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None, Akriti

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Anion diffusion in two-dimensional halide perovskites

Commercialization of halide perovskites in the semiconductor industry is hindered by their short-term stability. The instability of perovskites is closely interlinked with ionic diffusion. Historically, attempts to study diffusion in 2D perovskites mostly utilized electrical characterizations, but these characterizations pose a challenge in deconvoluting the impact of device architecture, interlayers, and ionic species. In this Perspective, we focus our attention on simple optical characterizations employed in the literature to investigate halide diffusion in 2D perovskites using lateral and vertical heterostructure platforms. We review the various synthesis techniques used for fabrication of halide perovskite heterostructures and discuss the qualitative and quantitative diffusion studies performed using these platforms. We discuss the numerical methods used to validate and supplement the experimental halide diffusion kinetics. Finally, we highlight the need to conduct further research on the impact of device operating conditions, lattice structure, and vacancy concentration on halide diffusion. Through this Perspective, we aim to emphasize the need of developing a comprehensive understanding of halide diffusion in perovskites for their successful deployment in optoelectronics.

36 MATERIALS SCIENCE↗

Quantifying Anionic Diffusion in 2D Halide Perovskite Lateral Heterostructures

Anionic diffusion strongly impacts the stability of halide perovskite materials, but it is still not well understood. Here, a quantitative investigation of in-plane thermally driven anionic inter-diffusion in a series of novel 2D and quasi-2D halide perovskites lateral heterostructures is reported. The calculated diffusion coefficients (D) reveal the inhibition of Br–I inter-diffusion with bulky π-conjugated organic cations compared with short-chain aliphatic organic cations. Furthermore, halide diffusion is found to be faster in quasi-2D (n > 1) than 2D perovskites (n = 1). The increment becomes less apparent as the “n” number increases, akin to the quantum confinement effect observed for band gaps. These trends are rationalized by molecular dynamics simulations of free energy barriers for halide diffusion that reveal mechanisms for suppressing diffusion. We report this work provides important fundamental insights on the anionic migration and diffusion process in halide perovskite materials.

2D materials↗