Surface engineering gets the red light

Surface engineering gets the red light
Passivating the surface of perovskite nanocrystals with IDA molecules improves their stability and their optical and electrical properties, making them useful for optoelectronic devices. Credit: KAUST

Perovskite particles could improve the performance of solar cells and light-emitting diodes via a simple process to stabilize the nanocrystal surface.

A method for chemically stabilizing optical nanocrystals, without degrading their electrical properties, has been developed by scientists at KAUST.

Halide perovskites are in an exciting class of materials for optoelectronics and photovoltaics. These materials efficiently absorb visible light, possess long charge-carrier diffusion lengths and are easy and cheap to produce. The performance of optical devices can also be improved by incorporating nanometer-scale particles, which have far superior light-emitting and -absorbing properties than the bulk material from which they are derived. So it is unsurprising that scientists are keen to combine these two approaches. The challenge is that tiny perovskite particles aren't always chemically stable, and their atomic crystal structure is difficult to control.

Attaching molecules, referred to as ligands, can stabilize a nanocrystal. But this so-called passivation can form an electrically insulating shell around the particle that inhibits their effectiveness in electronic devices.

Now, Osman Bakr's group, and co-workers from KAUST and ShanghaiTech University, has created halide perovskite nanocrystals made from cesium-lead-iodide passivated by 2,2′-iminodibenzoic acid (IDA) ligands. They show that this provides the necessary chemical stability while remaining useful for optoelectronics. And the passivation was simple: just adding IDA powder into the nanocrystal solution and using a centrifuge to remove any excess.

The team chose IDA because it is a bidentate ligand, meaning that it bonds to the nanocrystal at two sites. "The conventional ligands used in these applications, such as oleic acid, are dynamic on the surface of the perovskite nanocrystals and easily come loose," says Jun Pan, the first author on the paper. "That's why we apply a double carboxylic group to strongly bind on the surface, which also stabilizes the perovskite crystal phase at room temperature."

Pan and his team compared the optical properties of both the passivated and unpassivated samples and observed that the treatment improved the photoluminescent quantum yield—a measure of how many photons are emitted for every photon absorbed—from 80 percent to over 95 percent. And while the intensity of light emitted from the unpassivated nanocrystals had dropped significantly five days later, the IDA-treated samples were still emitting light at 90 percent of their initial level 15 days later.

The team demonstrated that their stabilized halide perovskite nanocrystals were suitable for optoelectronic applications by using them to build . The red-light generating devices again outperformed the unpassivated control device in terms of maximum luminance and luminous power efficiency.

"The next step is to realize more stable perovskite structures and to create an LED with performance above 10 percent based on ," says Pan.


Explore further

Novel capping strategy improves stability of perovskite nanocrystals

More information: Jun Pan et al. Bidentate Ligand-Passivated CsPbI3 Perovskite Nanocrystals for Stable Near-Unity Photoluminescence Quantum Yield and Efficient Red Light-Emitting Diodes, Journal of the American Chemical Society (2017). DOI: 10.1021/jacs.7b10647
Citation: Surface engineering gets the red light (2018, April 25) retrieved 19 May 2019 from https://phys.org/news/2018-04-surface-red.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
5 shares

Feedback to editors

User comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more