Activated graphene as a cathode material for Li-ion hybrid supercapacitors.

Chemically activated graphene ('activated microwave expanded graphite oxide', a-MEGO) was used as a cathode material for Li-ion hybrid supercapacitors. The performance of a-MEGO was first verified with Li-ion electrolyte in a symmetrical supercapacitor cell. Hybrid supercapacitors were then constructed with a-MEGO as the cathode and with either graphite or Li(4)Ti(5)O(12) (LTO) for the anode materials. The results show that the activated graphene material works well in a symmetrical cell with the Li-ion electrolyte with specific capacitances as high as 182 F g(-1). In a full a-MEGO/graphite hybrid cell, specific capacitances as high as 266 F g(-1) for the active materials at operating potentials of 4 V yielded gravimetric energy densities for a packaged cell of 53.2 W h kg(-1).

Synthesis and antitumor activity of novel thermosensitive platinum(II)-cyclotriphosphazene conjugates.

Thermosensitive cyclotriphosphazenes bearing alkoxy poly(ethylene glycol) and amino acid esters as side groups could be functionalized to chelate the antitumor (diamine)platinum(II) moiety through the dicarboxylate group of the amino acid substituent on the cyclic phosphazene ring. Surprisingly, like the precursor cyclotriphosphazenes, these (diamine)platinum(II)-cyclotriphosphazene conjugates were also found to exhibit variable lower critical solution temperatures (LCST) in the wide range of 12 to 92 degrees C. Furthermore, the present conjugates have shown outstanding in vitro and in vivo antitumor activities due to controlled release of the antitumor (diamine)platinum(II) moiety with hydrolytic degradation of the phosphazene ring. A few of these conjugates have shown LCSTs below body temperature, and it has been shown from a model animal experiment that the conjugates with a LCST below body temperature may be applied to local drug delivery by direct intratumoral injection.

Chemical structures of hydrazine-treated graphene oxide and generation of aromatic nitrogen doping.

Chemically modified graphene platelets, produced via graphene oxide, show great promise in a variety of applications due to their electrical, thermal, barrier and mechanical properties. Understanding the chemical structures of chemically modified graphene platelets will aid in the understanding of their physical properties and facilitate development of chemically modified graphene platelet chemistry. Here we use (13)C and (15)N solid-state nuclear magnetic resonance spectroscopy and X-ray photoelectron spectroscopy to study the chemical structure of (15)N-labelled hydrazine-treated (13)C-labelled graphite oxide and unlabelled hydrazine-treated graphene oxide, respectively. These experiments suggest that hydrazine treatment of graphene oxide causes insertion of an aromatic N(2) moiety in a five-membered ring at the platelet edges and also restores graphitic networks on the basal planes. Furthermore, density-functional theory calculations support the formation of such N(2) structures at the edges and help to elucidate the influence of the aromatic N(2) moieties on the electronic structure of chemically modified graphene platelets.

Simultaneous transfer and doping of CVD-grown graphene by fluoropolymer for transparent conductive films on plastic.

Chemical doping can decrease sheet resistance of graphene while maintaining its high transparency. We report a new method to simultaneously transfer and dope chemical vapor deposition grown graphene onto a target substrate using a fluoropolymer as both the supporting and doping layer. Solvent was used to remove a significant fraction of the supporting fluoropolymer, but residual polymer remained that doped the graphene significantly. This contrasts with a more widely used supporting layer, polymethylmethacrylate, which does not induce significant doping during transfer. The fluoropolymer doping mechanism can be explained by the rearrangement of fluorine atoms on the graphene basal plane caused by either thermal annealing or soaking in solvent, which induces ordered dipole moments near the graphene surface. This simultaneous transfer and doping of the graphene with a fluoropolymer increases the carrier density significantly, and the resulting monolayer graphene film exhibits a sheet resistance of ∼320 Ω/sq. Finally, the method presented here was used to fabricate flexible and a transparent graphene electrode on a plastic substrate.

Unilamellar nanosheet of layered manganese cobalt nickel oxide and its heterolayered film with polycations.

The exfoliation of layered Li[Mn(1/3)Co(1/3)Ni(1/3)]O(2) into individual monolayers could be achieved through the intercalation of quaternary tetramethylammonium (TMA(+)) ions into protonated metal oxide. An effective exfoliation occurred when the TMA(+)/H(+) ratio was 0.5-50. Reactions outside this range produced no colloidal suspension, but all the manganese cobalt nickel oxides precipitated. Atomic force microscopy and transmission electron microscopy clearly demonstrated that exfoliated manganese cobalt nickel oxide nanosheets have a nanometer-level thickness, underscoring the formation of unilamellar nanosheets. The maintenance of the hexagonal atomic arrangement of the manganese cobalt nickel oxide layer upon the exfoliation was confirmed by selected area electron diffraction analysis. According to diffuse reflectance ultraviolet--visible spectroscopy, the exfoliated manganese cobalt nickel oxides displayed distinct absorption peaks at approximately 354 and approximately 480 nm corresponding to the d-d transitions of octahedral metal ions, which contrasted with the featureless spectrum of the pristine metal oxide. In the light of zeta potential data showing the negative surface charge of manganese cobalt nickel oxide nanosheets, a heterolayered film of manganese cobalt nickel oxide and conductive polymers could be prepared through the successive coating process with colloidal suspension and polycations. The UV--vis and X-ray diffraction studies verified the layer-by-layer ordered structure of the obtained heterolayered film, respectively.