The efficiency of all-perovskite tandem devices falls far below theoretical efficiency limits, mainly because a widening bandgap fails to increase open-circuit voltage. We report on a bifacial all-perovskite tandem structures with an equivalent efficiency of 29.3% under back-to-front irradiance ratio of 30. This increases energy yield and reduces the required bandgap of a wide-bandgap cell. Open-circuit voltage deficit is therefore minimized, although its performance under only front irradiance is not ideal. The bifacial device needs a sputtered rear transparent electrode, which could reduce photon path length and deteriorate stability of Pb-Sn perovskites. Embedding a light-scattering micrometer-sized particle layer into perovskite to trap light, effectively increases absorptance by 5 to 15% in the infrared region. Using a nonacidic hole transport layer markedly stabilizes the hole-extraction interface by avoiding proton-accelerated formation of iodine. These two strategies together increase efficiency of semitransparent Pb-Sn cells from 15.6 to 19.4%, enabling fabrication of efficient bifacial all-perovskite tandem devices.
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http://dx.doi.org/10.1126/sciadv.add0377 | DOI Listing |
Nano Lett
December 2024
State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, China.
The performance of narrow-bandgap (NBG) perovskite solar cells (PSCs) is limited by the severe nonradiative recombination and carrier transport barrier at the electron selective interface. Here, we reveal the importance of the molecular orientation for effective defect passivation and protection for Sn at the perovskite/C interface. We constructed an internally self-anchored dual-passivation (ISADP) layer, where the orientation of PCBM can be significantly enhanced by the interaction between ammonium and carbonyl groups.
View Article and Find Full Text PDFSci Bull (Beijing)
December 2024
Key Lab for Special Functional Materials of Ministry of Education, National & Local Joint Engineering Research Center for High-efficiency Display and Lighting Technology, School of Nanoscience and Materials Engineering, and Collaborative Innovation Center of Nano Functional Materials and Applications, Henan University, Kaifeng 475004, China. Electronic address:
Mixed Sn-Pb perovskites are attracting significant attention due to their narrow bandgap and consequent potential for all-perovskite tandem solar cells. However, the conventional hole transport materials can lead to band misalignment or induce degradation at the buried interface of perovskite. Here we designed a self-assembled material 4-(9H-carbozol-9-yl)phenylboronic acid (4PBA) for the surface modification of the substrate as the hole-selective contact.
View Article and Find Full Text PDFChem Asian J
December 2024
Ningbo University, Department of Microelectronic Science and Engineering, Fenghua road 818, 315211, Ningbo, CHINA.
Mixed Tin-Lead perovskite solar cells (Sn-Pb PSCs) with a narrow band gap (NBG) are significant for single-junction and all-perovskite tandem solar cells due to their low toxicity and ideal band gap. Nevertheless, the performance and stability of the device are adversely affected by the uncontrollable crystallization and ion migration processes. Acetic acid (HAc) is introduced into the perovskite precursor solution as a multifunctional additive to enhance the film crystallization process and restrain ion migration in the device.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
School of Materials Science and Engineering, Kyungpook National University, Daegu, 41566, Republic of Korea.
Narrow-bandgap (NBG) Sn-Pb mixed perovskite solar cells (PSCs) represent a promising solution for surpassing the radiative efficiency of single-junction solar cells. The unique bandgap tunability of halide perovskites enables optimal tandem configurations of wide-bandgap (WBG) and NBG subcells. However, these devices are limited by the susceptibility of Sn in the NBG bottom cell to being oxidized to Sn, creating detrimental Sn vacancies.
View Article and Find Full Text PDFNanoscale
December 2024
Department of Physics, Faculty of Science, Srinakharinwirot University, Bangkok 10110, Thailand.
An all-perovskite tandem cell based on narrow-bandgap mixed tin-lead (Sn-Pb) alloyed perovskites is a potential photovoltaic device whose power conversion efficiency can exceed the Shockley-Queisser limit of a single-junction solar cell, 33%. However, comprehensive descriptions of the charge-carrier mobilities and transport mechanisms in the mixed Sn-Pb perovskite system remain elusive. Herein, we integrate density functional theory (DFT) calculations with charge transport models to provide more insight into the electronic structures and transport behaviors of these materials.
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