98%
921
2 minutes
20
Realization of a high-quality back electrode interface (BEI) with suppressed recombination is crucial for CuZnSn(S,Se) (CZTSSe) solar cells. To achieve this goal, the construction of a traditional chemical passivation effect has been widely adopted and investigated. However, there is currently a lack of reports concerning the construction of a field passivation effect (FPE) for the BEI. Herein, considering the characteristic of the negligible difference in ionic radius between Mo (0.65 Å) and V (0.64 Å) as well as the presence of one less valence electron compared to Mo, vanadium (V) was employed and incorporated into the MoSe interfacial layer during the deposition of the Mo:V electrode and selenization process. This allowed for the establishment of a desirable VI-FPE interface with p-MoSe:V/p-CZTSSe at the BEI. The p-type characteristic in MoSe:V is attributed to the presence of the V acceptor; notably, the Fermi energy level of MoSe:V has shifted downward by 0.62 eV compared to MoSe, thereby facilitating the formation of an optimized band alignment between MoSe:V and the absorber. Consequently, the photovoltaic parameters of the cell-FPE have experienced a significant increase due to the enhanced carrier transportation efficiency compared to cell-ref, resulting in a remarkable improvement in efficiency from 8.28 to 11.11%.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.4c09508 | DOI Listing |
Adv Mater
September 2025
Key Lab of Artificial Micro- and Nano-Structures of Ministry of Education of China, School of Physics and Technology, Wuhan University, Wuhan, 430072, China.
Sequential deposition technique is widely used to fabricate perovskite films with large grain size in perovskite solar cells (PSCs). Residual lead halide (PbI) in the perovskite film tends to be decomposed into metallic lead (Pb) under long-term heating or light soaking. Here, a chiral levetiracetam (LEV) dopant containing α-amide and pyrrolidone groups is introduced into the PbI precursor solution.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Nanoelectronics Graphene and 2D Materials Laboratory, CITIC-UGR, Department of Electronics, University of Granada, Granada 18014, Spain.
The relentless scaling of semiconductor technology demands materials beyond silicon to sustain performance improvements. Transition metal dichalcogenides (TMDs), particularly MoS, offer excellent electronic properties; however, achieving scalable and CMOS-compatible fabrication remains a critical challenge. Here, we demonstrate a scalable and BEOL-compatible approach for the direct wafer-scale growth of MoS devices using plasma-enhanced atomic layer deposition (PE-ALD) at temperatures below 450 °C, fully compliant with CMOS thermal budgets.
View Article and Find Full Text PDFAnal Chem
September 2025
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, Jiangsu 213164, P. R. China.
Rational design of both mechanistic pathways and material compositions is essential to advance COF-based electrochemiluminescence (ECL) systems. In this study, aggregation-induced emission covalent organic framework (AIE-COF) nanoprobes with excellent ECL performance were developed based on Tb-functionalized covalent organic framework (Tb@A-COF). The Tb@A-COF system demonstrates enhanced ECL performance through synergistic integration of three complementary mechanisms: (1) (4',4',4',4'-(1,2-ethenediylidene)tetrakis [1,1'-biphenyl]-4-carboxaldehyde (ETBC) ligands function as antenna-like sensitizers that amplify luminescence intensity by 14.
View Article and Find Full Text PDFRSC Adv
August 2025
Engineering Research Center for Nanomaterials, The First Affiliated Hospital, The Academy for Advanced Interdisciplinary Studies, College of Chemistry and Molecular Sciences, Henan University Zhengzhou 450046 China
Nanoscale zero-valent iron (nZVI) was synthesized by a one-pot liquid-phase chemical method in the presence of FeSO as the iron source and NaBH as the reducing agent. The synthesized nZVI was characterized by scanning electron microscopy, X-ray diffraction, energy dispersive spectrometry, and Fourier transform infrared spectroscopy. Its ability to passivate Pb, Cd, and AsO in soils was evaluated by inductively coupled plasma-atomic emission spectroscopy, and the passivation mechanism was explored based on adsorption thermodynamics and kinetics simulations.
View Article and Find Full Text PDF