Alexander K. Ng

Bio: Alexander K. Ng is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Nanoporous & Materials science. The author has an hindex of 1, co-authored 3 publications receiving 27 citations. Previous affiliations of Alexander K. Ng include St. John's University.

Hierarchical Bulk Nanoporous Aluminum for On-Site Generation of Hydrogen by Hydrolysis in Pure Water and Combustion of Solid Fuels

Abstract: There are still many scientific and engineering challenges that need to be addressed before a true sustainable hydrogen economy can be realized. Three of these challenges include sustainable hydrog...

Eco-friendly Synthesis of Nanoporous Magnesium by Air-Free Electrolytic Dealloying with Recovery of Sacrificial Elements for Energy Conversion and Storage Applications

Abstract: The synthesis of nanoporous Mg with minimal surface oxide coverage has been hindered by its high chemical reactivity. Herein, we demonstrate the fabrication of three-dimensional bicontinuous nanoporous Mg with ligament and pore sizes in the range of 20–30 nm using air-free electrolytic dealloying with recovery of the sacrificial material. The starting material consists of a magnesium–lithium parent alloy with lithium as the sacrificial component. During selective electrolytic leaching in an anhydrous lithium-conducting organic electrolyte solvent, the sacrificial lithium is stripped from the magnesium–lithium parent alloy used as the working electrode and plated on a pure lithium foil used as the counter electrode, enabling sacrificial element recovery, making the process eco-friendly. The morphology of the fabricated nanoporous Mg was thoroughly investigated using electron microscopy techniques, inductively coupled plasma (ICP) spectroscopy, X-ray photoelectron spectroscopy (XPS), small-angle X-ray scattering (SAXS), and X-ray diffraction. The synthesized nanoporous Mg is attractive for energy conversion and storage applications. Here, we show that it can produce hydrogen on-demand by hydrolysis with pure water and that it can also be used as a high-capacity lithium-ion battery anode.

Sub-100 mA/cm2 CO2-to-CO Reduction Current Densities in Hierarchical Porous Gold Electrocatalysts Made by Direct Ink Writing and Dealloying.

Abstract: While most research efforts on CO2-to-CO reduction electrocatalysts focus on boosting their selectivity, the reduction rate, directly proportional to the reduction current density, is another critical parameter to be considered in practical applications. This is because mass transport associated with the diffusion of reactant/product species becomes a major concern at a high reduction rate. Nanostructured Au is a promising CO2-to-CO reduction electrocatalyst for its very high selectivity. However, the CO2-to-CO reduction current density commonly achieved in conventional nanostructured Au electrocatalysts is relatively low (in the range of 1-10 mA/cm2) for practical applications. In this work, we combine direct ink writing-based additive manufacturing and dealloying to design a robust hierarchical porous Au electrocatalyst to improve the mass transport and achieve high CO2-to-CO reduction current densities on the order of 64.9 mA/cm2 with CO partial current density of 33.8 mA/cm2 at 0.55 V overpotential using an H-cell configuration. Although the current density achieved in our robust hierarchical porous Au electrocatalyst is one order of magnitude higher than the one achieved in conventional nanostructured electrocatalysts, we found that the selectivity of our system is relatively low, namely 52%, which suggests that mass transport remains a critical issue despite the hierarchical porous architecture. We further show that the bulk dimension of our electrocatalyst is a critical parameter governing the interplay between selectivity and reduction rate. The insights gained in this work shed new light on the design of electrocatalysts toward scale-up CO2 reduction and beyond.

Nanoporous Metals: From Plasmonic Properties to Applications in Enhanced Spectroscopy and Photocatalysis.

Abstract: The field of plasmonics is capable of enabling interesting applications in different wavelength ranges, spanning from the ultraviolet up to the infrared. The choice of plasmonic material and how th...

Scaling behavior of stiffness and strength of hierarchical network nanomaterials.

Abstract: Structural hierarchy can enhance the mechanical behavior of materials and systems. This is exemplified by the fracture toughness of nacre or enamel in nature and by human-made architected microscale network structures. Nanoscale structuring promises further strengthening, yet macroscopic bodies built this way contain an immense number of struts, calling for scalable preparation schemes. In this work, we demonstrated macroscopic hierarchical network nanomaterials made by the self-organization processes of dealloying. Their hierarchical architecture affords enhanced strength and stiffness at a given solid fraction, and it enables reduced solid fractions by dealloying. Scaling laws for the mechanics and atomistic simulation support the observations. Because they expose the systematic benefits of hierarchical structuring in nanoscale network structures, our materials may serve as prototypes for future lightweight structural materials.

Monolithic Nanoporous Zn Anode for Rechargeable Alkaline Batteries.

Abstract: The fabrication of monolithic nanoporous zinc bears its significance in safe and inexpensive energy storage; it can provide the much needed electrical conductivity and specific area in a practical alkaline battery to extend the short cycle life of a zinc anode. Although this type of structure has been routinely fabricated by dealloying, that is, the selective dissolution of an alloy, it has not led to a rechargeable zinc anode largely because the need for more reactive metal as the dissolving component in dealloying limits the choices of alloy precursors. Here, we apply the mechanism of dealloying, percolation dissolution, to design a process of reduction-induced decomposition of a zinc compound (ZnCl2) for nanoporous zinc. Using naphthalenide solution, we confine the selective dissolution of chloride to the compound/electrolyte interface, triggering the spontaneous formation of a network of 70 nm wide percolating zinc ligaments that retain the shape of a 200 μm thick monolith. We further reveal that this structure, when electrochemically oxidized and reduced in an alkaline electrolyte, undergoes surface-diffusion-controlled coarsening toward a quasi-steady-state with a length scale of ∼500 nm. The coarsening dynamics preserves the continuous zinc phase, enabling its uniform reaction and 200 cycles of stable performance at 40% depth of discharge (328 mAh/g) in a Ni-Zn battery.

Raising the COx methanation activity of a ru/γ‐Al2O3 catalyst by activated modification of metal–support interactions

Abstract: Ru/Al2 O3 is a highly stable, but less active catalyst for methanation reactions. Herein we report an effective approach to significantly improve its performance in the methanation of CO2 /H2 mixtures. Highly active and stable Ru/γ-Al2 O3 catalysts were prepared by high-temperature treatment in the reductive reaction gas. Operando/in situ spectroscopy and STEM imaging reveals that the strongly improved activity, by factors of 5 and 14 for CO and CO2 methanation, is accompanied by a flattening of the Ru nanoparticles and the formation of highly basic hydroxylated alumina sites. We propose a modification of the metal-support interactions (MSIs) as the origin of the increased activity, caused by modification of the Al2 O3 surface in the reductive atmosphere and an increased thermal mobility of the Ru nanoparticles, allowing their transfer to modified surface sites.