Optimizing the Ru Catalyst–Support Interaction via Tunnel Size of MnO<sub>2</sub> Support for Enhanced Acidic Water Oxidation
Sixuan She, Changsheng Chen, Ke Fan, Gao Chen, Yanping Zhu, Daqin Guan, Yucheng Huang, Hsiao‐Chien Chen, Zezhou Lin, Hon Fai Wong, Liuqing Li, Ye Zhu, Chi Wah Leung, Yuen Hong Tsang, Haitao Huang
Abstract
Metal–support interaction (MSI) has profound impacts on the catalytic performance of heterogeneous catalysts. Rational modulation of MSI will give rise to unusually high activity and stability. Here, we demonstrate that the MSI strength can be effectively tuned by the tunnel size of MnO 2 supports to help address the two fundamental challenges in Ru-based acidic oxygen evolution reaction (OER): the sluggish kinetics and the instability of Ru sites. Through crystallographic engineering from α-MnO 2 to β-MnO 2 polymorphs, we found that the reduced tunnel size of MnO 2 increases planar oxygen (O pla ) concentration and promotes the formation of strong Ru–O pla –Mn bonds, thereby enhancing the Ru/MnO 2 interactions. However, an excessively small tunnel size in β-MnO 2 leads to surface amorphization and elongated Ru–O pla –Mn bonds after Ru incorporation, thus reversely weakening the Ru/MnO 2 interactions. Our work manifests distinct volcano-shaped dependencies for both MSI strength and OER activity as a function of the tunnel size of MnO 2 supports. The optimized Ru-γ-MnO 2 catalyst, featuring an intermediate tunnel size and the strongest MSI, achieves an exceptional mass activity (1743 A g –1 at 1.5 V) while maintaining a high stability. Our results suggest that strong Ru–O pla –Mn interactions promote the formation of the OOH* intermediate through high Ru–O covalency and stabilize reactive Ru species against dissolution through double-exchange charge transfer from low-valence Mn sites. These findings offer valuable insights into the modulation of MSI via structural design of support for the optimization of other supported catalysts.