In this work, a lithium and silver co-doping strategy has been successfully implied to prepare NiO films for high performance inverted planar perovskite solar cells (PSCs). Compared to the pristine and single-doped NiO , the Li and Ag co-doping approach exhibits the synergistic effect and can endow NiO films with higher electrical conductivity, higher hole mobility and better interface energy band alignment with perovskite active layers. Moreover, the perovskite film with enhanced crystallinity can be obtained induced by the Li,Ag:NiO film. The PSC with Li,Ag:NiO HTL shows a high power conversion efficiency (PCE) up to 19.24% and less hysteresis effect, which outperforms the devices with the pristine NiO or single-doped NiO HTLs. Meanwhile, the Li,Ag:NiO device can retain 95% of its initial PCE after storage at the relative humidity of 30 ± 2% in 30 days without encapsulation. Our work demonstrates that lithium and silver co-doping is a promising route for realizing efficient p-type NiO HTL, which provides a simple way to boost the efficient and stable of inverted planar PSCs.
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http://dx.doi.org/10.1021/acsami.8b16649 | DOI Listing |
J Chem Theory Comput
January 2025
Department of Chemistry, Brandeis University, 415 South Street, Waltham, Massachusetts 02453, United States.
The photocatalytic efficiency of materials such as graphene and noble metal nanoclusters depends on their plasmon lifetimes. Plasmon dephasing and decay in these materials is thought to occur on ultrafast time scales, ranging from a few femtoseconds to hundreds of femtoseconds and longer. Here we focus on understanding the dephasing and decay pathways of excited states in small lithium and silver clusters and in plasmonic states of the π-conjugated molecule anthracene, providing insights that are crucial for interpreting optical properties and photophysics.
View Article and Find Full Text PDFNanomaterials (Basel)
December 2024
Quantum Nano Centre, Department of Chemical Engineering, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Laser conversion of commercial polymers to laser-induced graphene (LIG) using inexpensive and accessible CO lasers has enabled the rapid prototyping of promising electronic and electrochemical devices. Frequently used to pattern interdigitated supercapacitors, few approaches have been developed to pattern batteries-in particular, full cells. Herein, we report an LIG-based approach to a planar, interdigitated Li-S battery.
View Article and Find Full Text PDFLuminescence
January 2025
Vlokh Institute of Physical Optics, Ivan Franko National University of Lviv, Lviv, Ukraine.
Spectroscopic properties of Tb-doped and Tb-Ag codoped lithium tetraborate (LTB) glasses with LiBO (or LiO-2BO) composition are investigated and analysed using electron paramagnetic resonance (EPR), optical absorption, photoluminescence (PL) and photoluminescence excitation (PLE) spectra, PL decay kinetics and absolute quantum yield (QY) measurements. PL spectra of the investigated glasses show numerous narrow emission bands corresponding to the D → F (J = 6-0) and D → F (J = 5-3) transitions of Tb (4f) ions. The most intense PL band of Tb ions at 541 nm (D → F transition) is characterised by a lifetime slightly exceeding 2.
View Article and Find Full Text PDFChemphyschem
January 2025
Stony Brook University, Chemistry, Department of Chemistry, Stony Brook University, 11794, Stony Brook, UNITED STATES OF AMERICA.
For batteries to function effectively all active material must be accessible requiring both electron and ion transport to each particle. A common approach to generating the needed conductive network is the addition of carbon. An alternative approach is the electrochemically induced formation of conductive reaction products generated with intimate contact to the active material.
View Article and Find Full Text PDFNat Mater
January 2025
Department of Mechanical Engineering, The Pennsylvania State University, University Park, PA, USA.
Lithium-sulfur (Li-S) all-solid-state batteries (ASSBs) hold great promise for next-generation safe, durable and energy-dense battery technology. However, solid-state sulfur conversion reactions are kinetically sluggish and primarily constrained to the restricted three-phase boundary area of sulfur, carbon and solid electrolytes, making it challenging to achieve high sulfur utilization. Here we develop and implement mixed ionic-electronic conductors (MIECs) in sulfur cathodes to replace conventional solid electrolytes and invoke conversion reactions at sulfur-MIEC interfaces in addition to traditional three-phase boundaries.
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