Improved Hole Extraction and Band Alignment via Interface Modification in Hole Transport Material‐Free Ag/Bi Double Perovskite Solar Cells

Author:

Schmitz Fabian1ORCID,Bhatia Ribhu2,Burkhart Julian1,Schweitzer Pascal13,Allione Marco4,Gallego Jaime1,Piotrowski Piotr5,Cajzl Jakub5,Paszke Piotr5,Mohan Das Gour5,Pawlak Dorota A.5,Bella Federico4,Schlettwein Derck13,Lamberti Francesco67,Meloni Simone2,Gatti Teresa14ORCID

Affiliation:

1. Center for Materials Research Justus Liebig University Heinrich‐Buff‐Ring 17 35392 Giessen Germany

2. Department of Chemical and Pharmaceutical Sciences Università of Ferrara Via Luigi Borsari 46 I‐44121 Ferrara Italy

3. Institute of Applied Physics Justus Liebig University Heinrich‐Buff‐Ring 16 35392 Giessen Germany

4. Department of Applied Science and Technology Politecnico di Torino C.so Duca degli Abruzzi 24 10129 Torino Italy

5. Centre of Excellence ENSEMBLE3 sp. z o. o. Wólczyńska 133 01‐919 Warsaw Poland

6. Department of Chemical Sciences University of Padova Via Marzolo 1 35131 Padova Italy

7. Department of Information Engineering University of Padova Via Gradenigo 6a 35131 Padova Italy

Abstract

Within one decade, lead halide perovskite solar cells have reached power conversion efficiencies (PCEs) compatible with that of silicon solar cells. While in the beginning, they suffered from short device lifetimes, those have also been strongly improved over time. However, their content of toxic lead still poses a risk of environmental pollution and human health on exposure. The double perovskite (DP) Cs2AgBiBr6 offers the potential to be a lead‐free alternative light‐harvesting material. Herein, the fabrication of hole transport material (HTM)‐free Cs2AgBiBr6‐based solar cells is presented, in which the DP surface is modified via a n‐butylammonium posttreatment to create a 2D/3D mixed interface. Additionally, the commonly utilized metal electrode and HTM are substituted with a carbon black back electrode (CBE) consisting of up‐cycled biowaste. Through the 2D/3D interface modification, charge recombination is suppressed, and band alignment is improved at the perovskite/CBE interface. Additionally, density functional theory calculations reveal that an increasing 2D modification thickness enhances the probability for holes in Cs2AgBiBr6 to be located close to the perovskite/CBE interface, further supporting their extraction. Overall, the PCE of the HTM‐free solar cells is improved through the implementation of a low‐cost and end‐of‐waste fabrication strategy.

Funder

HORIZON EUROPE European Research Council

Publisher

Wiley

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