TY  - JOUR
A1  - Cappel, Ute B.
A1  - Svanstrom, Sebastian
A1  - Lanzilotto, Valeria
A1  - Johansson, Fredrik O. L.
A1  - Aitola, Kerttu
A1  - Philippe, Bertrand
A1  - Giangrisostomi, Erika
A1  - Ovsyannikov, Ruslan
A1  - Leitner, Torsten
A1  - Föhlisch, Alexander
A1  - Svensson, Svante
A1  - Martensson, Nils
A1  - Boschloo, Gerrit
A1  - Lindblad, Andreas
A1  - Rensmo, Hakan
T1  - Partially Reversible Photoinduced Chemical Changes in a Mixed-Ion Perovskite Material for Solar Cells
JF  - ACS applied materials & interfaces
N2  - Metal halide perovskites have emerged as materials of high interest for solar energy-to-electricity conversion, and in particular, the use of mixed-ion structures has led to high power conversion efficiencies and improved stability. For this reason, it is important to develop means to obtain atomic level understanding of the photoinduced behavior of these materials including processes such as photoinduced phase separation and ion migration. In this paper, we implement a new methodology combining visible laser illumination of a mixed-ion perovskite ((FAP-bI(3))(0.85)(MAPbBr(3))(0.15)) with the element specificity and chemical sensitivity of core-level photoelectron spectroscopy. By carrying out measurements at a synchrotron beamline optimized for low X-ray fluxes, we are able to avoid sample changes due to X-ray illumination and are therefore able to monitor what sample changes are induced by visible illumination only. We find that laser illumination causes partially reversible chemistry in the surface region, including enrichment of bromide at the surface, which could be related to a phase separation into bromide- and iodide-rich phases. We also observe a partially reversible formation of metallic lead in the perovskite structure. These processes occur on the time scale of minutes during illumination. The presented methodology has a large potential for understanding light-induced chemistry in photoactive materials and could specifically be extended to systematically study the impact of morphology and composition on the photostability of metal halide perovskites.
KW  - photoelectron spectroscopy
KW  - laser illumination
KW  - lead halide perovskite
KW  - ion migration
KW  - phase separation
KW  - stability
Y1  - 2017
U6  - https://doi.org/10.1021/acsami.7b10643
SN  - 1944-8244
VL  - 9
SP  - 34970
EP  - 34978
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Sorgenfrei, Nomi
A1  - Giangrisostomi, Erika
A1  - Jay, Raphael Martin
A1  - Kühn, Danilo
A1  - Neppl, Stefan
A1  - Ovsyannikov, Ruslan
A1  - Sezen, Hikmet
A1  - Svensson, Svante
A1  - Föhlisch, Alexander
T1  - Photodriven transient picosecond top-layer semiconductor to metal phase-transition in p-doped molybdenum disulfide
JF  - Advanced materials
N2  - Visible light is shown to create a transient metallic S-Mo-S surface layer on bulk semiconducting p-doped indirect-bandgap 2H-MoS2. Optically created electron-hole pairs separate in the surface band bending region of the p-doped semiconducting crystal causing a transient accumulation of electrons in the surface region. This triggers a reversible 2H-semiconductor to 1T-metal phase-transition of the surface layer. Electron-phonon coupling of the indirect-bandgap p-doped 2H-MoS2 enables this efficient pathway even at a low density of excited electrons with a distinct optical excitation threshold and saturation behavior. This mechanism needs to be taken into consideration when describing the surface properties of illuminated p-doped 2H-MoS2. In particular, light-induced increased charge mobility and surface activation can cause and enhance the photocatalytic and photoassisted electrochemical hydrogen evolution reaction of water on 2H-MoS2. Generally, it opens up for a way to control not only the surface of p-doped 2H-MoS2 but also related dichalcogenides and layered systems. The findings are based on the sensitivity of time-resolved electron spectroscopy for chemical analysis with photon-energy-tuneable synchrotron radiation.
KW  - catalysis
KW  - dichalcogenides
KW  - hydrogen evolution reaction
KW  - phase transitions
KW  - photoelectron spectroscopy
Y1  - 2021
U6  - https://doi.org/10.1002/adma.202006957
SN  - 0935-9648
SN  - 1521-4095
VL  - 33
IS  - 14
PB  - Wiley-VCH
CY  - Weinheim
ER  -