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.

Reducing Nonradiative Losses in Perovskite LEDs Through Atomic Layer Deposition of Al2O3 on the Hole-injection Contact

University of Oxford (2023)

Authors:

Emil Dyrvik, Robert Taylor, Alexandra Ramadan, Jonathan Warby, Andreas Lauritzen, Karl-Augustin Zaininger, Henry Snaith, Suhas Mahesh, Melissa McCarthy

Abstract:

Experimental research data collected in laboratories at the Clarendon Laboratory, 2020-2022.

Device Performance of Emerging Photovoltaic Materials (Version 3)

Advanced Energy Materials Wiley 13:1 (2023)

Authors:

Osbel Almora, Derya Baran, Guillermo C Bazan, Carlos I Cabrera, Sule Erten‐Ela, Karen Forberich, Fei Guo, Jens Hauch, Anita WY Ho‐Baillie, T Jesper Jacobsson, Rene AJ Janssen, Thomas Kirchartz, Nikos Kopidakis, Maria A Loi, Richard R Lunt, Xavier Mathew, Michael D McGehee, Jie Min, David B Mitzi, Mohammad K Nazeeruddin, Jenny Nelson, Ana F Nogueira, Ulrich W Paetzold, Barry P Rand, Uwe Rau, Henry J Snaith, Eva Unger, Lídice Vaillant‐Roca, Chenchen Yang, Hin‐Lap Yip, Christoph J Brabec

Regulating surface potential maximizes voltage in all-perovskite tandems.

Nature 613:7945 (2023) 676-681

Authors:

Hao Chen, Aidan Maxwell, Chongwen Li, Sam Teale, Bin Chen, Tong Zhu, Esma Ugur, George Harrison, Luke Grater, Junke Wang, Zaiwei Wang, Lewei Zeng, So Min Park, Lei Chen, Peter Serles, Rasha Abbas Awni, Biwas Subedi, Xiaopeng Zheng, Chuanxiao Xiao, Nikolas J Podraza, Tobin Filleter, Cheng Liu, Yi Yang, Joseph M Luther, Stefaan De Wolf, Mercouri G Kanatzidis, Yanfa Yan, Edward H Sargent

Abstract:

The open-circuit voltage (VOC) deficit in perovskite solar cells is greater in wide-bandgap (over 1.7 eV) cells than in perovskites of roughly 1.5 eV (refs. 1,2). Quasi-Fermi-level-splitting measurements show VOC-limiting recombination at the electron-transport-layer contact3-5. This, we find, stems from inhomogeneous surface potential and poor perovskite-electron transport layer energetic alignment. Common monoammonium surface treatments fail to address this; as an alternative, we introduce diammonium molecules to modify perovskite surface states and achieve a more uniform spatial distribution of surface potential. Using 1,3-propane diammonium, quasi-Fermi-level splitting increases by 90 meV, enabling 1.79 eV perovskite solar cells with a certified 1.33 V VOC and over 19% power conversion efficiency (PCE). Incorporating this layer into a monolithic all-perovskite tandem, we report a record VOC of 2.19 V (89% of the detailed balance VOC limit) and over 27% PCE (26.3% certified quasi-steady state). These tandems retained more than 86% of their initial PCE after 500 h of operation.