Journal
JOURNAL OF MATERIALS CHEMISTRY C
Volume 5, Issue 35, Pages 9037-9043Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7tc02954c
Keywords
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Funding
- National Natural Science Foundation of China [11374168, 51302137]
- K. C. Wong Magna Fund in Ningbo University of China
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Morphology and crystallinity of perovskite layers are crucial for power conversion efficiency (PCE) of perovskite solar cells (PSCs). Here, we introduced amorphous polymer polyvinylpyrrolidone (PVP) with a C=O functional group into a CH3NH3PbI3-xClx perovskite precursor to tune the morphology and crystallinity of perovskite layers during the film formation process. The spreading amorphous polymer chains and excellent hygroscopicity of PVP can help the perovskite precursor have better contact with the substrate, leading to better perovskite film coverage. More importantly, the electron pair existing in the oxygen atom of the C=O bond in PVP has a strong attraction to Pb(II) ions, which can adjust the location of the nuclei and make the nuclei distribute uniformly in PVP chains, contributing to a uniform and compact perovskite layer. As a result, perovskite films with PVP present favourable morphology and improved crystallinity. The performance of a CH3NH3PbI3-xClx-based perovskite solar cell with optimized PVP content achieves a summit PCE of 16.57% with photovoltage V-OC of 1057 mV, short circuit current density J(SC) of 21.38 mA cm(-2), and fill factor FF of 74.52% under standard AM 1.5 solar light of 100 mW cm(-2) intensities, which demonstrates a 23.9% increment compared with a PCE of 13.37% of the original device.
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