Alex K.-Y. Jen

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.

All-organic and organic-silicon photonic ring micro-resonators

Abstract: Organic electro-optic materials offer exceptional processability (both from solution and the gas phase) that permit fabrication of flexible and conformal device structures and the integration of organic materials with a wide range of disparate materials. In addition, organic electro-optical materials have fundamental response times that are in the terahertz region, and useable electro-optic coefficients that are approaching 300 pm/V (at telecommunication wavelengths). In addition to fabrication by traditional lithographic methods, multiple devices on a single wafer have been fabricated by soft and nano-imprint lithography. In this presentation, we review the fabrication and performance evaluation of a number of all-organic and organic-silicon photonic ring microresonator devices. Both electrical and thermal tuning of devices, including both single and multiple ring micro-resonators, are demonstrated.

A Living Cell Array (LCA) for Multiparameter Cell Metabolism Studies

Abstract: A proof-of-platform-concept architecture for the analysis of living cell arrays is presented. Initial experiments conducted show a conceptual design for single-cell multiparameter measurements in real time. As a first parameter, extensive development and experimentation have been conducted on a sensor that will measure single-cell oxygen consumption. Wafer-level processing for chip fabrication and sensor deposition has been achieved, making possible the future goal of an automated system using disposable chips. The oxygen sensor has been tested for long-term adherence to a substrate in aqueous environments, biocompatibility with cell types of interest, and sensitivity to small changes in local oxygen concentration. A test device was made to verify the use of a gold foil barrier as an oxygen seal and shows good isolation of sealed areas

Low-voltage electro-optic polymer modulators

Abstract: Electro-optic (EO) polymer modulators have demonstrated high speed external modulation of optical signals. Additionally, EO polymers have closely matched refractive indices at optical and microwave wavelengths, which enables high bandwidth operation. An EO polymer includes a polymer matrix and an organic "push-pull" chromophore that can be modified to give poled polymers with high EO activity. This high EO activity and optical-microwave velocity match offer the promise of accomplishing broadband, high speed optical modulation with low drive voltage. Such optical signal modulation is critical for applications in phased array radar and RF photonics. However, practical fabrication of optical modulators that realize the potential of EO polymers requires clad materials with optimized properties such as conductivity, dielectric constant, optical loss, and refractive index. In addition, other practical issues such as electrode design, optical fiber coupling, and hermetic packaging are critical in final device performance. We report on high-speed electrode parameters as well as electro-optic performance versus frequency of modulators fabricated on 6" silicon wafers. The r33 values measured on single layer thin films are compared with those resulting from Vπ measurements on devices. We compare the effect of EO polymer morphology on device fabrication and optical loss for different EO polymers.© (2006) COPYRIGHT SPIE--The International Society for Optical Engineering. Downloading of the abstract is permitted for personal use only.

Electro-optic polymer prism beam deflector

Abstract: We report on an optical beam deflector capable of achieving a large beam deflection using a planar thermoplastic-based electro-optic (EO) polymer prism. By optimizing the prism's geometry, relative position, and incident angle of the input beam, the device shows that a large deflection angle can be achieved through a relatively small index change from a single EO polymer prism stage. In this paper, we present the design and fabrication of the deflector using a simple hot-embossing technique. Beam deflection experiments were conducted, and a maximum deflection angle of 5.6 deg was observed, in agreement with our predicted value.

Spontaneously poling of electro-optic polymer thin films across a 1.1-mm thick glass substrate by pyroelectric crystals

Abstract: We developed a method to pole electro-optic (E-O) polymer thin films using pyroelectric crystals instead of external high voltage source unit. The process is based on a multi-layered dielectric stack, in which micron-thick E-O polymer films were sandwiched between millimeter thick pyroelectric crystal and borosilicate glass substrate. Through modest temperature change, very large electric fields could be spontaneously generated from pyroelectric effect of the crystals, which can deliver high effective field strength (up to 0.7 MV/cm) to the E-O polymer thin films across the glass plate. Very intriguing phenomena of significantly reduced leak through current (LTC) and improved dielectric breakdown strength of E-O polymers were observed. As a result, large Pockels coefficients of 62 pm/V at 1.31 μm can be obtained for poled E-O thin films. The good agreement between theory and experimentally measured results in the study provide important insights of electrostatics in pyroelectric systems and their effectiv...

Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

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.

Electron-Hole Diffusion Lengths Exceeding 1 Micrometer in an Organometal Trihalide Perovskite Absorber

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.

Interface engineering of highly efficient perovskite solar cells

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.

Aggregation-Induced Emission: Together We Shine, United We Soar!

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

High-performance photovoltaic perovskite layers fabricated through intramolecular exchange

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%.