MoS2 nanocage anodes synthesized by a bubble-template-assisted method can provide a large expandable area to stabilize the electrode structure during cycling.
Because the surface-to-volume ratio of quasi-two-dimensional materials is extremely high, understanding their surface characteristics is crucial for practically controlling their intrinsic properties and fabricating p-type and n-type layered semiconductors. Van der Waals crystals are expected to have an inert surface because of the absence of dangling bonds. However, here we show that the surface of high-quality synthesized molybdenum disulfide (MoS2) is a major n-doping source. The surface electron concentration of MoS2 is nearly four orders of magnitude higher than that of its inner bulk. Substantial thickness-dependent conductivity in MoS2 nanoflakes was observed. The transfer length method suggested the current transport in MoS2 following a two-dimensional behavior rather than the conventional three-dimensional mode. Scanning tunneling microscopy and angle-resolved photoemission spectroscopy measurements confirmed the presence of surface electron accumulation in this layered material. Notably, the in situ-cleaved surface exhibited a nearly intrinsic state without electron accumulation.
Two-dimensional Dion–Jacobson
(DJ) perovskites have shown
improved structure stability in comparison with Ruddlesden–Popper
(RP) perovskites. However, the mechanism behind the improved stability
is still largely unexplored. Here a multifluorinated aromatic spacer,
namely, 4F-PhDMA, has been successfully developed for 2D DJ perovskites.
It is found that the 2D DJ perovskite with a 4F-PhDMA spacer exhibits
a high dissociation energy due to the multiple noncovalent interactions.
The optimized 2D DJ device based on the 4F-PhDMA spacer (n = 4) exhibits a champion efficiency of 16.62% with much improved
light and thermal stability. This efficiency is much higher than that
of the control device using an unfluorinated spacer (n = 4, PCE = 10.11%) and is among the highest efficiencies in aromatic-spacer-based
2D DJ perovskite solar cells (PSCs). Our work highlights the importance
of incorporating multiple noncovalent interactions in the 2D DJ perovskite
by employing a multifluorinated aromatic spacer to achieve DJ PSCs
with both high efficiency and high stability.
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