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  • Physics  (2)
  • 1
    In: Applied Physics Letters, AIP Publishing, Vol. 115, No. 25 ( 2019-12-16)
    Abstract: In this letter, a series of vanadium dioxide (VO2) epitaxial films were deliberately deposited on TiO2 substrates with different orientations [(001), (110), and (101)], in an attempt to gain insights into the strained VO2 epitaxial film. We found in-plane [100] and [1-10] directions, obviously anisotropic metal-insulator transition (MIT) in (110)-oriented VO2 films. In combination with synchrotron radiation high-resolution x-ray diffraction characterizations, electronic transport data reveal that the critical temperature of MIT depends on the strain state of the dimeric vanadium atomic chain along the c axis of the rutile phase. The anisotropy of MIT is closely related to the orientation of the VO2 films, which is caused by the varied orientation configuration of V-V atomic chain dimerization in the films. Soft x-ray absorption spectroscopy results further indicate that this anisotropy may be driven by the directional hybridization of O 2p and V 3d orbitals with respect to the orientation of VO2 thin films. The polarization-dependent V L-edge and O K-edge XAS data suggest that the elongation of the apical V-O bond length increases the p-d orbital overlap; thus, the energy level of the d// orbital is raised relative to that of the π* orbital. These anisotropic MIT behaviors will help us to understand how the strain engineering depends on the strain state of vanadium dimers in VO2 films.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2019
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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  • 2
    In: Advanced Materials, Wiley, Vol. 34, No. 40 ( 2022-10)
    Abstract: Here, the authors report a highly efficient integrated ideal‐bandgap perovskite/bulk‐heterojunction solar cell (IPBSC) with an inverted architecture, featuring a near infrared (NIR) polymer DTBTI‐based bulk‐heterojunction (BHJ) layer atop guanidinium bromide (GABr)‐modified FA 0.7 MA 0.3 Pb 0.7 Sn 0.3 I 3 perovskite film as the photoactive layer. The IPBSC shows cascade‐like energy level alignment between the charge‐extractionlayer/perovskite/BHJ and efficient passivation effect of BHJ on perovskite. Thanks to the well‐matched energy level alignment and high‐quality ideal bandgap‐based perovskite film, an efficient charge transfer occurs between the charge‐extraction‐layer/perovskite/BHJ. Moreover, the NIR polymer DTBTI on the perovskite film leads to an improved NIR light response for the IPBSC. In addition, the O, S and N atoms in the DTBTI polymer yield a strong interaction with perovskite, which is conducive to reducing the defects of the perovskite and suppressing charge recombination. As a result, the solar cell achieves a power conversion efficiency (PCE) of 24.27% (certificated value at 23.4% with 0.283‐volt voltage loss), currently the recorded efficiency for both IPBSCs and Pb‐Sn alloyed PSCs, and which is over the highest efficiency of perovskite–organic tandem solar cell. Moreover, the thermal, humidity and long‐term operational stabilities of the IPBSCs are also significantly improved compared with the control PSCs.
    Type of Medium: Online Resource
    ISSN: 0935-9648 , 1521-4095
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1474949-X
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