Fei Miao, Yantao Wang, Hongyu Zhou, Shuang Zhong, Jingkai Lin, Wen Xu, Xiting Yue, Wei Ren, Hui Zhang, Shaobin Wang, Jitraporn (Pimm) Vongsvivut, Xiaoguang Duan
Precise modulation of spin states of single-atom catalysts (SACs) offers a promising route to fine-tune peroxide activation behaviors and selectivity toward different oxidation pathways. Here, we report a spin-tunable Fe SAC composed of iron phthalocyanine (FePc) axially coordinated via oxygen bridges (-O-) onto annealed nanodiamond (AND), denoted as FePc-O-AND. The axial oxygen coordination induces a spin transition from high-spin (t2g5eg3) to an intermediate-spin (t2g4eg2) state. This transition generates an unoccupied Fe 3dz2 orbital that enables oriented electron transfer to peracetic acid (PAA) via hydroxyl oxygen coordination. In situ synchrotron-based Fourier-transform infrared spectroscopy (SR-FTIR) reveals a distinct PAA activation pathway involving inner-sphere complexation and a non-radical electron-transfer mechanism. As a result, the FePc-O-AND/PAA system drives a non-radical electron-transfer pathway with a high reaction rate (2.11 min−1), selectively converting phenolic pollutants into high-molecular-weight polyphenolic products (n ≥ 5). Density functional theory (DFT) calculations reveal that axial oxygen coordination in FePc-O-AND enhances PAA adsorption energy (−0.89 eV) and induces a favorable inner-sphere interaction with the hydroxyl oxygen, thereby facilitating effective PAA activation. The FePc-O-AND/PAA system exhibits strong resistance to water matrix interferences and maintains high performance over 130 h of continuous-flow operation. These findings establish axial coordination-mediated spin-state regulation as a powerful strategy for engineering SACs for sustainable water purification and recycling of micropollutants. By linking axial coordination chemistry to spin-state control and reactive oxygen species selectivity, this study delivers mechanistic insights and a versatile design principle for single-atom catalysts in environmental catalysis.