To achieve the full potential of monolithic perovskite/silicon tandem solar cells, crystal defects and film inhomogeneities in the perovskite top cell must be minimized. We discuss the use of methylenediammonium dichloride as an additive to the perovskite precursor solution, resulting in the incorporation of in situ-formed tetrahydrotriazinium (THTZ-H) into the perovskite lattice upon film crystallization. The cyclic nature of the THTZ-H cation enables a strong interaction with the lead octahedra of the perovskite lattice through the formation of hydrogen bonds with iodide in multiple directions. This structure improves the device power conversion efficiency (PCE) and phase stability of 1.68 electron volts perovskites under prolonged light and heat exposure under 1-sun illumination at 85°C. Monolithic perovskite/silicon tandems incorporating THTZ-H in the perovskite photo absorber reached a 33.7% independently certified PCE for a device area of 1 square centimeter.
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http://dx.doi.org/10.1126/science.adp1621 | DOI Listing |
ACS Nano
December 2024
Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, Guangdong Basic Research Center of Excellence for Energy & Information Polymer Materials, South China University of Technology, Guangzhou 510640, P. R. China.
Perovskite/organic tandem solar cells (PO-TSCs) have recently attracted increasing attention due to their high efficiency and excellent stability. The interconnecting layer (ICL) is of great importance for the performance of PO-TSCs. The charge transport layer (CTL) and the charge recombination layer (CRL) that form the ICL should be carefully designed to enhance charge carrier extraction and promote charge carrier recombination balance from the two subcells.
View Article and Find Full Text PDFNano 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 PDFSmall
December 2024
Photovoltaic Materials Group, Center for GREEN Research on Energy and Environmental Materials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.
Surface passivation with multifunctional molecules is an effective strategy to mitigate the defect and improve the performance and stability of perovskite solar cells (PSCs). Here, the fabrication of a wide bandgap-PSC is reported with tin perovskite (WB-Sn-HP; bandgap: 1.68 eV), followed by molecular surface passivation using 4-Fluoro-benzohydrazide (F-BHZ).
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