Abstract

Perovskite solar cells (PSCs) have demonstrated over 25% power conversion efficiency (PCE) via efficient surface passivation. Unfortunately, state-of-the-art perovskite post-treatment strategies can solely heal the top interface defects. Herein, we propose an ion diffusion management strategy to concurrently modulate the top interfaces, buried interfaces, and bulk interfaces (i.e., grain boundaries) of perovskite film, enabling all-interface defect passivation. Specifically, this method is enabled by applying double interactive salts of octylammonium iodide (OAI) and guanidinium chloride (GACl) onto the three-dimensional (3D) perovskite surface. We reveal that the hydrogen-bonding interaction between OA+ and GA+ decelerates the OA+ diffusion and therefore forms dimensionally broadened 2D capping layer. Additionally, the diffusion of GA+ and Cl- determines the composition of the bulk and buried interface of PSCs. As a result, we can obtain n-inter-i-inter-p, i.e., 5-layer structured PSCs with a champion PCE of 25.43% (certified 24.4%). This approach also enables the substantially improved operational stability of perovskite solar cells. This article is protected by copyright. All rights reserved.

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