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    Amassian, Aram (2)
    Beaujuge, Pierre (1)Dey, Sukumar (1)El Labban, Abdulrahman (1)Firdaus, Yuliar (1)View MoreDepartmentKAUST Solar Center (KSC) (2)
    Materials Science and Engineering Program (2)
    Physical Sciences and Engineering (PSE) Division (2)
    Advanced Membranes and Porous Materials Research Center (1)Chemical and Biological Engineering Program (1)View MoreJournalACS Energy Letters (1)ACS Nano (1)KAUST Grant NumberURF/1/1723 (1)URF/1/2570-01-01 (1)URF/1/2634-01 (1)Publisher
    American Chemical Society (ACS) (2)
    Subjectcoordination polymers (1)lithium−sulfur battery (1)polysulfide (1)shuttling effect (1)two-dimensional materials (1)View MoreTypeArticle (2)Year (Issue Date)
    2018 (2)
    Item AvailabilityMetadata Only (1)Open Access (1)

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    Hybrid Tandem Quantum Dot/Organic Solar Cells with Enhanced Photocurrent and Efficiency via Ink and Interlayer Engineering

    Kim, Taesoo; Firdaus, Yuliar; Kirmani, Ahmad R.; Liang, Ru-Ze; Hu, Hanlin; Liu, Mengxia; El Labban, Abdulrahman; Hoogland, Sjoerd; Beaujuge, Pierre; Sargent, Edward H.; Amassian, Aram (ACS Energy Letters, American Chemical Society (ACS), 2018-05-03) [Article]
    Realization of colloidal quantum dot (CQD)/organic photovoltaic (OPV) tandem solar cells that integrate the strong infrared absorption of CQDs with large photovoltages of OPVs is an attractive option toward high-performing, low-cost thin film solar cells. To date, monolithic hybrid tandem integration of CQD/OPV solar cells has been restricted due to the CQD ink’s catastrophic damage to the organic subcell, thus forcing the low bandgap CQD to be used as front cell. This sub-optimal configuration limits the maximum achievable photocurrent in CQD/OPV hybrid tandem solar cells. In this work, we demonstrate hybrid tandem solar cells employing a low-bandgap CQD back cell on top of an organic front cell thanks to a modified CQD ink formulation and a robust interconnection layer (ICL) which together overcome the long-standing integration challenges for CQD and organic subcells. The resulting tandem architecture surpasses previously reported current densities by ~20-25% and yields a state-of-the-art power conversion efficiency (PCE) of 9.4%.
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    Functional Two-Dimensional Coordination Polymeric Layer as a Charge Barrier in Li–S Batteries

    Huang, Jing-Kai; Li, Mengliu; Wan, Yi; Dey, Sukumar; Ostwal, Mayur; Zhang, Daliang; Yang, Chih-Wen; Su, Chun-Jen; Jeng, U-Ser; Ming, Jun; Amassian, Aram; Lai, Zhiping; Han, Yu; Li, Sean; Li, Lain-Jong (ACS Nano, American Chemical Society (ACS), 2018-01-08) [Article]
    Ultrathin two-dimensional (2D) polymeric layers are capable of separating gases and molecules based on the reported size exclusion mechanism. What is equally important but missing today is an exploration of the 2D layers with charge functionality, which enables applications using the charge exclusion principle. This work demonstrates a simple and scalable method of synthesizing a free-standing 2D coordination polymer Zn2(benzimidazolate)2(OH)2 at the air–water interface. The hydroxyl (−OH) groups are stoichiometrically coordinated and implement electrostatic charges in the 2D structures, providing powerful functionality as a charge barrier. Electrochemical performance of the Li–S battery shows that the Zn2(benzimidazolate)2(OH)2 coordination polymer layers efficiently mitigate the polysulfide shuttling effects and largely enhance the battery capacity and cycle performance. The synthesis of the proposed coordination polymeric layers is simple, scalable, cost saving, and promising for practical use in batteries.
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