Engineering ligand reactivity enables high-temperature operation of stable perovskite solar cells

Author:

Park So Min1ORCID,Wei Mingyang2ORCID,Xu Jian1,Atapattu Harindi R.3ORCID,Eickemeyer Felix T.2ORCID,Darabi Kasra4,Grater Luke1ORCID,Yang Yi5ORCID,Liu Cheng5ORCID,Teale Sam1ORCID,Chen Bin15ORCID,Chen Hao1ORCID,Wang Tonghui4ORCID,Zeng Lewei1,Maxwell Aidan1ORCID,Wang Zaiwei1ORCID,Rao Keerthan R.3ORCID,Cai Zhuoyun6,Zakeeruddin Shaik M.2ORCID,Pham Jonathan T.6ORCID,Risko Chad M.3ORCID,Amassian Aram4ORCID,Kanatzidis Mercouri G.5ORCID,Graham Kenneth R.3ORCID,Grätzel Michael2ORCID,Sargent Edward H.157ORCID

Affiliation:

1. Department of Electrical and Computer Engineering, University of Toronto, 10 King’s College Road, Toronto, Ontario M5S 3G4, Canada.

2. Laboratory of Photonics and Interfaces, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland.

3. Department of Chemistry, University of Kentucky, Lexington, KY 40506, USA.

4. Department of Materials Science and Engineering, and Organic and Carbon Electronics Laboratories (ORaCEL), North Carolina State University, Raleigh, NC 27695, USA.

5. Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.

6. Department of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA.

7. Department of Electrical and Computer Engineering, Northwestern University, Evanston, IL 60208, USA.

Abstract

Perovskite solar cells (PSCs) consisting of interfacial two- and three-dimensional heterostructures that incorporate ammonium ligand intercalation have enabled rapid progress toward the goal of uniting performance with stability. However, as the field continues to seek ever-higher durability, additional tools that avoid progressive ligand intercalation are needed to minimize degradation at high temperatures. We used ammonium ligands that are nonreactive with the bulk of perovskites and investigated a library that varies ligand molecular structure systematically. We found that fluorinated aniliniums offer interfacial passivation and simultaneously minimize reactivity with perovskites. Using this approach, we report a certified quasi–steady-state power-conversion efficiency of 24.09% for inverted-structure PSCs. In an encapsulated device operating at 85°C and 50% relative humidity, we document a 1560-hour T 85 at maximum power point under 1-sun illumination.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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