodynamic limitation of the adsorbate evolution mechanism (AEM) and achieves a high intrinsic activity. However, perovskite oxides often suffer high OER overpotentials due to the insufficient activation of the LOM pathway. Typically, the overpotential exceeds 300 mV at 10 mA cm−2. This greatly impedes the practical applications of perovskite oxide based OER catalysts. Here, it is demonstrated that the B‐site‐metal exsolution of a La0.6Sr0.4Fe0.8Ni0.2O3‐δ perovskite increases the activity of LOM by a factor of 3.8 at 400 mV overpotential. The activated LOM pathway leads to a 36‐mV reduction in the overpotential at 10 mA cm−2 (from 310 mV to 274 mV) and a 2× increase in the turnover frequency (TOF) at 450 mV overpotential. A membrane electrode assembly (MEA) water electrolyzer equipped with this LSFN‐based catalyst offers 1 A cm−2 current density at 2.46 V and 24‐h operation stability. |
| Databáze: |
Directory of Open Access Journals |
| Externí odkaz: |
|
Plný text