Solar-to-electricity conversion efficiency, power conversion efficiency (PCE), and stability are two important aspects of perovskite solar cells (PSCs). However, both aspects are difficult to simultaneously enhance. In the recent two years, two-dimensional (2D)/three-dimensional (3D) stacking structure, designed by covering the 3D perovskite with a thin 2D perovskite capping layer, was reported to be a promising method to achieve both a higher PCE and improved stability simultaneously. However, when reducing the surface defects of 3D perovskite, the thin 2D capping layer itself may probably introduce additional interfacial defects in a 2D/3D stacking structure, which is thought to be able to trigger trap-assisted nonradiative recombination or ion migration. Thus, efforts should be paid to reduce the interfacial defects of 2D hybrid perovskite when serving as a modification layer in a 2D/3D stacking structure PSCs. Here, we demonstrate that bromine (Br) doping of the 2D perovskite capping layer is an efficient strategy to passivate interfacial defects robustly, by which the photoluminescence lifetime is enhanced notably, whereas the interfacial charge recombination is suppressed a lot. As a result, the PCE is enhanced from 18.01% (3D perovskite) to 20.07% (Br-doped 2D/3D perovskite) along with improved moisture stability.
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http://dx.doi.org/10.1021/acsami.8b09461 | DOI Listing |
Environ Res
December 2024
School of Materials and Chemistry, Analytical and Testing Center, Innovation Center of Nuclear Environmental Safety Technology, Southwest University of Science and Technology, Mianyang, 621010, China. Electronic address:
In this work, a novel V-g-CN/BiVO (V-CN/BVO) Z-scheme heterojunction photocatalyst was formed by introducing nitrogen vacancies (V) and constructing heterojunction, which is able to efficiently degrade the representative contaminant rhodamine B (RhB) upon exposure to visible-light, resulting in an outstanding degradation rate of 98.91% of RhB within 30 min. This photocatalyst exhibits catalytic universality and allows the degradation of methylene blue (MB, 97.
View Article and Find Full Text PDFSmall
December 2024
State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, School of New Energy, North China Electric Power University, Beijing, 102206, China.
Incorporating chlorine into the SnO electron transport layer (ETL) has proven effective in enhancing the interfacial contact between SnO and perovskite in perovskite solar cells (PSCs). However, previous studies have primarily focused on the role of chlorine in passivating surface trap defects in SnO, without considering its influence on the buried interface. Here, hydrochloric acid (HCl) is introduced as a chlorine source into commercial SnO to form Cl-capped SnO (Cl-SnO) ETL, aiming to optimize the buried interface of the PSC.
View Article and Find Full Text PDFInorg Chem
December 2024
Department of Chemistry, National Institute of Technology, Rourkela 769008, Odisha, India.
Design of hierarchical hollow nanoheterostructure materials through interfacial and defect engineering is an innovative approach for achieving optimal charge separation dynamics and photon harvesting efficiency. Herein, we have described a facile technique to fabricate hollow MOF-derived C, N-doped-CoO (C, N-CoO) dodecahedral particles enwrapped with MgInS nanosheets for enhanced N reduction performance. ZIF-67 was initially used as a sacrificial template to prepare hollow C, N-CoO using a carbonization route followed by low-temperature calcination treatment.
View Article and Find Full Text PDFChem Sci
December 2024
Frontiers Science Center for Flexible Electronics (FSCFE), Institute of Flexible Electronics (IFE), Northwestern Polytechnical University Xi'an 710072 China
The interface between the perovskite layer and the electron transport layer is an extremely important factor that cannot be ignored in achieving high-performance perovskite photovoltaic technology. However, the void defects of the interface pose a serious challenge for high performance perovskite solar cells (PSCs). To address this, we report a polydentate ligand reinforced chelating strategy to strengthen the stability of the buried interface by managing interfacial defects and stress.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Chinese Academy of Sciences Dalian Institute of Chemical Physics, State Key Laboratory of Catalysis, CHINA.
Developing durably active catalysts to tackle harsh voltage polarization and seawater corrosion is pivotal for efficient solar-to-hydrogen (STH) conversion, yet remains a challenge. We report a durably active catalyst of NiCr-layered double hydroxide (RuldsNiCr-LDH) with highly exposed Ni-O-Ru units, in which low-loading Ru (0.32 wt%) is locked precisely at defect lattice site (Rulds) by Ni and Cr.
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