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Achieving a high open-circuit voltage in inverted wide-bandgap perovskite solar cells with a graded perovskite homojunction
摘要： Wide-bandgap (~1.7-1.8 eV) perovskite solar cells have attracted substantial research interest in recent years due to their great potential to fabricate efficient tandem solar cells via combining with a lower bandgap (1.1-1.3 eV) absorber (e.g., Si, copper indium gallium diselenide, or low-bandgap perovskite). However, wide-bandgap perovskite solar cells usually suffer from large open circuit voltage (Voc) deficits caused by small grain sizes and photoinduced phase segregation. Here, we demonstrate that in addition to large grain sizes and passivated grain boundaries, controlling interface properties is critical for achieving high Voc’s in the inverted wide-bandgap perovskite solar cells. We adopt guanidinium bromide solution to tune the effective doping and electronic properties of the surface layer of perovskite thin films, leading to the formation of a graded perovskite homojunction. The enhanced electric field at the perovskite homojunction is revealed by Kelvin probe force microscopy measurements. This advance enables an increase in the Voc of the inverted perovskite solar cells from an initial 1.12 V to 1.24 V. With the optimization of the device fabrication process, the champion inverted wide-bandgap cell delivers a power conversion efficiency of 18.19% and sustains more than 72% of its initial efficiency after continuous illumination for 70 h without encapsulation. Additionally, a semitransparent device with an indium tin oxide back contact retains more than 88% of its initial efficiency after 100 h maximum power point tracking.
关键词： wide-bandgap perovskite solar cells,perovskite homojunction,guanidinium bromide
更新于2025-10-22 19:40:53
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Highly Efficient and Stable GABr-Modified Ideal-Bandgap (1.35 eV) Sn/Pb Perovskite Solar Cells Achieve 20.63% Efficiency with a Record Small <i>V</i> <sub/>oc</sub> Deficit of 0.33 V
摘要： 1.5–1.6 eV bandgap Pb-based perovskite solar cells (PSCs) with 30–31% theoretical efficiency limit by the Shockley–Queisser model achieve 21–24% power conversion efficiencies (PCEs). However, the best PCEs of reported ideal-bandgap (1.3–1.4 eV) Sn–Pb PSCs with a higher 33% theoretical efficiency limit are <18%, mainly because of their large open-circuit voltage (Voc) deficits (>0.4 V). Herein, it is found that the addition of guanidinium bromide (GABr) can significantly improve the structural and photoelectric characteristics of ideal-bandgap (≈1.34 eV) Sn–Pb perovskite films. GABr introduced in the perovskite films can efficiently reduce the high defect density caused by Sn2+ oxidation in the perovskite, which is favorable for facilitating hole transport, decreasing charge-carrier recombination, and reducing the Voc deficit. Therefore, the best PCE of 20.63% with a certificated efficiency of 19.8% is achieved in 1.35 eV PSCs, along with a record small Voc deficit of 0.33 V, which is the highest PCE among all values reported to date for ideal-bandgap Sn–Pb PSCs. Moreover, the GABr-modified PSCs exhibit significantly improved environmental and thermal stability. This work represents a noteworthy step toward the fabrication of efficient and stable ideal-bandgap PSCs.
关键词： ideal bandgap,perovskite solar cells,mixed tin–lead perovskites,guanidinium bromide,molecular doping
更新于2025-09-23 15:21:01
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Highly luminescent and stable CH3NH3PbBr3 quantum dots with 91.7% photoluminescence quantum yield: Role of guanidinium bromide dopants
摘要： Although perovskite quantum dots (PQDs) have received considerable attention, defects in PQDs can significantly degrade the properties and device performance. In this study, we report on an effective strategy for synthesizing highly luminescent CH3NH3PbBr3 quantum dots (QDs) by a simple doping. To remove such defects, guanidinium bromide (GuBr) was doped into the CH3NH3PbBr3 QDs synthesized by the ligand-assisted reprecipitation technique. From XRD and TEM studies, the doping of GuBr into the QD lattices was verified. In addition, the surfaces of PQDs with and without GuBr dopants were analyzed by XPS to trace the metallic Pb acting as a major recombination center. The GuBr doping resulted in the size uniformity of QDs and effectively eliminated defects and metallic Pb, which enhanced the photoluminescence quantum yield (PLQY) through the inhibition of the non-radiative recombination pathway. Furthermore, the recombination dynamics in the QDs were examined by using time-resolved photoluminescence and fluorescence lifetime imaging to verify the role of GuBr dopants. By optimizing the amount of GuBr doping, the CH3NH3PbBr3 QDs with strong green emission achieved a maximum PLQY of 91.7%.
关键词： Photoluminescence quantum yield,Fluorescence lifetime imaging,CH3NH3PbBr3 quantum dots,Guanidinium bromide,Recombination centers
更新于2025-09-23 15:19:57