Phosphonic anchoring groups in organic dyes for solid-state solar cells.

Physical chemistry chemical physics : PCCP 17:28 (2015) 18780-18789

Authors:

Antonio Abate, Raquel Pérez-Tejada, Konrad Wojciechowski, Jamie M Foster, Aditya Sadhanala, Ullrich Steiner, Henry J Snaith, Santiago Franco, Jesús Orduna

Abstract:

We report the synthesis and the optoelectronic characterization of three new 4H-pyran-4-ylidene and thiazole derivatives (pyt) as metal-free organic dyes for solid-state dye-sensitized solar cells (DSSCs). We investigate the performance and the long-term stability of devices employing pyt dyes functionalized with carboxylic and phosphonic acids as TiO2 anchoring groups. In contrast to reports on liquid electrolyte DSSCs, we show that solid-state DSSCs prepared with phosphoric pyt derivatives can achieve similar power conversion efficiency to their carboxyl analogues. We make use of the Mott-Schottky analysis and equivalent circuit models to demonstrate that a phosphonic group induces a significant increase in built-in voltage at the TiO2-hole transporter interface, which results in a higher open circuit voltage.

Novel Low Cost Hole Transporting Materials for Efficient Organic-Inorganic Perovskite Solar Cells

Institute of Electrical and Electronics Engineers (IEEE) (2015) 1-4

Authors:

Jiewei Liu, Sandeep Pathak, Tomas Leijtens, Thomas Stergiopoulos, Konrad Wojciechowski, Stefan Schumann, Nina Kausch-Busies, Henry J Snaithl

C60 as an Efficient n-Type Compact Layer in Perovskite Solar Cells.

The journal of physical chemistry letters 6:12 (2015) 2399-2405

Authors:

Konrad Wojciechowski, Tomas Leijtens, Svetlana Siprova, Christoph Schlueter, Maximilian T Hörantner, Jacob Tse-Wei Wang, Chang-Zhi Li, Alex K-Y Jen, Tien-Lin Lee, Henry J Snaith

Abstract:

Organic-inorganic halide perovskite solar cells have rapidly evolved over the last 3 years. There are still a number of issues and open questions related to the perovskite material, such as the phenomenon of anomalous hysteresis in current-voltage characteristics and long-term stability of the devices. In this work, we focus on the electron selective contact in the perovskite solar cells and physical processes occurring at that heterojunction. We developed efficient devices by replacing the commonly employed TiO2 compact layer with fullerene C60 in a regular n-i-p architecture. Detailed spectroscopic characterization allows us to present further insight into the nature of photocurrent hysteresis and charge extraction limitations arising at the n-type contact in a standard device. Furthermore, we show preliminary stability data of perovskite solar cells under working conditions, suggesting that an n-type organic charge collection layer can increase the long-term performance.

Observation and Mediation of the Presence of Metallic Lead in Organic-Inorganic Perovskite Films.

ACS applied materials & interfaces 7:24 (2015) 13440-13444

Authors:

Golnaz Sadoughi, David E Starr, Evelyn Handick, Samuel D Stranks, Mihaela Gorgoi, Regan G Wilks, Marcus Bär, Henry J Snaith

Abstract:

We have employed soft and hard X-ray photoelectron spectroscopies to study the depth-dependent chemical composition of mixed-halide perovskite thin films used in high-performance solar cells. We detect substantial amounts of metallic lead in the perovskite films, which correlate with significant density of states above the valence band maximum. The metallic lead content is higher in the bulk of the perovskite films than at the surface. Using an optimized postanneal process in air, we can reduce the metallic lead content in the perovskite film. This process reduces the amount of metallic lead and a corresponding increase in the photoluminescence quantum efficiency of the perovskite films can be observed. This correlation indicates that metallic lead impurities are likely a key defect whose concentration can be controlled by simple annealing procedures in order to increase the performance for perovskite solar cells.

Enhanced Amplified Spontaneous Emission in Perovskites using a Flexible Cholesteric Liquid Crystal Reflector

Nano letters American Chemical Society 15:8 (2015) 4935-4941

Authors:

Samuel D Stranks, Simon M Wood, Konrad Wojciechowski, Felix Deschler, Michael Saliba, Hitesh Khandelwal, Jay B Patel, Steve J Elston, Laura Herz, Michael Johnston, Albertus PHJ Schenning, Michael G Debije, Moritz Riede, Stephen M Morris, Henry J Snaith

Abstract:

Organic-inorganic perovskites are highly promising solar cell materials with laboratory-based power conversion efficiencies already matching those of established thin film technologies. Their exceptional photovoltaic performance is in part attributed to the presence of efficient radiative recombination pathways, thereby opening up the possibility of efficient light-emitting devices. Here, we demonstrate optically pumped amplified spontaneous emission (ASE) at 780 nm from a 50 nm-thick film of CH3NH3PbI3 perovskite that is sandwiched within a cavity composed of a thin-film (∼7 μm) cholesteric liquid crystal (CLC) reflector and a metal back-reflector. The threshold fluence for ASE in the perovskite film is reduced by at least two orders of magnitude in the presence of the CLC reflector, which results in a factor of two reduction in threshold fluence compared to previous reports. We consider this to be due to improved coupling of the oblique and out-of-plane modes that are reflected into the bulk in addition to any contributions from cavity modes. Furthermore, we also demonstrate enhanced ASE on flexible reflectors and discuss how improvements in the quality factor and reflectivity of the CLC layers could lead to single-mode lasing using CLC reflectors. Our work opens up the possibility of fabricating widely wavelength-tunable "mirror-less" single-mode lasers on flexible substrates, which could find use in applications such as flexible displays and friend or foe identification.