“…The high activity is ascribed to the unique complex hollow structure, broad light absorption range from ultraviolet light–responsive ZnS and visible light–responsive CdS, and promoted charge separation in the heterostructure (Figure H,I). In another work, a sequential templating approach was performed to fabricate heterostructured TiO 2 /Fe 2 TiO 5 photocatalysts with tunable Fe/Ti molar ratios and controllable single‐, double‐, triple‐, core‐, and closed‐double‐shelled structures . Among all these photocatalysts, the closed‐double‐shelled sample manifests the highest activity with the O 2 evolution rate of 375 µmol g −1 h −1 and good stability for 5 h. The abundant active sites, promoted light absorption, reduced charge transfer distance, and enhanced charge separation derived from the multishelled heterostructure are believed to be the reasons for the high activity.…”