Due to an oversight of the editorial office, a mistake was introduced in the references on page 3919, right column, at the start of the fourth paragraph. In the published paper the text segment on page 3919 reads: As mentioned, graphene can be grown on metal surfaces by surface segregation of carbon or by decomposition of hydrocarbons. However, this technique is only practical for graphene production if the as-grown graphene can be transferred from the metal substrates to other substrates, which looks straightforward but only was realized for multilayer and non-uniform films recently with Ni [160-162] and for uniform monolayer graphene, with Cu. [17] However, reference 160 does not relate to graphene segregation on metal surfaces. The authors first to report this technique were Qingkai Yu and co-workers as described in reference 246. Consequently, the start of the fourth paragraph on page 3919 should be corrected to read as follows: As mentioned, graphene can be grown on metal surfaces by surface segregation of carbon or by decomposition of hydrocarbons. However, this technique is only practical for graphene production if the as-grown graphene can be transferred from the metal substrates to other sub-strates, which looks straightforward but only was realized for multilayer and non-uniform films recently with Ni, [246,161,162] and for uniform monolayer graphene, with Cu. [17] The editorial office apologizes for any inconvenience caused. In addition, reference 160 was not published in 2009, so reference 160 should read: [160] J.

No abstract

We present two different ways to fabricate nitrogen-doped graphene (N-graphene) and demonstrate its use as a metal-free catalyst to study the catalytic active center for the oxygen reduction reaction (ORR). N-graphene was produced by annealing of graphene oxide (G-O) under ammonia or by annealing of a N-containing polymer/reduced graphene oxide (RG-O) composite (polyaniline/RG-O or polypyrrole/ RG-O). The effects of the N precursors and annealing temperature on the performance of the catalyst were investigated. The bonding state of the N atom was found to have a significant effect on the selectivity and catalytic activity for ORR. Annealing of G-O with ammonia preferentially formed graphitic N and pyridinic N centers, while annealing of polyaniline/RG-O and polypyrrole/RG-O tended to generate pyridinic and pyrrolic N moieties, respectively. Most importantly, the electrocatalytic activity of the catalyst was found to be dependent on the graphitic N content which determined the limiting current density, while the pyridinic N content improved the onset potential for ORR. However, the total N content in the graphene-based non-precious metal catalyst does not play an important role in the ORR process.

No abstract

Chemically modified graphene (CMG) nanoplatelets have shown great promise in various applications due to their electrical properties and high surface area. Chemical doping is one of the most effective methods to tune the electronic properties of graphene materials. In this work, novel B-doped nanoplatelets (borane-reduced graphene oxide, B-rG-O) were produced on a large scale via the reduction of graphene oxide by a borane-tetrahydrofuran adduct under reflux, and their use for supercapacitor electrodes was studied. This is the first report on the production of B-doped graphene nanoplatelets from a solution process and on the use of B-doped graphene materials in supercapacitors. The B-rG-O had a high specific surface area of 466 m(2)/g and showed excellent supercapacitor performance including a high specific capacitance of 200 F/g in aqueous electrolyte as well as superior surface area-normalized capacitance to typical carbon-based supercapacitor materials and good stability after 4500 cycles. Two- and three-electrode cell measurements showed that energy storage in the B-rG-O supercapacitors was contributed by ion adsorption on the surface of the nanoplatelets in addition to electrochemical redox reactions.