A 2D/3D Heterostructure Perovskite Solar Cell with a Phase‐Pure and Pristine 2D Layer

M Meng‐Chen Shih (Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA) S Shaun Tan (Department of Chemistry) Y Yongli Lu (Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA) T Tim Kodalle (Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Rd., Berkeley, California 94720, United States) D Do‐Kyoung Lee (Molecular Foundry Lawrence Berkeley National Laboratory Berkeley CA 94720 USA) Y Yifan Dong (Frontier Institute of Science and Technology) B Bryon W. Larson (Chemistry and Nanoscience Center National Renewable Energy Laboratory (NREL) 15013 Denver West Parkway Golden CO 80401 USA) S Soyeon Park R Ruiqi Zhang M Matthias J. Grotevent (Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States) T Tara Sverko (Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA) H Hua Zhu Y Yu‐Kuan Lin (Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA) C Carolin M. Sutter‐Fella (Molecular Foundry Division Lawrence Berkeley National Laboratory 67 Cyclotron Road Berkeley CA 94720 USA) K Kai Zhu M Matthew C. Beard (National Renewable Energy Laboratory) V Vladimir Bulović M Moungi G. Bawendi (Department of Chemistry)

Abstract

AbstractInterface engineering plays a critical role in advancing the performance of perovskite solar cells. As such, 2D/3D perovskite heterostructures are of particular interest due to their optoelectrical properties and their further potential improvements. However, for conventional solution‐processed 2D perovskites grown on an underlying 3D perovskite, the reaction stoichiometry is normally unbalanced with excess precursors. Moreover, the formed 2D perovskite is impure, leading to unfavorable energy band alignment at the interface. Here a simple method is presented that solves both issues simultaneously. The 2D formation reaction is taken first to completion, fully consuming excess PbI2. Then, isopropanol is utilized to remove excess organic ligands, control the 2D perovskite thickness, and obtain a phase‐pure, n = 2, 2D perovskite. The outcome is a pristine (without residual 2D precursors) and phase‐pure 2D perovskite heterostructure with improved surface passivation and charge carrier extraction compared to the conventional solution process. PSCs incorporating this treatment demonstrate a notable improvement in both stability and power conversion efficiency, with negligible hysteresis, compared to the conventional process.

Article Details

Volume / Issue Vol. 37, Issue 17
Published April 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (18)

M

Meng‐Chen Shih

Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA

S

Shaun Tan

Department of Chemistry

Y

Yongli Lu

Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA

T

Tim Kodalle

Molecular Foundry, Lawrence Berkeley National Laboratory, 1 Cyclotron Rd., Berkeley, California 94720, United States

D

Do‐Kyoung Lee

Molecular Foundry Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

Y

Yifan Dong

Frontier Institute of Science and Technology

B

Bryon W. Larson

Chemistry and Nanoscience Center National Renewable Energy Laboratory (NREL) 15013 Denver West Parkway Golden CO 80401 USA

S

Soyeon Park

R

Ruiqi Zhang

M

Matthias J. Grotevent

Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States

T

Tara Sverko

Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA

H

Hua Zhu

Y

Yu‐Kuan Lin

Department of Chemistry Massachusetts Institute of Technology 77 Massachusetts Avenue Cambridge MA 02139 USA

C

Carolin M. Sutter‐Fella

Molecular Foundry Division Lawrence Berkeley National Laboratory 67 Cyclotron Road Berkeley CA 94720 USA

K

Kai Zhu

M

Matthew C. Beard

National Renewable Energy Laboratory

V

Vladimir Bulović

M

Moungi G. Bawendi

Department of Chemistry