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Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Boosting perovskite nanomorphology and charge transport properties via a functional D-π-A organic layer at the
Mohamed M Elsenety1, Anastasios Stergiou2, Labrini Sygellou3
1National Centre for Scientific Research "Demokritos", Institute of Nanoscience and Nanotechnology, 15341, Agia Paraskevi Attikis, Athens, Greece. p.falaras@inn.demokritos.gr.
Abstract:
The photovoltaic efficiency and stability challenges encountered in perovskite solar cells (PSCs) were addressed by an innovative interface engineering approach involving the utilization of the organic chromophore (E)-3-(5-(4-(bis(2',4'-dibutoxy-[1,1'-biphenyl]-4-yl)amino)phenyl)thiophen-2-yl)-2-cyanoacrylic acid (D35) as an interlayer between the perovskite absorber and the hole transporter (HTM) of mesoporous PSCs. The organic D-π-A interlayer primarily improves the perovskite's crystallinity and creates a smoother perovskite/HTM interface, while reducing the grain boundary defects and inducing an energy level alignment with the adjacent layers. Champion power conversion efficiencies (PCE) as high as 18.5% were obtained, clearly outperforming the reference devices. Interestingly, the D35-based solar cells present superior stability since they preserved 83% of their initial efficiency after 37 days of storage under dark and open circuit (OC) conditions. The obtained results consolidate the multifunctional role of organic D-π-A molecules as perovskite interface modifiers towards performance enhancement and scale-up fabrication of robust PSCs.

