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1. Improving PbS Colloidal Quantum Dot Solar Cell Performance via Solution-Phase Engineering

   https://doi.org/10.1109/PVSC48320.2023.10359532  

   Gudi, Dhanvini; Chiu, Arlene; Kachman, Dana; Rong, Eric; Kamal, Serene; Lan, Yucheng; Thon, Susanna M (June 2023, IEEE)

   Lead Sulfide (PbS) colloidal quantum dots (CQDs) are promising materials for flexible and wearable photovoltaic devices and technologies due to their low cost, solution processibility and bandgap tunability with quantum dot size. However, PbS CQD solar cells have limitations on performance efficiency due to charge transport losses in the CQD layers and hole transport layer (HTL). This study pursues two promising techniques in parallel to address these challenges. Solution-phase annealing of the absorbing PbS-PbX2 (X = Br, I) layer can reduce charge transport losses by removing oleic acid and parasitic hydroxyl ligands. Additionally, optoelectronic simulations are used to show that HTL performance can be improved by the addition of a 2D transition metal dichalcogenide (TMD) layer to the PbS CQD-based HTL. We use solution-phase exfoliation to produce and incorporate 2D WSe2 nanoflakes into the HTL. We report a power conversion efficiency (PCE) increase of up to 3.4% for the solution-phase-annealed devices and up to 1% for the 2D WSe2 HTL augmented devices. A combination of these two techniques should result in high-performing PbS CQD solar cells, paving the way for further advancements in flexible photovoltaics. 

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2. Simultaneous Enhancement of Efficiency and Operational‐Stability of Mesoscopic Perovskite Solar Cells via Interfacial Toughening

   https://doi.org/10.1002/adma.202308819  

   Yang, In Seok; Dai, Zhenghong; Ranka, Anush; Chen, Du; Zhu, Kai; Berry, Joseph J.; Guo, Peijun; Padture, Nitin P. (May 2024, Advanced Materials)

   The combined effects of compact TiO2 (c-TiO2) electron-transport layer (ETL) are investigated without and with mesoscopic TiO2 (m-TiO2) on top, and without and with an iodine-terminated silane self-assembled monolayer (SAM), on the mechanical behavior, opto–electronic properties, photovoltaic (PV) performance, and operational-stability of solar cells based on metal-halide perovskites (MHPs). The interfacial toughness increases almost threefold in going from c-TiO2 without SAM to m-TiO2 with SAM. This is attributed to the synergistic effect of the m-TiO2/MHP nanocomposite at the interface and the enhanced adhesion afforded by the iodine-terminated silane SAM. The combination of m-TiO2 and SAM also offers a significant beneficial effect on the photocarriers extraction at the ETL/MHP interface, resulting in perovskite solar cells (PSCs) with power-conversion efficiency (PCE) of over 24% and 20% for 0.1 and 1 cm2 active areas, respectively. These PSCs also have exceptionally long operational-stability lives: extrapolated T80 (duration at 80% initial PCE retained) is ≈18 000 and 10 000 h for 0.1 and 1 cm2 active areas, respectively. Postmortem characterization and analyses of the operational-stability-tested PSCs are performed to elucidate the possible mechanisms responsible for the long operational-stability. 

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3. Spectrally-selective Photovoltaics via Photonic Band Engineering in Absorbing Media

   https://doi.org/10.1109/PVSC40753.2019.8980467  

   Chiu, Arlene; Qiu, Botong; Lin, Yida; Arinze, Ebuka S.; Li, Lulin; Thon, Susanna M. (June 2019, Spectrally-selective Photovoltaics via Photonic Band Engineering in Absorbing Media)

   Spectral selectivity is of interest for many photovoltaic applications, such as in multijunction and transparent solar cells, where wavelength-selectivity of the photoactive material is necessary. We investigate using artificial photonic band engineering as a method for achieving spectral selectivity in an absorbing material such as PbS CQD thin films. Using FDTD simulations, we find that a CQD-based photonic crystal (CQD-PC) is able to maintain its photonic band structure, including the existence of a reduced photonic density of states, in the presence of weak material absorption. This shows that CQD-PCs are a promising material for photovoltaic applications that require spectral selectivity. 

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4. 4-T CdTe/Perovskite Thin Film Tandem Solar Cells with Efficiency >24%

   https://doi.org/10.1021/acsenergylett.4c01118  

   Paul, Ananta; Singha, Abhijit; Hossain, Kashimul; Gupta, Saurabh; Misra, Manas; Mallick, Sudhanshu; Munshi, Amit H; Kabra, Dinesh (May 2024, ACS Energy Letters)

   De_Angelis, Filippo (Ed.)

   An integration of perovskite and cadmium telluride (CdTe) solar cells in a tandem configuration has the potential to yield efficient thin-film tandem solar cells. Owing to the promise of higher efficiency at low cost, the presented study aims to explore the potential for combining this commercially established CdTe photovoltaics (PV) with next-generation perovskite PV. Here, we developed four-terminal (4-T) CdTe/perovskite tandem solar cells, starting with 18.3% efficient near-infrared-transparent perovskite solar cells (NIR-TPSCs) with an average transmission (Tavg) of 24.76% in the 300−900 nm wavelength range. These were then integrated with 19.56% efficient opaque CdTe solar cells, achieving 23.42% efficiency in a 4-T tandem configuration. Additionally, using a refractive index matching liquid increases the overall power conversion efficiency (PCE)to 24.2%. This pioneering achievement marks the first instance of a 4-T CdTe/perovskite thin-film tandem solar cell exceeding a PCE of 24.2%, a significant 123.72% increase in overall PCE. 

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5. Effect of ligand groups on photoexcited charge carrier dynamics at the perovskite/TiO ₂ interface

   https://doi.org/10.1039/d1ra05306j  

   Johnson, Landon; Kilin, Dmitri (December 2021, RSC Advances)

   The work proposed here aims to describe the dynamics of photoexcited charge carriers at the interface between the perovskite and electron transport layer (ETL) in perovskite solar cells (PSCs) and the effect that the interface morphology has on these dynamics. This is done in an effort to further develop the understanding of these materials so that their chemical composition and morphology may be better utilized to improve PSCs by means of increasing the power conversion efficiency (PCE), maximizing the chemical stability of PSCs to lengthen their lifespan, finding the cheapest and easiest materials to synthesize which have beneficial properties in photovoltaics, etc. This is done by using density functional theory to model the interface and open system Redfield theory to describe the charge carrier dynamics. We find that the charge transfer characteristics at the perovskite/ETL interface depend greatly on the choice of ligands adsorbed on the ETL that act as a bridge between the perovskite and ETL. The two ligand choices discussed here go so far as to determine whether the system will undergo a Förster energy transfer or a Dexter energy transfer upon photoexcitation. 

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