Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/118538
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Physics | - |
| dc.creator | Qiu, J | - |
| dc.creator | Zhu, H | - |
| dc.creator | Shao, B | - |
| dc.creator | Shi, Y | - |
| dc.creator | Xu, S | - |
| dc.creator | Abulikemu, M | - |
| dc.creator | Liu, J | - |
| dc.creator | Zheng, Z | - |
| dc.creator | Jamal, A | - |
| dc.creator | Alsaiari, HA | - |
| dc.creator | Aqeel, S | - |
| dc.creator | Gereige, I | - |
| dc.creator | Zhang, F | - |
| dc.creator | Yin, J | - |
| dc.creator | Li, C | - |
| dc.creator | Bakr, OM | - |
| dc.date.accessioned | 2026-04-20T07:19:52Z | - |
| dc.date.available | 2026-04-20T07:19:52Z | - |
| dc.identifier.issn | 0002-7863 | - |
| dc.identifier.uri | http://hdl.handle.net/10397/118538 | - |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.title | Tailored electron-deficient macrocycles guiding the perovskite crystallization process for solar cells | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 42061 | - |
| dc.identifier.epage | 42069 | - |
| dc.identifier.volume | 147 | - |
| dc.identifier.issue | 45 | - |
| dc.identifier.doi | 10.1021/jacs.5c15639 | - |
| dcterms.abstract | Perovskite solar cells (PSCs) exhibit impressive power conversion efficiencies (PCEs), but their stability still falls short of industrial commercialization requirements, primarily due to inherent defects and halide ion migration within the perovskite materials. To address this shortcoming, we developed a novel electron-deficient biphen[n]arene macrocycle molecule, NBP[2], synthesized through the condensation of the monomer 2,2″,4,4″-tetramethoxy-4’,6’-dinitro-1,1’:3′,1″-terphenyl (NP) with paraformaldehyde. When the macrocyclic molecule is introduced into the perovskite film via the antisolvent injection method, it functions as a regulator of the crystallization process of perovskite and an inhibitor of halide anion migration. In addition, NBP[2] can effectively bind with uncoordinated halide ions and Pb²⁺, reducing intrinsic defects through Lewis acid–base and cation−π interactions. As a result, NBP[2]-modified PSCs achieve a PCE of up to 25.38% (compared to 23.89% for the control) and retain 95.8% of their initial efficiency after 1000 h of maximum power point tracking under 1-sun illumination at room temperature in an N₂ atmosphere. | - |
| dcterms.accessRights | embargoed access | en_US |
| dcterms.bibliographicCitation | Journal of the American Chemical Society, 12 Nov. 2025, v. 147, no. 45, p. 42061-42069 | - |
| dcterms.isPartOf | Journal of the American Chemical Society | - |
| dcterms.issued | 2025-11-12 | - |
| dc.identifier.scopus | 2-s2.0-105021306013 | - |
| dc.identifier.pmid | 41152154 | - |
| dc.identifier.eissn | 1520-5126 | - |
| dc.description.validate | 202604 bcjz | - |
| dc.description.oa | Not applicable | en_US |
| dc.identifier.SubFormID | G001457/2026-01 | en_US |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | J. Q, S. X., Z. Z., and C. L acknowledge funding support from the National Natural Science Foundation of China (22301218) and the Natural Science Foundation of Tianjin City (23JCZDJC00660). B.S. thanks funding support from the China Scholarship Council (No. 202006070004). J.Y. acknowledges financial support from National Natural Science Foundation of China (62422512), Hong Kong Polytechnic University (Grant no. P0053682) and a grant from the Research Grants Council of the Hong Kong Special Administrative Region, China (Project No. 15300724). This work was supported by Saudi Aramco and King Abdullah University of Science and Technology (KAUST). We also acknowledge the Supercomputing Laboratory at KAUST for the computational resources. | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.date.embargo | 2026-10-28 | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
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