Publications by authors named "Li-Chyong Chen"

2D MoS holds great promise for spintronics, yet is limited by intrinsic diamagnetism. This study demonstrates inducing ferromagnetic behavior in MoS films doped with 0.47% Gd, achieving an ultrahigh saturation magnetization of 454 emu/cm in a few-layered film over 11-times higher than bulk films (40 nm).

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In situ mapping of interfacial electron transfer dynamics to reveal electrocatalytic activity with high spatial resolution is crucial for developing efficient electrochemical devices. While emerging 2D materials for catalysis have attracted substantial attention, there is still a notable lack of studies examining their electrochemical properties at the nanoscale, particularly in a layer-by-layer context. Here, both outer-sphere and inner-sphere electron transfer at a 2D semiconducting WSe electrode-electrolyte interface are spatially resolved and quantified in high resolution.

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The narrow bandgap InN material, with exceptional physical properties, has recently gained considerable attention, encouraging many scientists/engineers to design infrared photodetectors, light-emitting diodes, laser diodes, solar cells, and high-power electronic devices. The InN/Sapphire samples of different film thicknesses that we have used in our methodical experimental and theoretical studies are grown by plasma-assisted molecular-beam epitaxy. Hall effect measurements on these samples have revealed high-electron-charge carrier concentration, η.

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The traditional sulfur selenization process in CuZnSn(S,Se) (CZTSSe) solar cell fabrication often results in the creation of localized anion vacancies ( and ). These vacancies are considered harmful defects as they can trap carriers generated by light, leading to reduced solar cell efficiency. Moreover, concrete evidence has been lacking on the extent of the impact caused by these anion vacancies.

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Black GaAs nanotip arrays (NTs) with 3300 nm lengths were fabricated via self-masked plasma etching. We show, both experimentally and numerically, that these NTs, with three gradient refractive index layers, effectively suppress Fresnel reflections at the air-GaAs interface over a broad range of wavelengths. These NTs exhibit exceptional UV-Vis light absorption (up to 99%) and maintain high NIR absorption (33-60%) compared to bare GaAs.

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Article Synopsis
  • The study addresses challenges in photocatalytic CO reduction reactions, specifically the need for intrinsic active sites and the fast recombination of charge carriers.
  • Researchers developed a novel phosphorus and boron binary-doped graphitic carbon nitride material, which shows significantly enhanced photocatalytic activity for selective CO generation due to its unique structural properties.
  • The combination of dual dopants and porous structure activates specific nitrogen atoms, stabilizes reaction intermediates, and enhances light absorption, leading to a CO yield that is approximately 12 times greater than traditional graphitic carbon nitride.
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An electrochemical capacitor configuration extends its operational potential window by leveraging diverse charge storage mechanisms on the positive and negative electrodes. Beyond harnessing capacitive, pseudocapacitive, or Faradaic energy storage mechanisms and enhancing electrochemical performance at high rates, achieving a balance of stored charge across electrodes poses a significant challenge over a wide range of charge-discharge currents or sweep rates. Consequently, fabricating hybrid and asymmetric supercapacitors demands precise electrochemical evaluations of electrode materials and the development of a reliable methodology.

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Metal-semiconductor nanocomposites have emerged as a viable strategy for concurrently tailoring both thermal and electronic transport properties of established thermoelectric materials, ultimately achieving synergistic performance. In this investigation, a series of nanocomposite thin films were synthesized, embedding metallic cobalt telluride (CoTe) nanophase within the nanocrystalline ternary skutterudite (Co(GeSb)Te or CGST) matrix. Our approach harnessed composition fluctuation-induced phase separation and in situ growth during thermal annealing to seamlessly integrate the metallic phase.

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Double-atom site catalysts (DASs) have emerged as a recent trend in the oxygen reduction reaction (ORR), thereby modifying the intermediate adsorption energies and increasing the activity. However, the lack of an efficient dual atom site to improve activity and durability has limited these catalysts from widespread application. Herein, the nitrogen-coordinated iron and tin-based DASs (Fe-Sn-N/C) catalyst are synthesized for ORR.

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Article Synopsis
  • Designing efficient organic polymer photocatalysts for hydrogen production using visible and near-infrared (NIR) light remains challenging.
  • Researchers developed a new series of polymer nanoparticles (Pdots) using ITIC and BTIC units with different π-linkers, which work effectively alone without needing to combine with other materials.
  • The difluorothiophene (ThF) π-linker improves charge transfer between donor and acceptor components in the polymers, resulting in significantly enhanced hydrogen production rates of 279 µmol/h with visible light and 20.5 µmol/h with NIR light, and an apparent quantum yield of 4.76% at 700 nm.
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Atomically dispersed iron sites on nitrogen-doped carbon (Fe-NC) are the most active Pt-group-metal-free catalysts for oxygen reduction reaction (ORR). However, due to oxidative corrosion and the Fenton reaction, Fe-NC catalysts are insufficiently active and stable. Herein, w e demonstrated that the axial Cl-modified Fe-NC (Cl-Fe-NC) electrocatalyst is active and stable for the ORR in acidic conditions with high H O tolerance.

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Article Synopsis
  • The electrochemical reduction of oxygen into hydrogen peroxide (H2O2) in acidic conditions is a greener, energy-efficient alternative to the traditional anthraquinone process but faces challenges like high overpotential and low production rates.
  • A new approach mimics a metalloenzyme-like structure using carbon-based single-atom electrocatalysts, specifically CoNOC, which shows over 98% selectivity for H2O2 production in an acidic medium.
  • The study employs X-ray absorption spectroscopy and density functional theory calculations to analyze the optimal structural characteristics of the CoNOC active site, achieving high selectivity and mass activity for H2O2 synthesis.
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GaN nanowires (NWs) grown on silicon via atmospheric pressure chemical vapor deposition were doped with Cobalt (Co) by ion implantation, with a high dose concentration of 4 × 10 cm, corresponding to an average atomic percentage of ~3.85%, and annealed after the implantation. Co-doped GaN showed optimum structural properties when annealed at 700 °C for 6 min in NH ambience.

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The widespread use of energy storage technologies has created a high demand for the development of novel anode materials in Li-ion batteries (LIBs) with high areal capacity and faster electron-transfer kinetics. In this work, carbon-coated CuZnSnS with a hierarchical 3D structure (CZTS@C) is used as an anode material for LIBs. The CZTS@C microstructures with enhanced electrical conductivity and improved Li-ion diffusivity exhibit high areal and gravimetric capacities of 2.

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Article Synopsis
  • The study focuses on understanding how defects and edge atoms in monolayer 2H-WSe materials can improve the efficiency of photocatalysts for CO reduction to CH.* -
  • Findings show that edge atoms facilitate better CO binding and lead to higher solar-to-fuel quantum efficiency, especially influenced by the size of the material flakes.* -
  • Nanoscale mapping reveals that edges are the optimal sites for electron transfer, suggesting potential for new monolayer materials as low-cost co-catalysts in energy conversion processes.*
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We report the phase evolution and thermoelectric properties of a series of Co(GeTe)Sb ( = 0-0.20) compositions synthesized by mechanical alloying. Pristine ternary Co(GeTe) skutterudite crystallizes in the rhombohedral symmetry (3̅), and Sb doping induces a structural transition to the cubic phase (ideal skutterudite, 3̅).

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Effects of electronic and atomic structures of V-doped 2D layered SnS are studied using X-ray spectroscopy for the development of photocatalytic/photovoltaic applications. Extended X-ray absorption fine structure measurements at V K-edge reveal the presence of VO and VS bonds which form the intercalation of tetrahedral OVS sites in the van der Waals (vdW) gap of SnS layers. X-ray absorption near-edge structure (XANES) reveals not only valence state of V dopant in SnS is ≈4 but also the charge transfer (CT) from V to ligands, supported by V L resonant inelastic X-ray scattering.

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A heterobimetallic corrole complex, comprising oxygen reduction reaction (ORR) active non-precious metals Co and Fe with a corrole-N4 center (PhFCC), is successfully synthesized and used to prepare a dual-atom molecular catalyst (DAMC) through subsequent low-temperature pyrolysis. This low-temperature pyrolyzed electrocatalyst exhibited impressive ORR performance, with onset potentials of 0.86 and 0.

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  • The report examines the use of Ag/g-CN/ZnO nanorods for effectively removing pharmaceutical drugs from wastewater through a photocatalytic oxidation process, highlighting its environmentally friendly nature.
  • These catalysts are created using simple, eco-friendly methods, with g-CN/ZnO nanorods formed via self-assembly and Ag nanoparticles added through photoreduction.
  • Results reveal that these nanorods can significantly degrade common drugs like paracetamol, amoxicillin, and cefalexin at high concentrations, outperforming traditional catalysts and demonstrating strong reusability and stability over multiple cycles of use.
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  • This study showcases the innovative use of a hybrid photocatalyst combining poly(3-hexylthiophene-2,5-diyl) (P3HT) nanoparticles and graphene oxide (GO) to efficiently convert CO into useful hydrocarbons with high selective production, specifically methanol and acetaldehyde.
  • The hybrid photocatalyst achieves a solar-to-fuel conversion efficiency 13.5 times greater than pure GO, thanks to P3HT's role in enhancing light absorption and facilitating charge transfer within the system.
  • Advanced fluorescence techniques revealed that improved interfacial manipulation leads to quicker charge transfer from P3HT to GO, making this metal-free, non-toxic, and low-cost catalyst a promising solution for CO reduction into solar
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Layered MoS is considered as one of the most promising two-dimensional photocatalytic materials for hydrogen evolution and water splitting; however, the electronic structure at the MoS-liquid interface is so far insufficiently resolved. Measuring and understanding the band offset at the surfaces of MoS are crucial for understanding catalytic reactions and to achieve further improvements in performance. Herein, the heterogeneous charge transfer behavior of MoS flakes of various layer numbers and sizes is addressed with high spatial resolution in organic solutions using the ferrocene/ferrocenium (Fc/Fc) redox pair as a probe in near-field scanning electrochemical microscopy, i.

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Recent advances in nanotechnology, especially the development of integrated nanostructured materials, have offered unprecedented opportunities for photocatalytic CO2 reduction. Compared to bulk semiconductor photocatalysts, most of these nanostructured photocatalysts offer at least one advantage in areas such as photogenerated carrier kinetics, light absorption, and active surface area, supporting improved photochemical reaction efficiencies. In this review, we briefly cover the cutting-edge research activities in the area of integrated nanostructured catalysts for photochemical CO2 reduction, including aqueous and gas-phase reactions.

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Nonnoble metal catalysts are low-cost alternatives to Pt for the oxygen reduction reactions (ORRs), which have been studied for various applications in electrocatalytic systems. Among them, transition metal complexes, characterized by a redox-active single-metal-atom with biomimetic ligands, such as pyrolyzed cobalt-nitrogen-carbon (Co-N/C), have attracted considerable attention. Therefore, we reported the ORR mechanism of pyrolyzed Vitamin B12 using operando X-ray absorption spectroscopy coupled with electrochemical impedance spectroscopy, which enables operando monitoring of the oxygen binding site on the metal center.

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Most chemical vapor deposition methods for transition metal dichalcogenides use an extremely small amount of precursor to render large single-crystal flakes, which usually causes low coverage of the materials on the substrate. In this study, a self-capping vapor-liquid-solid reaction is proposed to fabricate large-grain, continuous MoS films. An intermediate liquid phase-NaMoO is formed through a eutectic reaction of MoO and NaF, followed by being sulfurized into MoS.

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