MRS Meetings and Events

 

EN02.08.22 2022 MRS Fall Meeting

Cathode Interlayer Engineering with Vacuum Thermal Evaporated N-type Rylene Diimide Derivatives in Highly Efficient Inverted Perovskite Solar Cells

When and Where

Nov 30, 2022
8:00pm - 10:00pm

Hynes, Level 1, Hall A

Presenter

Co-Author(s)

Hye Seung Kim1,Myoung Hoon Song1

Ulsan National Institute of Science and Technology1

Abstract

Hye Seung Kim1,Myoung Hoon Song1

Ulsan National Institute of Science and Technology1
In inverted perovskite solar cells (PeSCs), choosing cathode interlayer plays key role in determining performance of solar cell. Among various processing methods, vacuum thermal evaporation (VTE) is already adopted in electron transporting layer (ETL) such as C<sub>60</sub> and cathode interlayer such as bathocuproine (BCP), LiF and Ca in inverted PeSCs. Especially, cathode interlayer have been already utilized to suppress the interfacial resistance and lower the energy barrier between ETL and cathode. N-type rylene diimide derivatives such as perylene diimide (PDI) and naphtahlene diimide (NDI) have attracted great attention due to their advantages of easy molecular modification, high electron mobility and good thermal and chemical stability so that have been applied to cathode interlayer by solution processing such as spin-coating method.<br/>In this study, we demonstrate for the first time rylene diimide derivatives such as PDI and NDI family organic small molecules as cathode interlayer candidates using VTE method. Rylene diimide derivatives films show thin thickness about ~5 nm. In comparison with widely used BCP, underlying rylene diimide materials exhibit different silver cathode growth phenomenon. In addition, we compare the effect as a cathode interlayer by considering the energy levels and metal cathode growth phenomenon by the number of amine-functionalized groups of each material.<br/>Consequently, the PeSC with N,N'-Bis[3-(dimethylamino)propyl]perylene-3,4,9,10-tetracarboxylic diimide (PDIN) shows a enhanced power conversion efficiency (PCE) of 21.60%, which is higher than that of the PeSC without cathode interlayer and with BCP or NDI-based interlayer. Excluding the solvent consideration in solution processing, PDI-based materials that are easily vacuum thermal evaporated are expected to be in the spotlight in inverted PeSCs for cathode interlayer.

Keywords

physical vapor deposition (PVD)

Symposium Organizers

Jin-Wook Lee, Sungkyunkwan University
Carolin Sutter-Fella, Lawrence Berkeley National Laboratory
Wolfgang Tress, Zurich University of Applied Sciences
Kai Zhu, National Renewable Energy Laboratory

Symposium Support

Bronze
ACS Energy Letters
ChemComm
MilliporeSigma
SKKU Insitute of Energy Science & Technology

Session Chairs

Jin-Wook Lee
Carolin Sutter-Fella
Wolfgang Tress

In this Session

EN02.08.01
Utilisation of PEDOT as a Hole Selective Layer for Reproducible Efficient Tin-Based Perovskite Solar Cells with the DMSO-Free Solvent System

EN02.08.02
Tuning the Surface Potential of Hybrid Perovskite Active Layers Through Interfacial Engineering Using Fluorinated Compounds

EN02.08.03
Hole-Transporting Self-Assembled Monolayer Enables 23.1%-Efficient Single-Crystal Perovskite Solar Cells with Enhanced Stability

EN02.08.04
Solvent Engineering of NiOx Solutions for Rapid Depositions as Hole Transporting Layers for Flexible Perovskite Solar Cells

EN02.08.05
Potentiometry of Operating Perovskite-Based Devices with Kelvin Probe Force Microscopy

EN02.08.06
Low Temperature Synthesized Y:SnO2 as an Effective Electron Transport Layer for Inverted Perovskite Solar Cells on Flexible ITO-PET Substrate

EN02.08.08
Enabling Perovskite/Perovskite/Silicon Triple Tandem Based on Transparent Conductive Adhesive Lamination Process

EN02.08.09
Defect-Stabilized Tin-Based Perovskite Solar Cells Enabled by Multi-Functional Molecular Additives

EN02.08.10
Perovskite-Based Multijunction Solar Cells for Efficient Continuous Solar-Assisted Water Splitting

EN02.08.11
In Situ Metrology of Hybrid Halide Perovskite Single Crystals—Investigating Growth Dynamics of Inverse Temperature Crystallisation

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