Author
Alex K.-Y. Jen
Other affiliations: University of Nebraska–Lincoln, Zhejiang California International NanoSystems Institute, University of Washington ...read more
Bio: Alex K.-Y. Jen is an academic researcher from City University of Hong Kong. The author has contributed to research in topics: Perovskite (structure) & Polymer solar cell. The author has an hindex of 128, co-authored 921 publications receiving 61811 citations. Previous affiliations of Alex K.-Y. Jen include University of Nebraska–Lincoln & Zhejiang California International NanoSystems Institute.
Papers published on a yearly basis
Papers
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TL;DR: In this article, the power conversion efficiency of poly(indacenodithiophene-co-phananthrene-quinoxaline) (PIDT-PhanQ)/[6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) based bulk- heterojunction (BHJ) solar cells was achieved upon adding tetrahydrofuran (THF) as a co-solvent to 1,2-dichlorobenzene (DCB).
Abstract: Improved power conversion efficiency of poly(indacenodithiophene-co-phananthrene-quinoxaline) (PIDT-PhanQ)/[6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) based bulk- heterojunction (BHJ) solar cells was achieved upon adding tetrahydrofuran (THF) as a co-solvent to 1,2-dichlorobenzene (DCB). This reasonably large enhancement is achieved due to THF changes the morphology in the active layer by reducing the solvent-solute interaction. The Flory-Huggins interaction parameter and cohesive energy densities for PIDT-PhanQ and PD71BM with different solvents were further studied to understand the underlying phase separation mechanism in BHJ films.
10 citations
TL;DR: In this article, a new approach to polymer cross-linking was investigated using a cascading cycloreversion of a maleimide-furan adduct and a double 1,3-dipolar cycloaddition between a sydnone and maleimides.
Abstract: A new approach to polymer cross-linking is investigated using a cascading cycloreversion of a maleimide-furan adduct and a double 1,3-dipolar cycloaddition between a sydnone and maleimide. The cross-linking proceeds quantitatively above 63 °C, despite the polymer possessing no observable glass transition temperature. The resulting polymer network possesses a high thermal stability (>300 °C) due to the irreversibility of the sydnone-maleimide cycloaddition, which releases CO2 during the cross-linking, driving the reaction. The rigid three-dimensional structure of the bis-maleimide-sydnone cycloadduct produced local free volumes in films, decreasing the dielectric constant of the material.
10 citations
TL;DR: In this article, a three-layered slab waveguide with metal-slotted optical waveguides (MSOWs) using an electro-optic polymer material has been experimentally demonstrated.
Abstract: Metal-slotted optical waveguides (MSOWs) using an electro-optic polymer material have been experimentally demonstrated. The device consists of a three-layered slab waveguide in that the thin metal (gold) film strips are embedded on top of the lower cladding. The optical mode shapes and effective index of the propagation modes of the proposed waveguide structure were calculated using a simplified effective index method and a simulation tool. The fabrication and the device characteristics of a variable optical attenuator and an optical phase modulator based on MSOWs are discussed.
10 citations
Patent•
28 Oct 2009
TL;DR: In this article, a chamber device for analyzing living cell(s) is presented. Butts et al. use a base and a lid that when reversibly pressed closed create a chamber.
Abstract: A chamber device for analyzing living cell(s). The chamber device includes a base and a lid that when reversibly pressed closed create a chamber. The base is configured with an optically transparent well to contain at least one cell. The lid has a breadth greater than the base and is configured to contain at least one sensor. The lid is further configured with a lip that when pressed between the lid and the base creates an impermeable seal. The base and the lid are configured so that, when closed and in use, the sensor remains spatially apart from the at least one cell.
10 citations
TL;DR: In this article, the state-of-the-art solution-processed perovskite solar cells have reached the compelling power conversion efficiency (PCE) of 22.1%, comparable with most of the current single-junction nonconcentrated commercialized solar cells.
Abstract: The state-of-the-art solution-processed perovskite solar cells (PVSCs) have reached the compelling power conversion efficiency (PCE) of 22.1%, comparable with most of the current single-junction nonconcentrated commercialized solar cells. However, the development of scalable printing and coating techniques compatible with the fabrication of PVSCs in ambient conditions still lags behind, due to the following two reasons: 1) The ambient oxygen and moisture significantly degrade the characteristics and functionality of the perovskite films, and 2) most of the research groups focus on the lab-scale spin-coating, hindering gaining knowledge and experience required to understand and employ scalable methods. In this paper, we fabricated all layers of the PVSCs, except for the back contact, by scalable blade-coating method, performed in ambient conditions, and achieved a high PCE of 11.1%, with superior device stability. Through selecting a nonhalide source and strong reducing agent, we alleviated the oxidation problem in ambient conditions. Moreover, we found an optimized blade-coater substrate temperature of 125 °C, which can yield micrometer-scale perovskite domain size created by thermocapillary Marangoni motion, high crystallinity, large absorption, and prolonged carrier lifetime. These results are promising for manufacturing PVSCs in high volume and in ambient conditions.
10 citations
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TL;DR: In this article, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
Abstract: Organic-inorganic perovskites have shown promise as high-performance absorbers in solar cells, first as a coating on a mesoporous metal oxide scaffold and more recently as a solid layer in planar heterojunction architectures. Here, we report transient absorption and photoluminescence-quenching measurements to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide (CH3NH3PbI(3-x)Cl(x)) and triiodide (CH3NH3PbI3) perovskite absorbers. We found that the diffusion lengths are greater than 1 micrometer in the mixed halide perovskite, which is an order of magnitude greater than the absorption depth. In contrast, the triiodide absorber has electron-hole diffusion lengths of ~100 nanometers. These results justify the high efficiency of planar heterojunction perovskite solar cells and identify a critical parameter to optimize for future perovskite absorber development.
8,199 citations
Journal Article•
TL;DR: In this paper, transient absorption and photoluminescence-quenching measurements were performed to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide and triiodide perovskite absorbers.
Abstract: Organic-inorganic perovskites have shown promise as high-performance absorbers in solar cells, first as a coating on a mesoporous metal oxide scaffold and more recently as a solid layer in planar heterojunction architectures. Here, we report transient absorption and photoluminescence-quenching measurements to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide (CH3NH3PbI(3-x)Cl(x)) and triiodide (CH3NH3PbI3) perovskite absorbers. We found that the diffusion lengths are greater than 1 micrometer in the mixed halide perovskite, which is an order of magnitude greater than the absorption depth. In contrast, the triiodide absorber has electron-hole diffusion lengths of ~100 nanometers. These results justify the high efficiency of planar heterojunction perovskite solar cells and identify a critical parameter to optimize for future perovskite absorber development.
6,454 citations
TL;DR: Perovskite films received a boost in photovoltaic efficiency through controlled formation of charge-generating films and improved current transfer to the electrodes and low-temperature processing steps allowed the use of materials that draw current out of the perovskites layer more efficiently.
Abstract: Advancing perovskite solar cell technologies toward their theoretical power conversion efficiency (PCE) requires delicate control over the carrier dynamics throughout the entire device. By controlling the formation of the perovskite layer and careful choices of other materials, we suppressed carrier recombination in the absorber, facilitated carrier injection into the carrier transport layers, and maintained good carrier extraction at the electrodes. When measured via reverse bias scan, cell PCE is typically boosted to 16.6% on average, with the highest efficiency of ~19.3% in a planar geometry without antireflective coating. The fabrication of our perovskite solar cells was conducted in air and from solution at low temperatures, which should simplify manufacturing of large-area perovskite devices that are inexpensive and perform at high levels.
5,789 citations
TL;DR: This paper presents a meta-analysis of the chiral stationary phase transition of Na6(CO3)(SO4)2, a major component of the response of the immune system to Na2CO3.
Abstract: Ju Mei,†,‡,∥ Nelson L. C. Leung,†,‡,∥ Ryan T. K. Kwok,†,‡ Jacky W. Y. Lam,†,‡ and Ben Zhong Tang*,†,‡,§ †HKUST-Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen 518057, China ‡Department of Chemistry, HKUST Jockey Club Institute for Advanced Study, Institute of Molecular Functional Materials, Division of Biomedical Engineering, State Key Laboratory of Molecular Neuroscience, Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China Guangdong Innovative Research Team, SCUT-HKUST Joint Research Laboratory, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China
5,658 citations
TL;DR: An approach for depositing high-quality FAPbI3 films, involving FAP bI3 crystallization by the direct intramolecular exchange of dimethylsulfoxide (DMSO) molecules intercalated in PbI2 with formamidinium iodide is reported.
Abstract: The band gap of formamidinium lead iodide (FAPbI3) perovskites allows broader absorption of the solar spectrum relative to conventional methylammonium lead iodide (MAPbI3). Because the optoelectronic properties of perovskite films are closely related to film quality, deposition of dense and uniform films is crucial for fabricating high-performance perovskite solar cells (PSCs). We report an approach for depositing high-quality FAPbI3 films, involving FAPbI3 crystallization by the direct intramolecular exchange of dimethylsulfoxide (DMSO) molecules intercalated in PbI2 with formamidinium iodide. This process produces FAPbI3 films with (111)-preferred crystallographic orientation, large-grained dense microstructures, and flat surfaces without residual PbI2. Using films prepared by this technique, we fabricated FAPbI3-based PSCs with maximum power conversion efficiency greater than 20%.
5,458 citations