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.

EO polymer at cryogenic temperatures

Abstract: Electro-optic (EO) properties at 7 K of a guest–host type nonlinear poled polymer system consisting of AJLZ53 chromophores in an amorphous polycarbonate host are reported for the first time. A modified attenuated total reflection method that takes into account multilayer structure is used to accurately characterise linear and nonlinear optical properties. At the telecommunication wavelength of 1550 nm, <10% drop of the EO coefficient r 33 at 7 K is observed compared with that at 300 K, while n 3 r 33 only decreases <5% because of increased anisotropic indices of refraction at low temperatures. This decrease of the r 33 at 7 K indicates that the EO activity of nonlinear polymers at room temperatures is not of pure electronic origin because of vibrational mode contributions to the first-order hyperpolarisability.

Nonlinear refraction and absorption measurements of thin films by the dual-arm Z-scan method.

Abstract: We extend the recently developed dual-arm Z-scan to increase the signal-to-noise ratio (SNR) for measuring the nonlinear refraction (NLR) of thin films on thick substrates. Similar to the case of solutes in solution, the phase shift due to NLR in a thin film can often be dominated by the phase shift due to NLR in the much thicker substrate. SNR enhancement is accomplished by simultaneously scanning a bare substrate and the film plus substrate in two separate but identical Z-scan arms. The subtraction of these signals taken simultaneously effectively cancels the nonlinear signal from the substrate, leaving only the signal from the film. More importantly, the SNR is increased since the correlated noise from effects such as beam-pointing instabilities cancels. To show the versatility of the dual-arm Z-scan method, we perform measurements on semiconductor and organic thin films, some less than 100 nm thick and with thicknesses up to 4 orders of magnitude less than the substrate.

Possible interfacial ion/charge accumulation in thin-film perovskite/fullerene surfactant planar heterojunction solar cells

Abstract: Organic–inorganic hybrid perovskite solar cells (PVSCs) have become the most promising photovoltaic technology nowadays, considering its low-cost and low-temperature manufacturing processes and superior power conversion efficiency In addition to efficiency optimization, understanding the fundamental properties of the perovskite materials and the related device physics, such as hysteresis and stability, has also attracted significant research interest In this study, we manifested the fact that the hysteretic behavior of PVSC is strongly correlated with the structure design of the adjacent charge-transporting layer (CTL) The constituent ions in CTL are very likely to induce severe device hysteresis based on the analyses from the capacitance-voltage and electrochemical impedance spectroscopy By further applying Warburg impedance to simulate the impedance spectrum at the low-frequency region, distinct kinetics of ion movement at different perovskite/electron-transporting layer interfaces are clearly revealed This work unveils the close interactions between the perovskite material and the ions from adjacent CTLs, providing a new perspective on the future molecular design of CTLs for PVSCs

Progress on heteroaromatic chromophores in high-temperature polymers for electro-optic applications

Abstract: We have developed several classes of thermally stable nonlinear optical chromophores based on the combination of efficient thiophene conjugating units and novel electron-donating and electron-accepting functional groups. The incorporation of these chromophores into high temperature polymers produces high linear electro-optic coefficients and long-term thermal stability at elevated temperatures. Active Mach-Zehnder interferometers with a V(pi) phase shift of 50 volts and low attenuation (< 2 dB/cm) were fabricated. Thermal baking of the poled device demonstrated no change in activity after 30 minutes at 230 degree(s)C.

Two-Photon Lithography of Platinum-Porphyrin Oxygen Sensors

Abstract: Oxygen sensing structures were generated by two-photon microfabrication. By copolymerizing metalloporphyrins with a two-photon (2P) photo-initiated polymer, oxygen sensors were patterned into complex 3-D shapes. The sensors were generated on the interior walls of small bore capillaries to allow for controlled concentrations of oxygenated water and cell-rich media to be pumped through their local environment. Phosphorescence lifetime of the patterns were acquired at known levels of O2 as a standard for measuring the respiration rate of a tiny population of bacterial cells. In addition, we report that the inclusion of the Pt-Porphyrin significantly reduces the 2P polymerization threshold. Fabricating near the inferred polymerization threshold, 3-D structures as small as 50 nm were observed in both the Pt-Porphyrin enhanced and the pure photopolymerizable monomers

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%.