Muriel Bouttemy | Searcharxiv

arXiv2025

Collective Fluorescence of Graphene Quantum Dots on a surface

This study explores the organization of graphene quantum dots on the surface of monocrystalline halide perovskite. We show that graphene quantum dots tends to aggregate on the surface of perovskite unlike in solution or on other substrates, even at very low concentration of the initial solution that should yield single-molecule samples. Spectral analysis on small clusters shows a back-and-forth dynamical transition between an uncoupled, monomer-like state, and an excimer state. Following this "dance" between states, a drastic one-way increase in fluorescence intensity combined with a shortening of the excited state lifetime has been observed on some clusters. This behavior is related to the emission of a collective state that may be a consequence of the dynamical organization of graphene quantum dots under illumination on the surface of the perovksite.

cond-mat.mes-hall↗

arXiv2019

Strong Performance Enhancement in Lead-Halide Perovskite Solar Cells through Rapid, Atmospheric Deposition of n-type Buffer Layer Oxides

Thin (approximately 10 nm) oxide buffer layers grown over lead-halide perovskite device stacks are critical for protecting the perovskite against mechanical and environmental damage. However, the limited perovskite stability restricts the processing methods and temperatures (<=110 C) that can be used to deposit the oxide overlayers, with the latter limiting the electronic properties of the oxides achievable. In this work, we demonstrate an alternative to existing methods that can grow pinhole-free TiOx (x = 2.00+/-0.05) films with the requisite thickness in <1 min without vacuum. This technique is atmospheric pressure chemical vapor deposition (AP-CVD). The rapid but soft deposition enables growth temperatures of >=180 °C to be used to coat the perovskite. This is >=70 °C higher than achievable by current methods and results in more conductive TiOx films, boosting solar cell efficiencies by >2%. Likewise, when AP-CVD SnOx (x ~ 2) is grown on perovskites, there is also minimal damage to the perovskite beneath. The SnOx layer is pinhole-free and conformal, which reduces shunting in devices, and increases steady-state efficiencies from 16.5% (no SnOx) to 19.4% (60 nm SnOx), with fill factors reaching 84%. This work shows AP-CVD to be a versatile technique for growing oxides on thermally-sensitive materials.

physics.app-ph↗