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Structural and chemical evolution of methylammonium lead halide perovskites during thermal processing from solution

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In this paper, the evolution of perovskites formed from targeted precursor chemistries was investigated by correlating in situ temperature-dependent X-ray diffraction, thermogravimetric analysis, and mass spectral analysis of the evolved species.
Abstract
Following the prominent success of CH3NH3PbI3 in photovoltaics and other optoelectronic applications, focus has been placed on better understanding perovskite crystallization from precursor and intermediate phases in order to facilitate improved crystallinity often desirable for advancing optoelectronic properties. Understanding of stability and degradation is also of critical importance as these materials seek commercial applications. In this study, we investigate the evolution of perovskites formed from targeted precursor chemistries by correlating in situ temperature-dependent X-ray diffraction, thermogravimetric analysis, and mass spectral analysis of the evolved species. This suite of analyses reveals important precursor composition-induced variations in the processes underpinning perovskite formation and degradation. The addition of Cl− leads to widely different precursor evolution and perovskite formation kinetics, and results in significant changes to the degradation mechanism, including suppression of crystalline PbI2 formation and modification of the thermal stability of the perovskite phase. This work highlights the role of perovskite precursor chemistry in both its formation and degradation.

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Journal ArticleDOI

Band-Aligned Polymeric Hole Transport Materials for Extremely Low Energy Loss α-CsPbI3 Perovskite Nanocrystal Solar Cells

TL;DR: In this article, a CsPbI3 perovskite quantum dot (QD) solar cells with a remarkable efficiency approaching 13% and an extremely low energy loss of 0.45 eV by employing a series of dopant-free polymeric hole-transporting materials (HTMs).
Journal ArticleDOI

Highly Air-Stable Carbon-Based α-CsPbI3 Perovskite Solar Cells with a Broadened Optical Spectrum

TL;DR: In this paper, an α-Cesium lead halide perovskite (C-CsPbI3) was obtained in dry air (temperature: 20-30 °C; humidity: 10-20%).
Journal ArticleDOI

Metal Halide Perovskites in Quantum Dot Solar Cells: Progress and Prospects

TL;DR: In this article, the development of nanoscale metal halide perovskite semiconductors has gained prominence surpassing all other QD materials in terms of efficiency, and are becoming a platform for further improving technology to solve big energy challenges.
References
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Journal ArticleDOI

Organometal Halide Perovskites as Visible-Light Sensitizers for Photovoltaic Cells

TL;DR: Two organolead halide perovskite nanocrystals were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells, which exhibit strong band-gap absorptions as semiconductors.
Journal ArticleDOI

Efficient Hybrid Solar Cells Based on Meso-Superstructured Organometal Halide Perovskites

TL;DR: A low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight is reported.
Journal ArticleDOI

Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

TL;DR: In this article, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
Journal Article

Electron-Hole Diffusion Lengths Exceeding 1 Micrometer in an Organometal Trihalide Perovskite Absorber

TL;DR: In this paper, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
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This work highlights the role of perovskite precursor chemistry in both its formation and degradation.