nanostructured α-Fe 2 O 3 exhibits more size-dependent properties induced by the high surface area and quantum confinement. [5][6][7][8] Assembly of α-Fe 2 O 3 nanoparticles (NPs) into periodic arrays has attracted high attention due to their potential applications in photoelectrochemical conversion, [9,10] photovoltaic devices, [11][12][13][14] lithium-ion batteries, [4,7,8,[15][16][17] gas sensors, [6,18,19] and high-density nanoelectronic technologies. [20,21] Here the morphology is of particular relevance. For example, when used as the electron transport layer for photovoltaic devices, the nanoscale morphology will affect the charge carrier transport and thereby the device efficiency. [22] Current lithographic techniques employed in the microelectronic industry face the escalating production cost by further decreasing the feature size. [23][24][25] As an inexpensive alternative, the block copolymer templated sol-gel method can achieve various nanoscale structures with the assistance of selfassembly of block copolymers. [2,20,[26][27][28][29][30] Typically, nanopatterning of the Fe 2 O 3 NPs through block copolymer templates can be categorized into two types: directly accommodating the NPs inside the block copolymer matrix or in situ reducing block copolymer coordinated metal precursors into NPs. To accommodate the NPs, a special surface treatment of the NPs Mesoporous α-Fe 2 O 3 thin films with large area homogeneity demonstrate tremendous potential in multiple applications. In the present work, the synthesis of morphology-controlled α-Fe 2 O 3 thin films is realized with polystyrene-blockpoly(4-vinyl pyridine) (PS-b-P 4 VP) diblock copolymer assisted sol-gel chemistry. The solvent category (DMF and 1,4-dioxane) and polymer-to-FeCl 3 ratio used for the solution preparation are systematically varied to tune the morphology of the thin films. For both solvents, DMF and 1,4-dioxane, nanocluster structures are obtained with low PS-b-P 4 VP concentration. When the concentration of PS-b-P 4 VP reaches the critical micelle concentration, spherical and wormlike porous structures are specifically formed in the DMF and 1,4-dioxane solvent system, respectively. Further increasing the polymer-to-FeCl 3 ratios leads to the enlargement of the spherical pore sizes in the DMF system, whereas the center-to-center distances of the wormlike structures in the 1,4-dioxane system decrease. Moreover, DMF/1,4-dioxane solvent mixtures with different volume ratios are applied for the sol-gel solution preparation to gain more insight into how the solvent selectivity affects the thin film morphology. By adjusting the preferential affinity of the solvent mixture to the polymer blocks, a spherical to wormlike pore shape transition is observed with a critical Δχ value of around 0.77.