Liu Christopher Pantayatiwong, Vang Ethan Hwjchim, Priamushko Tatiana, Roiron Camille, Cherevko Serhiy, Atanassov Plamen
Department of Chemical and Biomolecular Engineering, University of California, Irvine, California 92697, United States.
Helmholtz-Institute Erlangen-Nürnberg for Renewable Energy (IET-2), Forschungszentrum Jülich, Erlangen 52428, Germany.
ACS Catal. 2025 Apr 29;15(10):7956-7965. doi: 10.1021/acscatal.5c00523. eCollection 2025 May 16.
Cu and Mn was incorporated into Co spinels and the structural and electrochemical properties of the resulting materials were investigated. Cu and Mn were found to reside exclusively in the octahedral sites in the spinel lattice. The incorporation of Mn and especially Cu improved initial activity for the oxygen evolution reaction in an acidic environment. The Mn-containing catalysts demonstrated substantially improved potential cycling durability. This was explained through cyclic voltammetry and online inductively coupled plasma mass spectrometry (ICP-MS) by the role of Mn on limiting the oxidation of tetrahedrally coordinated Co. In potentiostatic conditions, however, pure Co spinel outperformed the multimetal oxides over time. In total, these findings stress the importance of stabilizing the tetrahedral Co site through incorporation of other elements, and the improvements in electrochemical activity and stability that can thereby be realized.
将铜和锰掺入钴尖晶石中,并对所得材料的结构和电化学性能进行了研究。发现铜和锰仅存在于尖晶石晶格的八面体位置。锰尤其是铜的掺入提高了在酸性环境中析氧反应的初始活性。含锰催化剂的电位循环耐久性有了显著提高。通过循环伏安法和在线电感耦合等离子体质谱(ICP-MS)解释了锰在限制四面体配位钴氧化方面的作用。然而,在恒电位条件下,随着时间的推移,纯钴尖晶石的性能优于多金属氧化物。总的来说,这些发现强调了通过掺入其他元素来稳定四面体钴位点的重要性,以及由此可以实现的电化学活性和稳定性的提高。