Interfacial Engineering of Nickel Oxide-Perovskite Interface with Amino Acid Complexed NiO to Improve Perovskite Solar Cell Performance.

The interface between NiO and perovskite in inverted perovskite solar cells (PSCs) is a major factor that can limit device performance due to defects and inappropriate redox reactions, which cause nonradiative recombination and decrease in open-circuit voltage (VOC). In the present study, a novel approach is used for the first time, where an amino acid (glycine (Gly), alanine (Ala), and aminobutyric acid (ABA))-complexed NiO are used as interface modifiers to eliminate defect sites and hydroxyl groups from the surface of NiO. The Ala-complexed NiO suppresses interfacial non-radiative recombination, improves the perovskite layer quality and better energy band alignment with the perovskite, resulting in improved charge transfer and reduced recombination.

Suppressing Redox Reactions at the Perovskite-Nickel Oxide Interface with Zinc Nitride to Improve the Performance of Perovskite Solar Cells.

For p-i-n perovskite solar cells (PSCs), nickel oxide (NiO) hole transport layers (HTLs) are the preferred interfacial layer due to their low cost, high mobility, high transmittance, and stability. However, the redox reaction between the Ni and hydroxyl groups in the NiO and perovskite layer leads to oxidized CHNH and reacts with PbI in the perovskite, resulting in a large number of non-radiative recombination sites. Among various transition metals, an ultra-thin zinc nitride (ZnN) layer on the NiO surface is chosen to prevent these redox reactions and interfacial issues using a simple solution process at low temperatures.

Chemical Bridge-Mediated Heterojunction Electron Transport Layers Enable Efficient and Stable Perovskite Solar Cells.

Perovskite solar cells (PSCs) emerged as potential photovoltaic energy-generating devices developing in recent years because of their excellent photovoltaic properties and ease of processing. However, PSCs are still reporting efficiencies much lower than their theoretical limits owing to various losses caused by the charge transport layer and the perovskite. In this regard, herein, an interface engineering strategy using functional molecules and chemical bridges was applied to reduce the loss of the heterojunction electron transport layer.

Enhanced Device Performances of MAFACsPb(IBr) Perovskite Solar Cells with Dual-Functional 2-Chloroethyl Acrylate Additives.

Perovskite photovoltaics (PePVs) tend to suffer from a high density of defects that restrict the device in terms of performances and stability. Therefore, defect passivation and film-quality improvement of perovskite active layers are crucial for high-performance PePVs. In this work, 2-chloroethyl acrylate (CEA) with C═O and -Cl groups in CsFAMAPb (IBr) precursor solutions is introduced as a novel bifunctional additive to act as both a defect passivator and perovskite-growth controller.

Non-Fullerene Small Molecule Electron-Transporting Materials for Efficient p-i-n Perovskite Solar Cells.

PCBM is commonly used in perovskite solar cells (PSC) as the electron transport material (ETM). However, PCBM film has various disadvantages, such as its low coverage or the many pinholes that appear due to its aggregation behavior. These faults may lead to undesirable direct contact between the metal cathode and perovskite film, which could result in charge recombination at the perovskite/metal interface.