Prof Henry Snaith FRS

Abstract:

The solid-state dye-sensitized solar cell (DSSC) was introduced to overcome inherent manufacturing and instability issues of the electrolyte-based DSSC and progress has been made to deliver high photovoltaic efficiencies at low cost. However, despite 15 years research and development, there still remains no clear demonstration of long-term stability. Here, solid-state DSSCs are subjected to the severe aging conditions of continuous illumination at an elevated temperature. A fast deterioration in performance is observed for devices encapsulated in the absence of oxygen. The photovoltaic performance recovers when re-exposed to air. This reversible behavior is attributed to three related processes: i) the creation of light and oxygen sensitive electronic shunting paths between TiO2 and the top metal electrode, ii) increased recombination at the TiO2/organic interface, and iii) the creation of deep electron traps that reduce the photocurrent. The device deterioration is remedied by the formation of an insulating alumino-silicate shell around the TiO2 nanocrystals, which reduces interfacial recombination, and the introduction of an insulating mesoporous SiO2 buffer layer between the top electrode and TiO2, which acts as a permanent insulating barrier between the TiO2 and the metal electrode, preventing shunting. Encapsulated solid-state dye-sensitized solar cells (ssDSSCs) show a reversible and quick deterioration in performance while aging under inert atmosphere. This is attributed to the activation of deep traps and the change in Schottky barrier at the TiO2 surface. This is remedied by forming an insulating alumino-silicate "shell" around the TiO2 nanocrystals, and by introducing an insulating mesoporous SiO2 "buffer layer" between the top electrode and TiO2. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Abstract:

The field of solution-processed photovoltaic cells is currently in its second spring. The dye-sensitized solar cell is a widely studied and longstanding candidate for future energy generation. Recently, inorganic absorber-based devices have reached new record efficiencies, with the benefits of all-solid-state devices. In this rapidly changing environment, this review sheds light on recent developments in all-solid-state solar cells in terms of electrode architecture, alternative sensitizers, and hole-transporting materials. These concepts are of general applicability to many next-generation device platforms.

Abstract:

Organic-inorganic halide perovskites, such as CH3NH3PbX3 (X = I(-), Br(-), Cl(-)), are attracting growing interest to prepare low-cost solar cells that are capable of converting sunlight to electricity at the highest efficiencies. Despite negligible effort on enhancing materials' purity or passivation of surfaces, high efficiencies have already been achieved. Here, we show that trap states at the perovskite surface generate charge accumulation and consequent recombination losses in working solar cells. We identify that undercoordinated iodine ions within the perovskite structure are responsible and make use of supramolecular halogen bond complexation to successfully passivate these sites. Following this strategy, we demonstrate solar cells with maximum power conversion efficiency of 15.7% and stable power output over 15% under constant 0.81 V forward bias in simulated full sunlight. The surface passivation introduces an important direction for future progress in perovskite solar cells.

Abstract:

We determine high charge-carrier mobilities ≥ 33 cm2 V−1 s−1 and bi-molecular recombination rates about five orders of magnitude below the prediction of Langevin's model for vapour-deposited CH3NH3PbI3−xClx using ultrafast THz spectroscopy. At charge-carrier densities below ∼1017 cm−3 intrinsic diffusion lengths are shown to approach 3 microns, limited by slow mono-molecular decay processes.