Here we report the fabrication of dye-doped polymer-stabilized liquid crystals (PSLC)-based smart windows. The effect of dye doping on PSLC contrast was investigated. Non-dichroic dye tints the PSLC sample in both off- and on-state, which is not beneficial for increasing its off/on contrast. The sample doped with dichroic dye shows a slight color in the off-state and strong color in the on-state, resulting in an enhanced contrast, which attributed to orientation dependent absorption of dichroic dyes. Furthermore, we blended non-dichroic dye and dichroic dye who have complementary absorption together into PSLC mixture. The sample is almost colorless in the off-state due to the subtractive process, while colored in the on-state. The contrast is further enhanced. The results show that the proposed multi-dye-doped PSLC device has high visual contrast and fast response time, making it attractive for applications in light management and architectural aesthetics.

Simultaneously achieving high efficiency and high durability in perovskite solar cells is a critical step toward the commercialization of this technology. Inverted perovskite photovoltaic (IP‐PV) cells incorporating robust and low levelized‐cost‐of‐energy (LCOE) buffer layers are supposed to be a promising solution to this target. However, insufficient inventory of materials for back‐electrode buffers substantially limits the development of IP‐PV. Herein, a composite consisting of 1D cation‐doped TiO₂ brookite nanorod (NR) embedded by 0D fullerene is investigated as a top modification buffer for IP‐PV. The cathode buffer is constructed by introducing fullerene to fill the interstitial space of the TiO₂ NR matrix. Meanwhile, cations of transition metal Co or Fe are doped into the TiO₂ NR to further tune the electronic property. Such a top buffer exhibits multifold advantages, including improved film uniformity, enhanced electron extraction and transfer ability, better energy level matching with perovskite, and stronger moisture resistance. Correspondingly, the resultant IP‐PV displays an efficiency exceeding 22% with a 22‐fold prolonged working lifetime. The strategy not only provides an essential addition to the material inventory for top electron buffers by introducing the 0D:1D composite concept, but also opens a new avenue to optimize perovskite PVs with desirable properties.