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.

Naphthalene-imide Self-assembled Monolayers as a Surface Modification of ITO for Improved Thermal Stability of Perovskite Solar Cells

ACS Applied Energy Materials American Chemical Society (ACS) 6:2 (2023) 667-677

Authors:

Sebastian O Fürer, Kevin J Rietwyk, Federico Pulvirenti, David P McMeekin, Maciej Adam Surmiak, Sonia R Raga, Wenxin Mao, Xiongfeng Lin, Yvonne Hora, Jian Wang, Yangwei Shi, Stephen Barlow, David S Ginger, Seth R Marder, Udo Bach

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.

Efficient and stable formamidinium–caesium perovskite solar cells and modules from lead acetate-based precursors

Energy & Environmental Science Royal Society of Chemistry (RSC) 16:1 (2023) 138-147

Authors:

Jie Zhao, Sebastian O Fürer, David P McMeekin, Qingdong Lin, Pin Lv, Jisheng Ma, Wen Liang Tan, Chao Wang, Boer Tan, Anthony SR Chesman, Huiyu Yin, Andrew D Scully, Christopher R McNeill, Wenxin Mao, Jianfeng Lu, Yi-Bing Cheng, Udo Bach

Organic solvent free PbI2 recycling from perovskite solar cells using hot water.

Journal of hazardous materials Elsevier 447 (2023) 130829

Authors:

Felix Schmidt, Meret Amrein, Sebastian Hedwig, Manuel Kober-Czerny, Adriana Paracchino, Ville Holappa, Riikka Suhonen, Andreas Schäffer, Edwin C Constable, Henry J Snaith, Markus Lenz

Abstract:

Perovskite solar cells represent an emerging and highly promising renewable energy technology. However, the most efficient perovskite solar cells critically depend on the use of lead. This represents a possible environmental concern potentially limiting the technologies' commercialization. Here, we demonstrate a facile recycling process for PbI<sub>2</sub>, the most common lead-based precursor in perovskite absorber material. The process uses only hot water to effectively extract lead from synthetic precursor mixes, plastic- and glass-based perovskites (92.6 - 100% efficiency after two extractions). When the hot extractant is cooled, crystalline PbI<sub>2</sub> in high purity (> 95.9%) precipitated with a high yield: from glass-based perovskites, the first cycle of extraction / precipitation was sufficient to recover 94.4 ± 5.6% of Pb, whereas a second cycle yielded another 10.0 ± 5.2% Pb, making the recovery quantitative. The solid extraction residue remaining is consequently deprived of metals and may thus be disposed as non-hazardous waste. Therefore, exploiting the highly temperature-dependent solubility of PbI<sub>2</sub> in water provides a straightforward, easy to implement way to efficiently extract lead from PSC at the end-of-life and deposit the extraction residues in a cost-effective manner, mitigating the potential risk of lead leaching at the perovskites' end-of-life.