Yuan Geng, Ruiz Pestana Luis
Department of Chemical, Environmental and Materials Engineering, University of Miami, Coral Gables, FL 33146, USA.
Department of Civil and Architectural Engineering, University of Miami, Coral Gables, FL 33146, USA.
Nanomaterials (Basel). 2024 Jun 19;14(12):1058. doi: 10.3390/nano14121058.
Developing cost-effective and highly active electrocatalysts for the oxygen evolution reaction (OER) is crucial for advancing sustainable energy applications. High-entropy alloys (HEAs) made from earth-abundant transition metals, thanks to their remarkable stability and electrocatalytic performance, provide a promising alternative to expensive electrocatalysts typically derived from noble metals. While pristine HEA surfaces have been theoretically investigated, and the effect of oxygen coverage on conventional metal electrocatalysts has been examined, the impact of surface oxygen coverage on the electrocatalytic performance of HEAs remains poorly understood. To bridge this gap, we employ density functional theory (DFT) calculations to reconstruct the free energy diagram of OER intermediates on CoFeNiCr HEA surfaces with varying oxygen coverages, evaluating their impact on the rate-limiting step and theoretical overpotential. Our findings reveal that increased oxygen coverage weakens the adsorption of HO* and O*, but not HOO*. As a result, the theoretical overpotential for the OER decreases with higher oxygen coverage, and the rate-limiting step shifts from the third oxidation step (HOO* formation) at low coverage to the first oxidation step (HO* formation) at higher coverage.
开发用于析氧反应(OER)的具有成本效益且高活性的电催化剂对于推进可持续能源应用至关重要。由储量丰富的过渡金属制成的高熵合金(HEA),由于其卓越的稳定性和电催化性能,为通常由贵金属衍生的昂贵电催化剂提供了一种有前景的替代方案。虽然已从理论上研究了原始HEA表面,并且研究了氧覆盖对传统金属电催化剂的影响,但表面氧覆盖对HEA电催化性能的影响仍知之甚少。为了弥补这一差距,我们采用密度泛函理论(DFT)计算来重建具有不同氧覆盖度的CoFeNiCr HEA表面上OER中间体的自由能图,评估它们对速率限制步骤和理论过电位的影响。我们的研究结果表明,增加的氧覆盖会削弱HO和O的吸附,但不会削弱HOO的吸附。因此,OER的理论过电位随着氧覆盖度的增加而降低,并且速率限制步骤从低覆盖度下的第三步氧化(HOO形成)转变为高覆盖度下的第一步氧化(HO*形成)。