Prof. Anders Hagfeldt Profile

Prof. Anders Hagfeldt

at Uppsala Univ

SPIE Involvement:

Author

Publications (5)

Proceedings Article | 1 August 2021 Presentation

Nanoscale interfacial engineering enables highly stable and efficient perovskite photovoltaics

Anurag Krishna, Hong Zhang, Zhiwen Zhou, Thibaut Gallet, Mathias Dankl, Olivier Ouellette, Felix Eickemeyer, Fan Fu, Mounir Mensi, Shaik Zakeeruddin, Ursula Rothlisberger, G. N. Manjunatha Reddy, Alex Redinger, Michael Grätzel, Anders Hagfeldt

Proceedings Volume 11809, 118090O (2021) https://doi.org/10.1117/12.2597193

KEYWORDS: Perovskite, Photovoltaics, Solar cells, Interfaces, Sun, Molecular interactions, Modulation, Lead, Ions, Chemical analysis

Read Abstract +

Proceedings Article | 23 August 1995 Paper

Charge separation and charge transport in nanostructured TiO2 film electrodes

Henrik Lindstrom, Anders Hagfeldt, Hakan Rensmo, Anita Solbrand, Sven Sodergren, Sten-Eric Lindquist

Proceedings Volume 2531, (1995) https://doi.org/10.1117/12.217355

KEYWORDS: Electrodes, Electrons, Particles, Interfaces, Semiconductors, Absorption, Oxygen, Glasses, Nanostructuring, Quantum efficiency

Read Abstract +

Photoelectrochemical measurements have been performed on film electrodes consisting of linked nano-sized TiO₂ colloids. The film thickness ranged from 1 - 40 micrometers. The film network was attached to a thin transparent conducting layer of SnO₂ allowing for photogenerated electrons to be collected in an outer electrical circuit. By illuminating electrodes of different thicknesses with monochromatic light from either side, it was possible to induce charge separation in different regions of the film network. In this way, it was proved that electrons have different probabilities of reaching the back contact depending on the location in the film where they are created. The results also illustrate the importance of the redox species in the cavities of these porous electrodes. By adding acceptors to the electrolyte it was possible to alter the conditions for charge transfer in the nanocrystalline film. It was shown that electron acceptors such as oxygen or iodine in the solution strongly affects the rate of charge transfer at the particle-electrolyte interface and the transport of electrons throughout the TiO₂ film-network. Modification of the semiconductor-electrolyte interface with surface adsorbed pyridine induced major changes in the charge transfer events at the interface. The photocurrent yields were greatly improved by this surface treatment. The effect of pH in solution was also investigated. The rate of charge transfer at the particle-electrolyte interface was changed at high surface density of OH^--ions. This was explained due to the change of the surface energy causing different driving forces for redox reactions, but also due to the more negatively electrostatic surface potential of the particles preventing the encounter of negatively charged redox species with the colloid surface. Phototransient measurements indicated a depletion of redox species in the pores of the film. Thereby it was pointed out that the dynamics of the redox species in the confined cavities of the film are a limiting factor for the charge separation efficiency in nanocrystalline film. The photovoltage in anaerobic solutions sustained for very long periods, indicating that the linked particles may work as reservoirs for photoexcited electrons if the access to electron acceptors in the solution is choked. It was concluded that surface processes are favored at the small semiconductor particles used in this study.