Dynamic Co(II)/Co(III) Cycle Driven by Outer- and Inner-Sphere Electron Transfer for Sustained Peroxymonosulfate Activation
Ning An, Nan Chen, Chuanping Feng, S. F. Zhang, Zhe Li, Tong Liu, Yang Liu, Wang Lu, Zhengyuan Feng, Hang Gao, Hui-Jun Mu, Miao Li
Abstract
In the realm of transition metal (M n + ) activated peroxymonosulfate (PMS), sluggish reduction kinetics of M ( n +1)+ often lead to the rapid deactivation of catalytic centers, posing a significant challenge for commercialization of homogeneous advanced oxidation processes (AOPs). We report a pioneering elucidation of a distinct Co(II)/Co(III) cycling mechanism within electrochemically enhanced PMS-AOPs, utilizing Co(II) as a model catalyst. Remarkably, this cycling process predominantly unfolds in the anodic region, rather than the cathodic, revealing a novel aspect of electrochemical modulation. Co(III), generated by anodic oxidation, emerges as a pivotal species that disrupts the dimerized hydrolysis product ([Co(III)OH] 2 4+ ). Electron transfer from the hydroxyl oxygen in [Co(III)OH] 2 4+ to Co(III) induces electron redistribution, ultimately facilitating Co(III) reduction and release via both outer- and inner-sphere electron transfer pathways. Gibbs free energy calculations unequivocally confirm the spontaneity of the cyclic process. Our system exhibits superior performance metrics, achieving Co(IV)═O (5.57 × 10 –2 mM/M Co) and SO 4 •– (2.51 × 10 –6 mM/M OSO 3 ) yields that surpass most reported catalytic systems, along with an exceptional mass activity of Co(II) (368.87 L/g). This study offers a fresh perspective on M n + regeneration for sustained PMS activation in homogeneous transition metal catalysis, with potential implications for advancing the field of environmental remediation.