The high open-circuit voltage (V ) loss arising from insufficient surface passivation is the main factor that limits the efficiency of current lead sulfide colloidal quantum dots (PbS CQDs) solar cell. Here, synergistic passivation is performed in the direct synthesis of conductive PbS CQD inks by introducing multifunctional ligands to well coordinate the complicated CQDs surface with the thermodynamically optimal configuration. The improved passivation effect is intactly delivered to the final photovoltaic device, leading to an order lower surface trap density and beneficial doping behavior compared to the control sample. The obtained CQD inks show the highest photoluminescence quantum yield (PLQY) of 24% for all photovoltaic PbS CQD inks, which is more than twice the reported average PLQY value of ≈10%. As a result, a high V of 0.71 V and power conversion efficiency (PCE) of 13.3% is achieved, which results in the lowest V loss (0.35 eV) for the reported PbS CQD solar cells with PCE >10%, comparable to that of perovskite solar cells. This work provides valuable insights into the future CQDs passivation strategies and also demonstrates the great potential for the direct-synthesis protocol of PbS CQDs.
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http://dx.doi.org/10.1002/adma.202207293 | DOI Listing |
Phys Chem Chem Phys
December 2024
School of Physical and Chemical Sciences, Queen Mary University of London, Mile End Road, London E1 4NS, UK.
Molten salts are important in a number of energy applications, but the fundamental mechanisms operating in ionic liquids are poorly understood, particularly at higher temperatures. This is despite their candidacy for deployment in solar cells, next-generation nuclear reactors, and nuclear pyroprocessing. We perform extensive molecular dynamics simulations over a variety of molten chloride salt compositions at varying temperature and pressures to calculate the thermodynamic and transport properties of these liquids.
View Article and Find Full Text PDFSmall
December 2024
Institute of Polymer Optoelectronic Materials & Devices, Guangdong Basic Research Center of Excellence for Energy & Information Polymer Materials, State Key Laboratory of Luminescent Materials & Devices, South China University of Technology, Guangzhou, 510640, China.
Polymer hole transport materials offer significant efficiency and stability advantages for p-i-n perovskite solar cells. However, the energetic disorder of amorphous polymer hole transport materials not only limits carrier transport but also impedes contact between the polymer and perovskite, hindering the formation of high crystalline quality perovskites. Herein, a novel low energetic disordered polymer hole transport material, PF8ICz, featuring an indeno[3,2-b]carbazole unit with extended π-conjugation is designed and synthesized.
View Article and Find Full Text PDFSmall Methods
December 2024
Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201, China.
The development of front-side pastes suitable for devices with high sheet resistance such as tunnel oxide passivated contact (TOPCon), is of great significance but remains a considerable challenge. The optimization of the Ag-Si contact interface is crucial for enhancing contact and improving the efficiency of these devices. This work investigates the front-side Ag pastes with low Al content (<2 wt.
View Article and Find Full Text PDFWe report Er emission in YAlO host, sensitized by Cr. The excitation bands of Cr at 416 and 555 nm are broad and effectively cover the region 400-600 nm. The phosphor can be useful for converting 400-600 nm radiations to infrared (IR) light around 1521 nm.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing 400714, China. Electronic address:
Hydrogen is increasingly acknowledged as a viable alternative to traditional fossil fuels. However, the photothermal properties of CoFeS, a photocatalyst displaying metal-like behavior, have not been adequately explored in the context of photocatalytic H generation. To improve photocatalytic hydrogen evolution, it is crucial to understand how to expedite the transfer of photogenerated electrons and the dissociation of H-OH bonds for enhanced hydrogen ion release.
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