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    A sandwich-like structural model revealed for quasi-2D perovskite films
    Zheng, F ; Hall, CR ; Angmo, D ; Zuo, C ; Rubanov, S ; Wen, Z ; Bradley, SJ ; Hao, X-T ; Gao, M ; Smith, TA ; Ghiggino, KP (Royal Society of Chemistry, 2021-04-28)
    The excellent performance and stability of perovskite solar cells (PSCs) based on quasi-2D Ruddlesden–Popper perovskites (RPPs) holds promise for their commercialization. Further improvement in the performance of 2D PSCs requires a detailed understanding of the microstructure of the quasi-2D perovskite films. Based on scanning transmission electron microscopy (STEM), time-resolved photoluminescence, and transient absorption measurements, a new sandwich-like structural model is proposed to describe the phase distribution of RPPs. In contrast to the conventional gradient distribution, it is found that small-n RPPs are sandwiched between large-n RPP phase layers at the front and back sides owing to crystallization initiated from both interfaces during film formation. This sandwich-like distribution profile facilitates excitons funneling from the film interior to both surfaces for dissociation while free carriers transport via large-n channels that permeate the film to ensure efficient charge collection by the corresponding electrodes, which is favorable for high-performance photovoltaics. This discovery provides a new fundamental understanding of the operating principles of 2D PSCs and has valuable implications for the design and optimization strategies of optoelectronic devices based on quasi-2D RPPs films.
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    Brownian Tree‐Shaped Dendrites in Quasi‐2D Perovskite Films and Their Impact on Photovoltaic Performance
    Zheng, F ; Angmo, D ; Hall, CR ; Rubanov, S ; Yuan, F ; Laird, JS ; Gao, M ; Smith, TA ; Ghiggino, KP (Wiley, 2022-05)
    Quasi-2D Ruddlesden–Popper perovskites (RPPs) are candidates for constructing perovskite solar cells (PSCs) with superior stability due to their tolerance to the external environment. Fully understanding the film growth mechanism and structure is crucial to further improve the performance of 2D-PSCs while maintaining device stability. In this work, the origin of Brownian tree-shaped dendrites formed in hot-cast methylammonium chloride (MACl)-doped BA2MAn−1PbnI3n+1 ( = 5) quasi-2D perovskite films are reported. Investigations based on optical, electronic, atomic force, and fluorescence microscopies reveal that the dendrites are assembled from large-n RPPs-dominated grains, while the nondendritic film area is composed of small-n RPPs grains and associated with film surface pits caused by the evaporation of MACl. It is proposed that these dendrites are grown by the diffusion-limited aggregation of the MA-rich intermediate phase domains that initially crystallize from the precursor. The formation of these dendrites in quasi-2D perovskite films upon MACl doping is accompanied by improved organization and crystallinity of the 2D RPPs, which benefits the photovoltaic performance. This work provides new insights into the formation mechanism of quasi-2D perovskite films that should assist device engineering strategies to further improve the performance of 2D PSCs.
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    Spontaneous Formation of a Ligand-Based 2D Capping Layer on the Surface of Quasi-2D Perovskite Films
    Zheng, F ; Raeber, T ; Rubanov, S ; Lee, C ; Seeber, A ; Hall, C ; Smith, TA ; Gao, M ; Angmo, D ; Ghiggino, KP (AMER CHEMICAL SOC, 2022-11-23)
    Two-dimensional (2D) Ruddlesden-Popper phase perovskites (RPPs) are attracting growing attention for photovoltaic applications due to their enhanced stability compared to three-dimensional (3D) perovskites. The superior tolerance of 2D RPPs films to moisture and oxygen is mainly attributed to the hydrophobic nature of the introduced long-chain spacer cations (ligands). In this work, it is revealed that a thin capping layer, consisting of self-assembled butylammonium ligands, is spontaneously formed on the top surface of a quasi-2D perovskite film prepared by conventional one-step hot casting. Based on morphological and crystallographic analyses of both the top/bottom surfaces and the interior of quasi-2D perovskite films, the formation process of the 2D capping layer and the assembly of RPPs, comprising both large and small slab thickness (large-n, small-n), is elucidated. The vertical orientation of RPPs that is required for sufficient charge transport for 2D perovskite solar cells (PSCs) is further verified. We propose that the surface capping layer is directly responsible for the long-term stability of 2D PSCs. This work provides detailed insight into the microstructure of quasi-2D RPPs films that should assist the development of strategies for unlocking the full potential of 2D perovskites for high-performance PSCs and other solid-state electronic devices.
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    Brownian Tree-Shaped Dendrites in Quasi-2D Perovskite Films and Their Impact on Photovoltaic Performance
    Zheng, F ; Angmo, D ; Hall, CR ; Rubanov, S ; Yuan, F ; Laird, JS ; Gao, M ; Smith, TA ; Ghiggino, KP (WILEY, 2022-05)
    Abstract Quasi‐2D Ruddlesden–Popper perovskites (RPPs) are candidates for constructing perovskite solar cells (PSCs) with superior stability due to their tolerance to the external environment. Fully understanding the film growth mechanism and structure is crucial to further improve the performance of 2D‐PSCs while maintaining device stability. In this work, the origin of Brownian tree‐shaped dendrites formed in hot‐cast methylammonium chloride (MACl)‐doped BA2MAn−1PbnI3n+1 (<n> = 5) quasi‐2D perovskite films are reported. Investigations based on optical, electronic, atomic force, and fluorescence microscopies reveal that the dendrites are assembled from large‐n RPPs‐dominated grains, while the nondendritic film area is composed of small‐n RPPs grains and associated with film surface pits caused by the evaporation of MACl. It is proposed that these dendrites are grown by the diffusion‐limited aggregation of the MA‐rich intermediate phase domains that initially crystallize from the precursor. The formation of these dendrites in quasi‐2D perovskite films upon MACl doping is accompanied by improved organization and crystallinity of the 2D RPPs, which benefits the photovoltaic performance. This work provides new insights into the formation mechanism of quasi‐2D perovskite films that should assist device engineering strategies to further improve the performance of 2D PSCs.
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    The role of conformational heterogeneity in the excited state dynamics of linked diketopyrrolopyrrole dimers†
    Bradley, SJ ; Chi, M ; White, JM ; Hall, CR ; Goerigk, L ; Smith, TA ; Ghiggino, KP (ROYAL SOC CHEMISTRY, 2021-04-21)
    Diketopyrrolopyrrole (DPP) derivatives have been proposed for both singlet fission and energy upconversion as they meet the energetic requirements and exhibit superior photostability compared to many other chromophores. In this study, both time-resolved electronic and IR spectroscopy have been applied to investigate excited state relaxation processes competing with fission in dimers of DPP derivatives with varying linker structures. A charge-separated (CS) state is shown to be an important intermediate with dynamics that are both solvent and linker dependent. The CS state is found for a subset of the total population of excited molecules and it is proposed that CS state formation requires suitably aligned dimers within a broader distribution of conformations available in solution. No long-lived triplet signatures indicative of singlet fission were detected, with the CS state likely acting as an alternative relaxation pathway for the excitation energy. This study provides insight into the role of molecular conformation in determining excited state relaxation pathways in DPP dimer systems.
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    Highly efficient radiative recombination in intrinsically zero-dimensional perovskite micro-crystals prepared by thermally-assisted solution-phase synthesis
    Xu, W-L ; Bradley, SJ ; Xu, Y ; Zheng, F ; Hall, CR ; Ghiggino, KP ; Smith, TA (ROYAL SOC CHEMISTRY, 2020-12-07)
    Zero-dimensional (0D) quantum confinement can be achieved in perovskite materials by the confinement of electron and hole states to single PbX6 4- perovskite octahedra. In this work, 0D perovskite (Cs4PbBr6) micro-crystals were prepared by a simple thermally-assisted solution method and thoroughly characterized. The micro-crystals show a high level of crystallinity and a high photoluminescence quantum yield of 45%. The radiative recombination coefficient of the 0D perovskite micro-crystals, 1.5 × 10-8 s-1 cm3, is two orders of magnitude higher than that of typical three-dimensional perovskite and is likely a strong contributing factor to the high emission efficiency of 0D perovskite materials. Temperature dependent luminescence measurements provide insight into the role of thermally-activated trap states. Spatially resolved measurements on single 0D perovskite micro-crystals reveal uniform photoluminescence intensity and emission decay behaviour suggesting the solution-based fabrication method yields a high-quality and homogenous single-crystal material. Such uniform emission reflects the intrinsic 0D nature of the material, which may be beneficial to device applications.