摘要： The exploration of nonprecious metal-based electrocatalysts with high efficiency for the triiodide reduction is critical for the practical applications of the dye-sensitized solar cells. Herein, we develop a facile one-step hydrothermal method to synthesize hollow hierarchical structure Co0.85Se. Under the methanol-water reaction system, the product named as hollow hierarchical structure Co0.85Se-M has the largest specific surface area (215.36 m2 g?1) and the best crystallinity than other products obtained from other alcohol-water reaction systems. When this electrocatalyst is applied as a counter electrode for the dye-sensitized solar cells, it exhibits a small peak-to-peak separation (Epp, 97 mV) for the reduction of I3?/I? redox couple. It is found that the catalytic activity of Co0.85Se is closely dependent on the crystallinity. Moreover, the reactivity pathway is identified by density functional theory, which confirms that triiodide is reduced to iodide ion on Co0.85Se with a smaller energy barrier (～0.65 eV) than on Pt (～1.18 eV). Both experimental and theoretical results demonstrate Co0.85Se-M as an ideal counter electrode material for the dye-sensitized solar cells with a higher power conversion efficiency (8.76%) than Pt counter electrode (7.20%).