Ruan Qingqing, Lu Shanshan, Wu Jiaqi, Shi Yanmei, Zhang Bin
Institute of Molecular Plus, Department of Chemistry, School of Science, Tianjin University, Tianjin, 300072, China.
Angew Chem Int Ed Engl. 2024 Aug 26;63(35):e202409000. doi: 10.1002/anie.202409000. Epub 2024 Jul 24.
M-N-C single-atom catalysts (SACs) are promising electrode materials for many electro-reduction reactions. However, their stability is far from practical applications, and their deactivation mechanism has been rarely investigated. Herein, we demonstrate the structural degradation of M-N-C (M=Co, Ni, and Fe) at industrial-grade current density for long-term electro-reduction. Both M-N and N-C bonds are broken, resulting in the gradual hydrogenation and dissolution of N in the form of ammonia. The residual M is finally converted to M-containing core-shell nanoparticles after sequential dissolution, redeposition, and electro-reduction. The destruction of the M-N-C structure and the formation of nanoparticles greatly affect the electrocatalytic performance. Our work highlights the structural degradation and deactivation mechanism of M-N-C-type SACs under strong reductive conditions and provides useful information for inspiring researchers to develop new strategies to improve the electrocatalytic stability of similar types of materials.
M-N-C单原子催化剂(SACs)是许多电还原反应中很有前景的电极材料。然而,它们的稳定性远未达到实际应用水平,其失活机制也鲜有研究。在此,我们展示了M-N-C(M = 钴、镍和铁)在工业级电流密度下长期电还原时的结构降解。M-N键和N-C键均断裂,导致氮以氨的形式逐渐氢化和溶解。残余的M最终在经历连续溶解、再沉积和电还原后转化为含M的核壳纳米颗粒。M-N-C结构的破坏和纳米颗粒的形成极大地影响了电催化性能。我们的工作突出了M-N-C型SACs在强还原条件下的结构降解和失活机制,并为激励研究人员开发新策略以提高类似材料的电催化稳定性提供了有用信息。