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To achieve high power conversion efficiency in perovskite/silicon tandem solar cells, it is necessary to develop a promising wide-bandgap perovskite absorber and processing techniques in relevance. To date, the performance of devices based on wide-bandgap perovskite is still limited mainly by carrier recombination at their electron extraction interface. Here, we demonstrate assembling a binary two-dimensional perovskite by both alternating-cation-interlayer phase and Ruddlesden-Popper phase to passivate perovskite/C interface. The binary two-dimensional strategy takes effects not only at the interface but also in the bulk, which enables efficient charge transport in a wide-bandgap perovskite solar cell with a stabilized efficiency of 20.79% (1 cm). Based on this absorber, a monolithic perovskite/silicon tandem solar cell is fabricated with a steady-state efficiency of 30.65% assessed by a third party. Moreover, the tandem devices retain 96% of their initial efficiency after 527 h of operation under full spectral continuous illumination, and 98% after 1000 h of damp-heat testing (85 °C with 85% relative humidity).
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http://dx.doi.org/10.1038/s41467-024-51345-2 | DOI Listing |
J Colloid Interface Sci
September 2025
School of Materials Science and Engineering, Taizhou University, Taizhou 318000, China. Electronic address:
The sequential preparation of perovskite solar cells (PSCs) has received widespread concern for its use in large-scale perovskite modules and perovskite/silicon tandem solar cells. However, the instability of the PbI precursor solution and the incomplete reaction of ammonium salts hinder the industrialization of PSCs. Here, by introducing phthalamide (PA) into PbI solution, the carbonyl oxygen of PA molecules undergoes a bidentate coordination reaction with Pb to form an octahedral coordination structure, and the nitrogen atom in the -NH group exhibits weakly acidic properties due to the conjugation effect.
View Article and Find Full Text PDFSmall Methods
September 2025
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, Republic of Korea.
Monolithic perovskite/silicon tandem (PST) solar cells are rapidly emerging as next-generation solar cells with significant potential for commercialization. This study presents a proof of concept for a silicon diffused junction-based PST cell, utilizing a passivated emitter rear contact (PERC) cell with a low-temperature (<200 °C) laser-fired contact process to minimize thermal damage. By introducing amorphous silicon to the emitter surface of PERC bottom cell, the open circuit voltage (V) improve from 0.
View Article and Find Full Text PDFChemSusChem
August 2025
Institute of Photovoltaics, School of Physics and Materials Science, Nanchang University, Nanchang, 330031, China.
As the pursuit for cost reduction of photovoltaic technologies goes on, the interest in high-efficiency Si-tandem solar cells has been strongly increasing, among which perovskite/silicon has demonstrated impressive results and prospects for further enhancements. However, the existence of deleterious defects at the surface of wide-bandgap perovskite films in the top solar cells dramatically impedes the potential industrial applications of perovskite/silicon tandem solar cells. In this review, begin by summarizing the various types of defects and the passivation mechanisms to provide guidance for the passivation protocols.
View Article and Find Full Text PDFNat Commun
August 2025
State Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy, State Key Laboratory of Chemical Reaction Dynamics, Dalian Institute of Chemical Physics, Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Dalian, Liaoning, China.
The perovskite/silicon tandem solar cells (TSCs) offers a state-of-the-art solution for achieving unparalleled efficiency and cost-effectiveness in solar energy conversion. However, the fabrication of high-quality wide-bandgap perovskite films with a thickness of 1 μm on nano-textured silicon substrates remains a formidable challenge. Herein, we designed an amphoteric coplanar conjugated molecule (ACCM) guided by the principles of density functional theory and Brønsted acid-base chemistry.
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