Reducing non-radiative recombination and addressing band alignment mismatches at interfaces remain major challenges in achieving high-performance wide-bandgap perovskite solar cells. This study proposes the self-organization of a thin two-dimensional (2D) perovskite BAPbBr layer beneath a wide-bandgap three-dimensional (3D) perovskite CsFAPb(IBr), forming a 2D/3D bilayer structure on a tin oxide (SnO) layer. This process is driven by interactions between the oxygen vacancies on the SnO surface and hydrogen atoms of the n-butylammonium cation, aiding the self-assembly of the BAPbBr 2D layer. The 2D perovskite acts as a tunneling layer between SnO and the 3D perovskite, neutralizing the energy level mismatch and reducing non-radiative recombination. This results in high power conversion efficiencies of 21.54% and 19.16% for wide-bandgap perovskite solar cells with bandgaps of 1.7 and 1.8 eV, with open-circuit voltages over 1.3 V under 1-Sun illumination. Furthermore, an impressive efficiency of over 43% is achieved under indoor conditions, specifically under 200 lux white light-emitting diode light, yielding an output voltage exceeding 1 V. The device also demonstrates enhanced stability, lasting up to 1,200 hours.
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http://dx.doi.org/10.1002/adma.202402053 | DOI Listing |
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