Methylammonium lead halide perovskite-based solar cells have demonstrated efficiencies as high as 24.2 %, highlighting their potential as inexpensive and solution-processable alternatives to silicon solar cell technologies.P oor stability towards moisture,u ltraviolet irradiation, heat, and ab ias voltage of the perovskite layer and its various device interfaces limits the commercial feasibility of this material for outdoor applications.Herein, we investigate the role of hydrogen bonding interactions induced when metal halide perovskite crystals are crosslinked with alkyl or p-conjugated boronic acid small molecules (-B(OH) 2 ). The crosslinked perovskite crystals are investigated under continuous light irradiation and moisture exposure.These studies demonstrate that the origin of the interaction between the alkylorp-conjugated crosslinking molecules is due to hydrogen bonding between the -B(OH) 2 terminal group of the crosslinker and the Io ft he [PbI 6 ] 4À octahedra of the perovskite layer.A lso,t his interaction influences the stability of the perovskite layer towards moisture and ultraviolet light irradiation. Morphology and structural analyses,aswell as IR studies as afunction of aging under both dark and light conditions showthat p-conjugated boronic acid molecules are more effective crosslinkers of the perovskite crystals than their alkylc ounterparts thus imparting better stability towards light and moisture degradation.