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Koon-Gee Neoh

Publications and source records attributed to Koon-Gee Neoh.

7 recordsLinked to original sources
PubMed2007

Nonvolatile polymer memory device based on bistable electrical switching in a thin film of poly(N-vinylcarbazole) with covalently bonded C60.

A functional polymer (PVK-C60), containing carbazole moieties (electron donors) and fullerene moieties (electron-acceptors) in a molar ratio of about 100:1, was synthesized via covalent tethering of C60 to poly(N-vinylcarbazole) (PVK). The molecular structure and composition of PVK-C60 were characterized by FTIR, Raman, and UV-vis absorption spectroscopy, gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CyV). The C60-modified PVK exhibited an enhanced glass-transition temperature (Tg = 226 degrees C) and good solubility in organic solvents such as toluene, tetrahydrofuran, chloroform, and N,N-dimethylformamide (DMF). It could be cast into transparent films from solutions. For a thin film of PVK-C60 sandwiched between an indium tin oxide (ITO) electrode and an Al electrode (ITO/PVK-C60/Al), the device behaved as nonvolatile flash (rewritable) memory with accessible electronic states that could be written, read, and erased. The polymer memory exhibited an ON/OFF current ratio of more than 105 and write/erase voltages around -2.8 V/+3.0 V. Both the ON and OFF states were stable under a constant voltage stress of -1 V for 12 h and survived up to 108 read cycles at -1 V under ambient conditions.

Journal Article↗
PubMed2006

Bistable electrical switching and memory effects in a thin film of copolymer containing electron donor-acceptor moieties and europium complexes.

A nonconjugated methacrylate copolymer (PCzOxEu) containing carbazole moieties (electron donors), 1,3,4-oxadiazole moieties (electron acceptors), and europium complexes in the pendant groups was synthesized via free radical copolymerization of methacrylate monomers containing the respective functional groups. The molecular structure and composition of PCzOxEu was characterized by elemental analysis, FT-IR, 1H NMR, 13C NMR, UV-vis absorption and fluorescence spectroscopies, gel permeation chromatography (GPC), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CyV). The resulting copolymer exhibited a relatively high glass transition temperature (Tg approximately 125 degrees C) and good solubility in common organic solvents. It could be cast into transparent films from solutions. For a thin film of PCzOxEu sandwiched between an indium-tin oxide (ITO) electrode and an Al electrode (ITO/PCzOxEu/Al), the structure behaved as a nonvolatile flash (rewritable) memory with accessible electronic states that could be written, read, and erased. The polymer memory exhibited an ON/OFF current ratio up to 10(5), switching response time of approximately 1.5 micros, more than 10(6) read cycles, retention time of more than 8 h, and write/erase voltages of about 4.4 V/-2.8 V under ambient conditions. The roles of oxadiazole moieties in improving the response time and retention time of the memory device were elucidated from the molecular simulation results.

Journal Article↗
PubMed2006

QCM-D analysis of binding mechanism of phage particles displaying a constrained heptapeptide with specific affinity to SiO2 and TiO2.

A growing number of peptides capable of specifically recognizing inorganic materials have been reported, incrementally increasing the potential to harness peptides as a biological linker to bridge biomolecules and inorganic materials at nanometer scale. In this study, we identified disulfide bond constrained heptapeptides with specific binding affinity to SiO2 and TiO2 using a phage display technique. Interestingly, two of the phage surface displayed peptides enriched with basic amino acid residues, STB1 (HKKPSKS) and STB2 (TKRNNKR), showed a cross binding affinity to both metal oxides. To understand the underlying binding mechanism, binding behaviors of phage particles harboring the STB1 (a high-frequency heptapeptide exhibiting dual binding affinity to both metal oxides) were investigated in a wide pH range using quartz crystal microbalance with energy dissipation measurement (QCM-D). It was found that the binding of STB1-harboring phages to the two metal oxides was clearly mediated by the peptide moiety displayed on the phage surface in a pH-dependent manner, indicating that the binding is largely governed by electrostatic interaction. Furthermore, the interpretation of QCM-D signals (i.e., frequency shift and dissipation shift), with the aid of AFM image analysis of the phage particles bound on the surface of the two metal oxides, elucidated whether the nature of phage (or the displayed peptide) binding to the metal oxides is largely specific or nonspecific.

Amino Acid Sequence↗
PubMed2006

Synthesis and dynamic random access memory behavior of a functional polyimide.

The device under testing was a plastic dynamic random access memory based on a donor-functionalized polyimide (TP6F-PI), which exhibited the ability to write, read, erase, and refresh the electrical states. The device had an ON/OFF current ratio up to 105, promising minimal misreading error. Both the on and off states were stable under a constant voltage stress of 1 V and survived up to 108 read cycles at 1 V.

Journal Article↗
PubMed2006

pH- and temperature-responsive hydrogels from crosslinked triblock copolymers prepared via consecutive atom transfer radical polymerizations.

Well-defined poly((2-dimethyl amino)ethyl methacrylate-co-2-hydroxyethyl methacrylate)-b-poly(N-isopropylacrylamide)-b-poly((2-dimethyl amino)ethyl methacrylate-co-2-hydroxyethyl methacrylate), or P(DMAEMA-co-HEMA)-b-P(NIPAAm)-b-P(DMAEMA-co-HEMA), triblock copolymers were synthesized by consecutive atom transfer radical polymerizations (ATRPs), using ethylene glycol di-2-bromoisobutyrate (Br-EG-Br) as the starting ATRP initiator. The hydroxyl groups of the incorporated HEMA units were used as crosslinking sites for the preparation of smart hydrogels. The so-prepared hydrogels exhibited both temperature- and pH-sensitive behavior derived, respectively, and independently, from the P(NIPAAm) blocks and P(DMAEMA) units, in the crosslinked matrices. The hydrogels exhibited a lower critical solution temperature (LCST) of 31-32 degrees C in aqueous media of pH 1-7, not unlike that of the P(NIPAAm) homopolymer. The swelling ratios and swelling/deswelling kinetics of the hydrogels depended strongly on pH and temperature of the medium. The copolymers were characterized by gel-permeation chromatography, X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FTIR) spectroscopy, and (1)H nuclear magnetic resonance ((1)H NMR) spectroscopy. The resultant stimuli-responsive hydrogels were characterized by differential scanning calorimetry (DSC). These stimuli-responsive hydrogels will have potential applications in biomedical areas, such as tissue engineering and drug delivery.

Hydrogels↗