研究目的
To improve the resistive memory properties of a PEDOT:PSS/MAPbI3-based device by using potassium iodide (KI) additives to enhance film quality and interface properties.
研究成果
KI additives improve the memory properties of PEDOT:PSS/MAPbI3-based devices by enhancing film quality and passivating defects, leading to higher ON/OFF ratios, better endurance, and stable retention. Optimal doping (5 mg/ml) provides significant improvements, suggesting KI's potential for high-performance perovskite memory devices. Future work should focus on defect control and mechanism elucidation.
研究不足
The mechanism of resistive switching is complex and dependent on structure and process parameters. Endurance and retention properties vary with KI doping amount, and excessive doping degrades performance. The study is limited to specific device structures and materials, and scalability to practical applications may require further optimization.
1:Experimental Design and Method Selection:
A nonvolatile memory device with a structure of Glass/ITO/PEDOT:PSS/MAPbI3/PMMA/Al was fabricated. The MAPbI3 film was prepared using a two-step sequential process (PbI2 layer + MAI conversion). KI was added to the PbI2 precursor to study its doping effect on memory properties.
2:Sample Selection and Data Sources:
ITO-coated glass substrates were used. Materials included PbI2, KI, DMF, IPA, CB, PMMA, PEDOT:PSS, and MAI purchased from specified suppliers.
3:List of Experimental Equipment and Materials:
Equipment included an ultrasonic cleaner, oven, N2-filled glove box, spin coater, hot plate, thermal evaporator, HR-SEM (Hitachi SU8000), XRD (Bruker D8 Advance), photoluminescence spectrometer (Horiba Jobin Yvon LabRAM HR), XPS (ULVAC-PHI Quantera SXM), and I-V measurement system (Agilent E5270B). Materials: PbI2 (
4:9985%), KI (995%), DMF (8%), IPA (5%), CB (8%), PMMA, PEDOT:
PSS, MAI (>98%).
5:Experimental Procedures and Operational Workflow:
Substrates were cleaned and dried. PEDOT:PSS was spin-coated and baked. KI-doped PbI2 precursor was prepared and spin-coated, then baked. MAI/IPA was spin-coated and annealed to form MAPbI3, followed by washing with IPA and further annealing. PMMA was spin-coated and baked. Al top electrode was deposited by thermal evaporation.
6:Data Analysis Methods:
Surface morphology was analyzed by SEM, crystalline phase by XRD, photoluminescence by spectrometer, element distribution by XPS, and I-V characteristics by Agilent E5270B. Conduction mechanisms were fitted using SCLC and Ohmic models.
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Scanning Electron Microscope
SU8000
Hitachi
Investigate surface morphologies of the films
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X-ray Diffractometer
D8 Advance
Bruker
Characterize crystalline phase of the films
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I-V Measurement System
E5270B
Agilent
Measure current-voltage characteristics
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Photoluminescence Spectrometer
LabRAM HR
Horiba Jobin Yvon
Record steady-state photoluminescence spectra
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X-ray Photoelectron Spectrometer
Quantera SXM
ULVAC-PHI
Perform XPS depth analysis
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Lead Iodide
Alfa Aesar
Precursor material for MAPbI3 film
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Potassium Iodide
Alfa Aesar
Additive for improving film quality
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N,N-Dimethylformamide
Sigma-Aldrich
Solvent for precursors
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2-Propanol
Sigma-Aldrich
Solvent for MAI precursor
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Chlorobenzene
Sigma-Aldrich
Solvent for PMMA solution
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Poly(methyl methacrylate)
Sigma-Aldrich
Buffer layer in the device
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Poly(3,4-ethylenedioxythiophene) polystyrene sulfonate
Uni-onward
Hole transporting layer
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Methylammonium Iodide
Uni-onward
Precursor for MAPbI3 formation
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