than that of the holes in CH 3 NH 3 PbCl 3− x I x ( L eff, e− / L eff , h+ < 1), measured by the electron-beam induced current (EBIC) method, [ 23 ] a mesoporous electron transporting scaffold is indispensable to effectively extract and transport the electrons. Consequently, high PCEs over 15% from meso-superstructured pero-HSCs (MS pero-HSCs) have been achieved by applying mesoporous TiO 2 and Al 2 O 3 as the electron extraction layer (EEL) and insulating scaffold, respectively. [24][25][26][27][28] In addition, one outstanding advantage of MS pero-HSCs over that of PHJ pero-HSCs is the higher consistence of effi ciency under different scan rates and scan directions, showing less hysteresis and transient behavior in current-voltage measurement, [ 29 ] which is critically important for high throughput large-scale manufacturing pero-HSCs products. Nevertheless, the high temperature sintering process for mesoporous metal oxides (TiO 2 /Al 2 O 3 ) and the homogeneous infi ltration of perovskite materials into the mesoporous electron extraction material [24][25][26][27][28] are especially adverse for large-scale commercialization of pero-HSCs.To address these problems, we fabricate conventional "bulk heterojunction" (BHJ) pero-HSCs by mixing PC 61 BM ([6,6]-phenyl-C61-butyric acid methyl ester) with CH 3 NH 3 PbI 3 , which aims to circumvent issues existed in the PHJ and MS pero-HSCs, while inheriting advantages from both constructions. In the conventional BHJ pero-HSCs, PC 61 BM has twofold contributions. First, PC 61 BM can effectively extract the electrons from the PC 61 BM/CH 3 NH 3 PbI 3 interfaces, [ 30,31 ] which is originated from the high electron affi nity (−4.3 eV) of PC 61 BM [ 32 ] and a ≈0.4 eV energy level offset between the lowest unoccupied molecular orbit (LUMO) energy level of CH 3 NH 3 PbI 3 (−3.9 eV) and that of PC 61 BM (−4.3 eV). In this way, PC 61 BM acts as the "electron acceptor" in the BHJ composite of CH 3 NH 3 PbI 3 :PC 61 BM, which would address the issues induced by the shorter diffusion length of the electrons than that of holes in CH 3 NH 3 PbI 3 .[ 23 ] Second, a retarded reaction between CH 3 NH 3 I and PbI 2 is expected with the addition of PC 61 BM. The interactions between the ester group of PC 61 BM and CH 3 NH 3 I could form an intermediate phase, which is expected to induce more uniform and dense perovskite layers (detailed discussion in later context).