Binary solvent system used to fabricate fully annealing-free perovskite solar cells

Advanced Energy Materials Wiley 13:11 (2023) 2203468

Authors:

Elena J Cassella, Emma LK Spooner, Joel A Smith, Timothy Thornber, Mary E O'Kane, Robert DJ Oliver, Thomas E Catley, Saqlain Choudhary, Christopher J Wood, Deborah B Hammond, Henry J Snaith, David G Lidzey

Abstract:

High temperature post-deposition annealing of hybrid lead halide perovskite thin films—typically lasting at least 10 min—dramatically limits the maximum roll-to-roll coating speed, which determines solar module manufacturing costs. While several approaches for “annealing-free” perovskite solar cells (PSCs) have been demonstrated, many are of limited feasibility for scalable fabrication. Here, this work has solvent-engineered a high vapor pressure solvent mixture of 2-methoxy ethanol and tetrahydrofuran to deposit highly crystalline perovskite thin-films at room temperature using gas-quenching to remove the volatile solvents. Using this approach, this work demonstrates p-i-n devices with an annealing-free MAPbI3 perovskite layer achieving stabilized power conversion efficiencies (PCEs) of up to 18.0%, compared to 18.4% for devices containing an annealed perovskite layer. This work then explores the deposition of self-assembled molecules as the hole-transporting layer without annealing. This work finally combines the methods to create fully annealing-free devices having stabilized PCEs of up to 17.1%. This represents the state-of-the-art for annealing-free fabrication of PSCs with a process fully compatible with roll-to-roll manufacture.

A Universal Perovskite Nanocrystal Ink for High-Performance Optoelectronic Devices.

Advanced materials (Deerfield Beach, Fla.) 35:8 (2023) e2209486

Authors:

Hochan Song, Jonghee Yang, Woo Hyeon Jeong, Jeongjae Lee, Tack Ho Lee, Jung Won Yoon, Hajin Lee, Alexandra J Ramadan, Robert DJ Oliver, Seong Chan Cho, Seul Gi Lim, Ji Won Jang, Zhongkai Yu, Jae Taek Oh, Eui Dae Jung, Myoung Hoon Song, Sung Heum Park, James R Durrant, Henry J Snaith, Sang Uck Lee, Bo Ram Lee, Hyosung Choi

Abstract:

Semiconducting lead halide perovskite nanocrystals (PNCs) are regarded as promising candidates for next-generation optoelectronic devices due to their solution processability and outstanding optoelectronic properties. While the field of light-emitting diodes (LEDs) and photovoltaics (PVs), two prime examples of optoelectronic devices, has recently seen a multitude of efforts toward high-performance PNC-based devices, realizing both devices with high efficiencies and stabilities through a single PNC processing strategy has remained a challenge.  In this work, diphenylpropylammonium (DPAI) surface ligands, found through a judicious ab-initio-based ligand search, are shown to provide a solution to this problem. The universal PNC ink with DPAI ligands presented here, prepared through a solution-phase ligand-exchange process, simultaneously allows single-step processed LED and PV devices with peak electroluminescence external quantum efficiency of 17.00% and power conversion efficiency of 14.92% (stabilized output 14.00%), respectively. It is revealed that a careful design of the aromatic rings such as in DPAI is the decisive factor in bestowing such high performances, ease of solution processing, and improved phase stability up to 120 days. This work illustrates the power of ligand design in producing PNC ink formulations for high-throughput production of optoelectronic devices; it also paves a path for "dual-mode" devices with both PV and LED functionalities.

Passivation strategies for mitigating defect challenges in halide perovskite light-emitting diodes

Joule Elsevier 7:2 (2023) 272-308

Authors:

Xinyu Shen, Keehoon Kang, Zhongkai Yu, Woo Hyeon Jeong, Hyosung Choi, Sung Heum Park, Samuel D Stranks, Henry J Snaith, Richard H Friend, Bo Ram Lee

Charge transport in mixed metal halide perovskite semiconductors

Nature Materials 22, 216–224 (2023)

Authors:

Satyaprasad P Senanayak*, Krishanu Dey*, Ravichandran Shivanna, Weiwei Li, Dibyajyoti Ghosh, Youcheng Zhang, Bart Roose, Szymon J Zelewski, Zahra Andaji-Garmaroudi, William Wood, Nikhil Tiwale, Judith L MacManus-Driscoll, Richard H Friend, Samuel D Stranks, Henning Sirringhaus

* denotes equal contributing first author.

Abstract:

Investigation of the inherent field-driven charge transport behaviour of three-dimensional lead halide perovskites has largely remained challenging, owing to undesirable ionic migration effects near room temperature and dipolar disorder instabilities prevalent specifically in methylammonium-and-lead-based high-performing three-dimensional perovskite compositions. Here, we address both these challenges and demonstrate that field-effect transistors based on methylammonium-free, mixed metal (Pb/Sn) perovskite compositions do not suffer from ion migration effects as notably as their pure-Pb counterparts and reliably exhibit hysteresis-free p-type transport with a mobility reaching 5.4 cm2 V–1 s−1. The reduced ion migration is visualized through photoluminescence microscopy under bias and is manifested as an activated temperature dependence of the field-effect mobility with a low activation energy (~48 meV) consistent with the presence of the shallow defects present in these materials. An understanding of the long-range electronic charge transport in these inherently doped mixed metal halide perovskites will contribute immensely towards high-performance optoelectronic devices.

Synergistic surface modification of tin-lead perovskite solar cells

Advanced Materials Wiley 35:9 (2023) 2208320

Authors:

Shuaifeng Hu, Pei Zhao, Kyohei Nakano, Robert DJ Oliver, Jorge Pascual, Joel A Smith, Takumi Yamada, Minh Anh Truong, Richard Murdey, Nobutaka Shioya, Takeshi Hasegawa, Masahiro Ehara, Michael B Johnston, Keisuke Tajima, Yoshihiko Kanemitsu, Henry J Snaith, Atsushi Wakamiya

Abstract:

Interfaces in thin-film photovoltaics play a pivotal role in determining device efficiency and longevity. Herein, we study the top surface treatment of mixed tin-lead (∼1.26 eV) halide perovskite films for p-i-n solar cells. We are able to promote charge extraction by treating the perovskite surface with piperazine. This compound reacts with the organic cations at the perovskite surface, modifying the surface structure and tuning the interfacial energy level alignment. In addition, the combined treatment with C<sub>60</sub> pyrrolidine tris-acid (CPTA) reduces hysteresis and leads to efficiencies up to 22.7%, with open-circuit voltage values reaching 0.90 V, ∼92% of the radiative limit for the band gap of this material. The modified cells also show superior stability, with unencapsulated cells retaining 96% of their initial efficiency after >2000 hours of storage in N<sub>2</sub> and encapsulated cells retaining 90% efficiency after >450 hours of storage in air. Intriguingly, CPTA preferentially binds to Sn<sup>2+</sup> sites at film surface over Pb<sup>2+</sup> due to the energetically favoured exposure of the former, according to first-principles calculations. This work provides new insights into the surface chemistry of perovskite films in terms of their structural, electronic, and defect characteristics and we use this knowledge to fabricate state-of-the-art solar cells.