In principle, the induced chirality of hybrid perovskites results from symmetry-breaking within inorganic frameworks. However, the detailed mechanism behind the chirality transfer remains unknown due to the lack of systematic studies. Here, using the structural isomer with different functional group location, we deduce the effect of hydrogen-bonding interaction between two building blocks on the degree of chirality transfer in inorganic frameworks. The effect of asymmetric hydrogen-bonding interaction on chirality transfer was clearly demonstrated by thorough experimental analysis. Systematic studies of crystallography parameters confirm that the different asymmetric hydrogen-bonding interactions derived from different functional group location play a key role in chirality transfer phenomena and the resulting spin-related properties of chiral perovskites. The methodology to control the asymmetry of hydrogen-bonding interaction through the small structural difference of structure isomer cation can provide rational design paradigm for unprecedented spin-related properties of chiral perovskite.

Due to their intrinsic spin control capability and excellent catalytic activity, chiral inorganic materials have been recognized as promising candidates for achieving a breakthrough in the solar-to-hydrogen efficiency of water-splitting...

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Correction for ‘Elucidating the chirality transfer mechanisms during enantioselective synthesis for the spin-controlled oxygen evolution reaction’ by Hayoung Im et al., Energy Environ. Sci., 2023, 16, 1187–1199, https://doi.org/10.1039/D2EE03853F.

To realize practical solar hydrogen production, a low‐cost photocathode with high photocurrent density and onset potential should be developed. Herein, an efficient and stable overall photoelectrochemical tandem cell is developed with a Cu3BiS3‐based photocathode. By exploiting the crystallographic similarities between Bi2S3 and Cu3BiS3, a one‐step solution process with two sulfur sources is used to prepare the Bi2S3–Cu3BiS3 blended interlayer. The elongated Bi2S3‐Cu3BiS3 mixed‐phase 1D nanorods atop a planar Cu3BiS3 film enable a high photocurrent density of 7.8 mA cm−2 at 0 V versus the reversible hydrogen electrode, with an onset potential of 0.9 VRHE. The increased performance over the single‐phase Cu3BiS3 thin‐film photocathode is attributed to the enhanced light scattering and charge collection through the unique 1D nanostructure, improved electrical conductivity, and better band alignment with the n‐type CdS layer. A solar‐to‐hydrogen efficiency of 2.33% is achieved under unassisted conditions with a state‐of‐the‐art Mo:BiVO4 photoanode, with excellent stability exceeding 21 h.