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CMP
Credit: Jack Hobhouse

Prof Henry Snaith FRS

Professor of Physics

Sub department

  • Condensed Matter Physics

Research groups

  • Snaith group
  • Advanced Device Concepts for Next-Generation Photovoltaics
Henry.Snaith@physics.ox.ac.uk
Robert Hooke Building, room G21
  • About
  • Publications

Perovskite Crystals for Tunable White Light Emission

Chemistry of Materials American Chemical Society (ACS) 27:23 (2015) 8066-8075

Authors:

Sandeep Pathak, Nobuya Sakai, Florencia Wisnivesky Rocca Rivarola, Samuel D Stranks, Jiewei Liu, Giles E Eperon, Caterina Ducati, Konrad Wojciechowski, James T Griffiths, Amir Abbas Haghighirad, Alba Pellaroque, Richard H Friend, Henry J Snaith
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A mixed-cation lead mixed-halide perovskite absorber for tandem solar cells

Science American Association for the Advancement of Science 351:6269 (2015) 151-155

Authors:

Amir A Haghighirad, David P McMeekin, Golnaz Sadoughi, Waqaas Rehman, Giles E Eperon, Michael Saliba, Maximilian T Horanter, Nobuya Sakai, Lars Korte, Bernd Rech, Michael B Johnston, Laura M Herz, Henry J Snaith

Abstract:

Metal halide perovskite photovoltaic cells could potentially boost the efficiency of commercial silicon photovoltaic modules from ∼20 toward 30% when used in tandem architectures. An optimum perovskite cell optical band gap of ~1.75 electron volts (eV) can be achieved by varying halide composition, but to date, such materials have had poor photostability and thermal stability. Here we present a highly crystalline and compositionally photostable material, [HC(NH2)2](0.83)Cs(0.17)Pb(I(0.6)Br(0.4))3, with an optical band gap of ~1.74 eV, and we fabricated perovskite cells that reached open-circuit voltages of 1.2 volts and power conversion efficiency of over 17% on small areas and 14.7% on 0.715 cm(2) cells. By combining these perovskite cells with a 19%-efficient silicon cell, we demonstrated the feasibility of achieving >25%-efficient four-terminal tandem cells.
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Structured organic–inorganic perovskite toward a distributed feedback laser

Advanced Materials Wiley 28:5 (2015) 923-929

Authors:

Michael Saliba, Simon Wood, Jay Patel, Pabitra Nayak, Jian Huang, Jack Alexander-Webber, Bernard Wenger, Samuel Stranks, Maximilian Hörantner, Jacob Wang, Robin Nicholas, Laura Herz, Michael Johnston, Stephen Morris, Henry Snaith, Moritz Riede

Abstract:

A general strategy for the in-plane structuring of organic-inorganic perovskite films is presented. The method is used to fabricate an industrially relevant distributed feedback (DFB) cavity, which is a critical step towards all-electrially pumped injection laser diodes. This approach opens the prospects of perovskite materials for much improved optical control in LEDs, solar cells and also toward applications as optical devices.
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Modulating the Electron-Hole Interaction in a Hybrid Lead Halide Perovskite with an Electric Field.

Journal of the American Chemical Society 137:49 (2015) 15451-15459

Authors:

Tomas Leijtens, Ajay Ram Srimath Kandada, Giles E Eperon, Giulia Grancini, Valerio D'Innocenzo, James M Ball, Samuel D Stranks, Henry J Snaith, Annamaria Petrozza

Abstract:

Despite rapid developments in both photovoltaic and light-emitting device performance, the understanding of the optoelectronic properties of hybrid lead halide perovskites is still incomplete. In particular, the polarizability of the material, the presence of molecular dipoles, and their influence on the dynamics of the photoexcitations remain an open issue to be clarified. Here, we investigate the effect of an applied external electric field on the photoexcited species of CH3NH3PbI3 thin films, both at room temperature and at low temperature, by monitoring the photoluminescence (PL) yield and PL decays. At room temperature we find evidence for electric-field-induced reduction of radiative bimolecular carrier recombination together with motion of charged defects that affects the nonradiative decay rate of the photoexcited species. At low temperature (190 K), we observe a field-induced enhancement of radiative free carrier recombination rates that lasts even after the removal of the field. We assign this to field-induced alignment of the molecular dipoles, which reduces the vibrational freedom of the lattice and the associated local screening and hence results in a stronger electron-hole interaction.
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Enhanced optoelectronic quality of perovskite thin films with hypophosphorous acid for planar heterojunction solar cells

(2015)

Authors:

W Zhang, S Pathak, N Sakai, T Stergiopoulos, PK Nayak, NK Noel, AA Haghighirad, VM Burlakov, DW deQuilettes, A Sadhanala, W Li, L Wang, DS Ginger, RH Friend, Henry Snaith

Abstract:

Solution-processed metal halide perovskite semiconductors, such as CH3NH3PbI3, have exhibited remarkable performance in solar cells, despite having non-negligible density of defect states. A likely candidate is halide vacancies within the perovskite crystals, or the presence of metallic lead, both generated due to the imbalanced I/Pb stoichiometry which could evolve during crystallization. Herein, we show that the addition of hypophosphorous acid (HPA) in the precursor solution can significantly improve the film quality, both electronically and topologically, and enhance the photoluminescence intensity, which leads to more efficient and reproducible photovoltaic devices. We demonstrate that the HPA can reduce the oxidized I2 back into I(-), and our results indicate that this facilitates an improved stoichiometry in the perovskite crystal and a reduced density of metallic lead.
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