We report a novel microwave plasma enhanced chemical vapor deposition strategy for the efficient synthesis of multilayer graphene nanoflake films (MGNFs) on Si substrates. The constituent graphene nanoflakes have a highly graphitized knife‐edge structure with a 2–3 nm thick sharp edge and show a preferred vertical orientation with respect to the Si substrate as established by near‐edge X‐ray absorption fine structure spectroscopy. The growth rate is approximately 1.6 µm min−1, which is 10 times faster than the previously reported best value. The MGNFs are shown to demonstrate fast electron‐transfer (ET) kinetics for the Fe(CN)63−/4− redox system and excellent electrocatalytic activity for simultaneously determining dopamine (DA), ascorbic acid (AA) and uric acid (UA). Their biosensing DA performance in the presence of common interfering agents AA and UA is superior to other bare solid‐state electrodes and is comparable only to that of edge plane pyrolytic graphite. Our work here, establishes that the abundance of graphitic edge planes/defects are essentially responsible for the fast ET kinetics, active electrocatalytic and biosensing properties. This novel edge‐plane‐based electrochemical platform with the high surface area and electrocatalytic activity offers great promise for creating a revolutionary new class of nanostructured electrodes for biosensing, biofuel cells and energy‐conversion applications.
The first paragraph of the above mentioned article was accidentally deleted during preparation of the final version. The omitted first paragraph is shown here: Organic electronics has reached the market in a very short period of time, since the first organic light emitting device has been demonstrated. [1] Growth of organic thin films has been the focus of intensive investigations that in the recent years have gained knowledge about the involved mechanisms: substrate-molecule interaction versus molecule-molecule interaction, preparation parameters, substrate morphology (i.e., roughness, local defects, steps), and post growth treatment. [2-6] Here we investigate thin films of diindenoperylene deposited on Au(111) single crystals by using photoelectron emission microscopy (PEEM). We also discuss the effect of the growth on the film structure using the molecular orientation (i.e., the angle between the molecular axis and the substrate). The publisher apologizes for any inconvenience caused.
Growth and surface termination of a Fe 3 O 4 (111) thin film on a Pt(111) surface were examined by a combination of low-energy electron microscopy, selected area low-energy electron diffraction (LEED), and x-ray-induced photoemission electron microscopy. The film exhibits the predominance of one out of two possible rotational domains, independent of film thickness. The morphology strongly depends on preparation conditions, e.g., at high oxidation temperature FeO/Pt(111) domains are formed that prevent the closure of the thin film. Dynamical LEED analysis and spot-profile analysis LEED (SPA-LEED) show that the surface exposes 1 4 monolayer of Fe over a close-packed oxygen layer only when the sample is subsequently annealed in ultrahigh vacuum at 900 K. In contrast, the as-prepared films grown by oxidation at 1000 K and subsequent cooling down in oxygen, additionally exhibit small FeO x agglomerates that rest upon the canonical surface termination. Their formation as a function of the various preparation conditions of the thin film is discussed.
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