Han Jingrui, Wang Haibin, Wang Yuting, Zhang Hao, Li Jun, Xia Yujian, Zhou Jieshu, Wang Ziyun, Luo Mingchuan, Wang Yuhang, Wang Ning, Cortés Emiliano, Wang Zumin, Vomiero Alberto, Huang Zhen-Feng, Ren Hangxing, Yuan Xianming, Chen Songhua, Feng Donghui, Sun Xuhui, Liu Yongchang, Liang Hongyan
School of Materials Science and Engineering, Tianjin University, Tianjin, 300350, P.R. China.
School of Science, Tianjin University, Tianjin, 300350, P.R. China.
Angew Chem Int Ed Engl. 2024 Aug 12;63(33):e202405839. doi: 10.1002/anie.202405839. Epub 2024 Jul 4.
Triggering the lattice oxygen oxidation mechanism is crucial for improving oxygen evolution reaction (OER) performance, because it could bypass the scaling relation limitation associated with the conventional adsorbate evolution mechanism through the direct formation of oxygen-oxygen bond. High-valence transition metal sites are favorable for activating the lattice oxygen, but the deep oxidation of pre-catalysts suffers from a high thermodynamic barrier. Here, taking advantage of the Jahn-Teller (J-T) distortion induced structural instability, we incorporate high-spin Mn ( ) dopant into CoN. Mn dopants enable a surface structural transformation from CoN to CoOOH, and finally to CoO, as observed by various in situ spectroscopic investigations. Furthermore, the reconstructed surface on Mn-doped CoN triggers the lattice oxygen activation, as evidenced experimentally by pH-dependent OER, tetramethylammonium cation adsorption and online electrochemical mass spectrometry measurements of O-labelled catalysts. In general, this work not only offers the introducing J-T effect approach to regulate the structural transition, but also provides an understanding about the influence of the catalyst's electronic configuration on determining the reaction route, which may inspire the design of more efficient catalysts with activated lattice oxygen.
触发晶格氧氧化机制对于提高析氧反应(OER)性能至关重要,因为它可以通过直接形成氧-氧键绕过与传统吸附质演化机制相关的比例关系限制。高价过渡金属位点有利于激活晶格氧,但预催化剂的深度氧化存在较高的热力学势垒。在此,利用 Jahn-Teller(J-T)畸变引起的结构不稳定性,我们将高自旋 Mn( )掺杂剂引入 CoN 中。各种原位光谱研究观察到,Mn 掺杂剂使表面结构从 CoN 转变为 CoOOH,最终转变为 CoO。此外,Mn 掺杂 CoN 上重构的表面触发了晶格氧的活化,pH 依赖的 OER、四甲基铵阳离子吸附以及 O 标记催化剂的在线电化学质谱测量实验证明了这一点。总的来说,这项工作不仅提供了引入 J-T 效应来调节结构转变的方法,还提供了对催化剂电子构型对确定反应路线影响的理解,这可能会激发设计具有活化晶格氧的更高效催化剂。