Researchers at Oxford University and Exciton Science have demonstrated a new way to create stable perovskite solar cells, with fewer defects and the potential to finally rival silicon's durability.

By removing the solvent dimethyl-sulfoxide and introducing dimethylammonium chloride as a crystallisation agent, the researchers were able to better control the intermediate phases of the perovskite crystallisation process, leading to thin films of greater quality, with reduced defects and enhanced stability.

Large groups of up to 138 sample devices were then subjected to a rigorous accelerated ageing and testing process at high temperatures and in real-world conditions.

Formamidinium-caesium perovskite solar cells created using the new synthesis process significantly outperformed the control group and demonstrated resistance to thermal, humidity and light degradation.

This is a strong step forward to matching commercial silicon's stability and makes perovskite-silicon tandem devices a much more realistic candidate for becoming the dominant next-generation solar cell.

Led by Professor Henry Snaith (Oxford University) and Professor Udo Bach (Monash University), the work has been published in the journal Nature Materials and is available here.

Oxford University PhD student Philippe Holzhey, a Marie Curie Early Stage Researcher and joint first author on the work, said: "It's really important that people start shifting to realise there is no value in performance if it's not a stable performance.

"If the device lasts for a day or a week or something, there's not so much value in it. It has to last for years."

During testing, the best device operated above the T80 threshold for over 1,400 hours under simulated sunlight at 65 C. T80 is the time it takes for a solar cell to reduce to 80% of its initial efficiency, a common benchmark within the research field.

Beyond 1,600 hours, the control device fabricated using the conventional dimethyl-sulfoxide approach stopped functioning, while devices fabricated with the new, improved design retained 70% of their original efficiency, under accelerated aging conditions.

The same degradation study was performed on a group of devices at the very high temperature of 85 C, with the new cells again outperforming the control group.

Extrapolating from the data, the researchers calculated that the new cells age by a factor of 1.7 for each 10 C increase in the temperature they are exposed to, which is close to the 2-fold increase expected of commercial silicon devices.

Dr David McMeekin, the corresponding and joint first author on the paper, was an Australian Centre for Advanced Photovoltaics (ACAP) Postdoctoral Fellow at Monash University and is now a Marie Sklodowska-Curie Postdoctoral Fellow at Oxford University.

He said: "I think what separates us from other studies is that we've done a lot of accelerated aging. We've aged the cells at 65 C and 85 C under the whole light spectrum."

The number of devices used in the study is also significant, with many other perovskite research projects limited to just one or two prototypes.

"Most studies only show one curve without any standard deviation or any kind of statistical approach to determine if this design is more stable than the other," David added.

The researchers hope their work will encourage a greater focus on the intermediate phase of perovskite crystallisation as an important factor in achieving greater stability and commercial viability.

This work was supported by the Stanford Linear Accelerator Center (SLAC) and the National Renewable Energy Laboratory (NREL).

Perovskites
Artificially synthesised in laboratory conditions, semiconductor thin films made up of perovskite compounds are far cheaper to make than silicon solar cells, with greater flexibility and a tunable band gap.

They emerged unexpectedly in the last decade and have reached impressive power-conversion efficiencies of over 25%.

However, too much focus has been placed on creating the most efficient perovskite solar cell, rather than resolving the fundamental problems inhibiting the material from being used in widespread commercial applications.

Compared to silicon, perovskites can degrade rapidly in real world conditions, with exposure to heat and moisture causing damage and negatively impacting device performance.

Solving these stability issues is the key challenge for perovskites in their quest to take on, or "boost" silicon via a tandem architecture and take their place in the commercial photovoltaics landscape.

Research Report:Intermediate-phase engineering via dimethylammonium cation additive for stable perovskite solar cells

Related Links
ARC Centre of Excellence in Exciton Science
All About Solar Energy at SolarDaily.com

Tweet

Thanks for being here; We need your help. The SpaceDaily news network continues to grow but revenues have never been harder to maintain. With the rise of Ad Blockers, and Facebook - our traditional revenue sources via quality network advertising continues to decline. And unlike so many other news sites, we don't have a paywall - with those annoying usernames and passwords. Our news coverage takes time and effort to publish 365 days a year. If you find our news sites informative and useful then please consider becoming a regular supporter or for now make a one off contribution.
SpaceDaily Contributor $5 Billed Once credit card or paypal		SpaceDaily Monthly Supporter $5 Billed Monthly paypal only

Sierra Space selected by Maxar to provide solar power solutions for constellation of proliferated LEO satellites
Louisville CO (SPX) Dec 06, 2022
Sierra Space, a leading space company building an end-to-end business and technology platform in space to benefit life on Earth, reports that the company won a significant space defense contract with Maxar. Under the agreement, Sierra Space will provide revolutionary solar power solutions and production capability. This contract will support a constellation of 14 satellites that use Maxar's proliferated low Earth orbit (LEO) spacecraft platform, which are designed to support a wide variety of glob ... read more