Confinement and passivation of perovskite quantum dots in porous natural palygorskite toward an efficient and ultrastable light-harvesting system in water

Perovskite quantum dots (QDs) are promising as representative candidates to construct next-generation superior artificial light-harvesting systems (ALHSs). However, their high sensitivity to external environments, especially to water, imposes a stringent limitation for their actual implementation. Herein, by interface engineering and encapsulation with natural palygorskite (PAL), a water-resistant light-harvesting CsPbBr3@PAL antenna was prepared. Molecular dynamics simulations further confirm a significant shielding protection of the PAL matrix to CsPbBr3, facilitating exceptional stability of the CsPbBr3@PAL antenna when exposed to air for 10 months, to 150 degrees C thermal stress, and even to water for more than 30 days, respectively. Furthermore, as a result of in situ encapsulation of the PAL matrix and defect passivation caused by H-bonding and coordination-bonding interaction, the CsPbBr3@PAL antenna in water shows a substantially enhanced photoluminescence quantum yield (36.2%) and longer lifetime. After sequentially assembling Eosin Y and Rose Bengal in the pores of the PAL matrix, RB-ESY-CsPbBr3@PAL with a sequential two-step efficient Forster resonance energy transfer process exhibited extremely enhanced photocatalytic activity toward Friedel-Crafts alkylation reactions in aqueous solution, 2.5-fold higher than that of corresponding ESY/RB. Our work provides a feasible strategy for the exploitation of ultra-stable halide perovskite-based ALHSs in aqueous media for solar-energy conversion.