Perovskite photovoltachromic cells for building integration

Energy and Environmental Science Royal Society of Chemistry 8:5 (2015) 1578-1584

Authors:

Alessandro Cannavale, Giles Eperon, Pierluigi Cossari, Antonio Abate, Henry J Snaith, Giuseppe Gigli

Abstract:

Photovoltachromic devices combine photovoltaic and electrochromic behaviours to enable adjustable transparency glazing, where the photovoltaic component supplies the power to drive the coloration. Such stand-alone, self-powered devices are of commercial interest for integration into windows and surfaces of buildings and vehicles. Here, we report for the first time a perovskite-based photovoltachromic device with self-adaptive transparency. This multifunctional device is capable of producing electrical power by solar energy conversion as well as undergoing a chromic transition from neutral-color semi-transparent to dark blue-tinted when irradiated with solar light, without any additional external bias. The combination of semi-transparent perovskite photovoltaic and solid-state electrochromic cells enables fully solid-state photovoltachromic devices with 26% (or 16%) average visible transmittance and 3.7% (or 5.5%) maximum light power conversion efficiency. Upon activating the self-tinting, the average visible transmittance drops to 8.4% (or 5.5%). These results represent a significant step towards the commercialization of photovoltachromic building envelopes.

Efficiency Enhancement of Gallium Arsenide Photovoltaics Using Solution‐Processed Zinc Oxide Nanoparticle Light Scattering Layers

Journal of Nanomaterials Wiley 2015:1 (2015)

Authors:

Yangsen Kang, Dong Liang, Saahil Mehra, Yijie Huo, Yusi Chen, Mark G Christoforo, Alberto Salleo, James S Harris

Hole-transport materials with greatly-differing redox potentials give efficient TiO2-[CH3NH3][PbX3] perovskite solar cells.

Physical chemistry chemical physics : PCCP 17:4 (2015) 2335-2338

Authors:

Antonio Abate, Miquel Planells, Derek J Hollman, Vishal Barthi, Suresh Chand, Henry J Snaith, Neil Robertson

Abstract:

Two diacetylide-triphenylamine hole-transport materials (HTM) with varying redox potential have been applied in planar junction TiO2-[CH3NH3]PbI3-xClx solar cells leading to high power-conversion efficiencies up to 8.8%. More positive oxidation potential of the HTM gives higher VOC and lower JSC illustrating the role of matching energy levels, however both HTMs gave efficient cells despite a difference of 0.44 V in their redox potentials.

Optical Description of Mesostructured Organic-Inorganic Halide Perovskite Solar Cells.

The journal of physical chemistry letters 6:1 (2015) 48-53

Authors:

Miguel Anaya, Gabriel Lozano, Mauricio E Calvo, Wei Zhang, Michael B Johnston, Henry J Snaith, Hernán Míguez

Abstract:

Herein we describe both theoretically and experimentally the optical response of solution-processed organic-inorganic halide perovskite solar cells based on mesostructured scaffolds. We develop a rigorous theoretical model using a method based on the propagation of waves in layered media, which allows visualizing the way in which light is spatially distributed across the device and serves to quantify the fraction of light absorbed by each medium comprising the cell. The discrimination between productive and parasitic absorption yields an accurate determination of the internal quantum efficiency. State-of-the-art devices integrating mesoporous scaffolds infiltrated with perovskite are manufactured and characterized to support the calculations. This combined experimental and theoretical analysis provides a rational understanding of the optical behavior of perovskite cells and can be beneficial for the judicious design of devices with improved performance. Notably, our model justifies the presence of a solid perovskite capping layer in all of the highest efficiency perovskite solar cells based on thinner mesoporous scaffolds.

The real TiO2/HTM interface of solid-state dye solar cells: role of trapped states from a multiscale modelling perspective.

Nanoscale 7:3 (2015) 1136-1144

Authors:

Alessio Gagliardi, Matthias Auf der Maur, Desiree Gentilini, Fabio di Fonzo, Agnese Abrusci, Henry J Snaith, Giorgio Divitini, Caterina Ducati, Aldo Di Carlo

Abstract:

In this paper we present a multiscale simulation of charge transport in a solid-state dye-sensitized solar cell, where the real morphology between TiO2 and the hole transport material is included. The geometry of the interface is obtained from an electron tomography measurement and imported in a simulation software. Charge distribution, electric field and current densities are computed using the drift-diffusion model. We use this approach to investigate the electrostatic effect of trap states at the interface between the electron and hole transport materials. The simulations show that when the trapped electrons are not screened by external additives, the dynamics of holes is perturbed. Holes accumulate at the interface, enhancing recombination and reducing cell performance.