Buried Interface Engineering Enables Efficient and 1,960-hour Isos-L-2i Stable Inverted Perovskite Solar Cells
Creators
- 1. Michael Grätzel Center for Mesoscopic Solar Cells, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, 430074 China
- 2. Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, École Polytechnique Fédéralede Lausanne (EPFL), CH-1015 Lausanne, Switzerland
- 3. Laboratory of Computational Chemistry and Biochemistry, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland
- 4. Michael Grätzel Center for MesoscopicSolar Cells, Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074,China
- 5. Laboratory of Computational Chemistry and Biochemistry, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, CH-1015 Switzerland
- 6. Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, CH-1015 Switzerland
- 7. School of Chemistry, Chemical Engineering, and Life Sciences, Wuhan University of Technology, Wuhan, 430070 China
Description
High-performance perovskite solar cells (PSCs) typically require interfacial passivation, yet this is challenging for the buried interface, owing to the dissolution of passivation agents during the deposition of perovskites. Here, we overcome this limitation with in-situ buried interface passivation – achieved via directly adding a cyanoacrylic acid-based molecular additive, namely BT-T, into the perovskite precursor solution. Classical and ab-initio molecular dynamics simulations reveal that BT-T spontaneously may self-assemble at the buried interface during the formation of the perovskite layer on a nickel oxide hole transporting layer. The preferential buried interface passivation results in facilitated hole transfer and suppressed charge recombination. In addition, residual BT-T molecules in the perovskite layer enhance its stability and homogeneity. We report a power-conversion efficiency (PCE) of 23.48% for 1.0 cm2 inverted-structure PSCs. The encapsulated PSC retains 95.4% of its initial PCE following 1,960-hour maximum power point tracking under continuous light illumination at 65°C (i.e., ISOS-L-2I protocol). Our demonstration of operating-stable PSCs under accelerated ageing conditions represents a step closer to the commercialization of this emerging technology.
Notes
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Additional details
Related works
- Is cited by
- Journal article: 10.1002/adma.202303869 (DOI)
Funding
- NCCR MUST: Molecular Ultrafast Science and Technology (phase III) 51NF40-183615
- Swiss National Science Foundation
- Next-Generation Multiscale Molecular Dynamics: Promoting Computational Chemistry with Artificial Intelligence 200020_185092
- Swiss National Science Foundation