Graphene and its derivatives are attractive for electrocatalytical application in fuel cells because of their unique structures and electronic properties. The electrocatalytical mechanism of nitrogen doped graphene in acidic environment was studied by using density functional theory (DFT). The simulations demonstrate that the oxygen reduction reaction (ORR) on N-doped graphene is a direct four-electron pathway, which is consistent with the experimental observations. The energy calculated for each ORR step shows that the ORR can spontaneously occur on the N-graphene. The active catalytical sites on single nitrogen doped graphene are identified, which have either high positive spin density or high positive atomic charge density. The nitrogen doping introduces asymmetry spin density and atomic charge density, making it possible for N-graphene to show high electroncatalytic activities for the ORR.

The cathodic oxygen reduction reaction (ORR) is an important process in fuel cells and metal-air batteries. [1][2][3] Although Pt-based electrocatalysts have been commonly used in commercial fuel cells owing to their relatively low overpotential and high current density, they still suffer from serious intermediate tolerance, anode crossover, sluggish kinetics, and poor stability in an electrochemical environment. This, together with the high cost of Pt and its limited nature reserves, has prompted the extensive search for alternative low-cost and high-performance ORR electrocatalysts. In this context, carbon-based metal-free ORR electrocatalysts have generated a great deal of interest owing to their low-cost, high electrocatalytic activity and selectivity, and excellent durability. [4][5][6][7][8][9] Of particular interest, we have previously prepared vertically aligned nitrogendoped carbon nanotubes (VA-NCNTs) as ORR electrocatalysts, which are free from anode crossover and CO poisoning and show a threefold higher catalytic activity and better durability than the commercial Pt/C catalyst. [4] Quantum mechanics calculations [4] indicate that the enhanced catalytic activity of VA-NCNTs toward ORR can be attributed to the electron-accepting ability of the nitrogen species, which creates net positive charges on the CNT surface to enhance oxygen adsorption and to readily attract electrons from the anode for facilitating the ORR. Uncovering this new ORR mechanism in nitrogen-doped carbon nanotube electrodes is significant as the same principle could be applied to the development of various other metal-free efficient ORR catalysts for fuel-cell applications and even beyond fuel cells. Indeed, recent intensive research efforts in developing metal-free ORR electrocatalysts have led to a large variety of carbon-based metal-free ORR electrocatalysts, including heteroatom (N, B, or P)-doped carbon nanotubes, graphene, and graphite. [4][5][6][7][8][9][10][11][12][13][14] More recently, we have successfully synthesized vertically aligned carbon nanotubes co-doped with N and B (VA-BCN) and demonstrated a significantly improved electrocatalytic activity toward the ORR, with respect to CNTs doped with either N or B, only due to a synergetic effect arising from the N and B co-doping. [15] However, most of the reported carbon-based ORR electrocatalysts (particularly, heteroatom-doped nanotubes and graphene) were produced by chemical vapor-deposition (CVD) processes involving vacuum-based elaborate and careful fabrication, which are often too tedious and too expensive for mass production. As demonstrated in this study, therefore, it is of great importance to develop a facile approach to BCN graphene as low-cost and efficient ORR electrocatalysts. The recent availability of solution-exfoliated graphite oxide (GO) [16] allows the mass production of graphene and derivatives by conventional physicochemical treatments of GO.Herein, we have developed a facile approach to metalfree BCN graphene of tunable B/N co-doping levels as efficient...

To replace precious platinum (Pt)-based electrocatalysts for cathodic oxygen reduction reaction (ORR), edge-selectively sulfurized graphene nanoplatelets (SGnP) are synthesized as efficient metal-free electrocatalysts simply by ball-milling pristine graphite in the presence of sulfur (S8 ). The resultant SGnPs exhibit remarkable electrocatalytic activity toward ORR with better tolerance to methanol crossover/CO poisoning effects and longer-term stability than those of pristine graphite and commercial Pt/C electrocatalysts. Edge-Selectively Sulfurized Graphene Nanoplatelets as Efficient Metal-Free Electrocatalysts for Oxygen Reduction Reaction: The Electron Spin Effect.

With global warming forecast to continue into the foreseeable future, heat waves are very likely to increase in both frequency and intensity. In urban regions, these future heat waves will be exacerbated by the urban heat island effect, and will have the potential to negatively influence the health and welfare of urban residents. In order to investigate the health effects of the urban heat island (UHI) in Shanghai, China, 30 years of meteorological records (1975-2004) were examined for 11 first- and second-order weather stations in and around Shanghai. Additionally, automatic weather observation data recorded in recent years as well as daily all-cause summer mortality counts in 11 urban, suburban, and exurban regions (1998-2004) in Shanghai have been used. The results show that different sites (city center or surroundings) have experienced different degrees of warming as a result of increasing urbanization. In turn, this has resulted in a more extensive urban heat island effect, causing additional hot days and heat waves in urban regions compared to rural locales. An examination of summer mortality rates in and around Shanghai yields heightened heat-related mortality in urban regions, and we conclude that the UHI is directly responsible, acting to worsen the adverse health effects from exposure to extreme thermal conditions.

Highlights d Development of two potent FTO inhibitors with IC 50 values in the low nanomolar range d KD of FTO or pharmacological inhibition of FTO suppresses LSC/LIC self-renewal d Targeting FTO suppresses immune checkpoint gene expression and immune evasion d Targeting FTO by potent inhibitors holds therapeutic promise against various cancers

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Oxygen reduction reaction/oxygen evolution reaction (ORR/OER) catalytic activities of p-orbital heteroatom-doped carbon nanomaterials are demonstrated to correlate to the combination of the electron affinity and electronegativity of doping elements, which serves as an activity descriptor for the entire family of p-block element dopants. Such a descriptor has predictive power and enables effective design of new bifunctional catalysts with enhanced ORR/OER activities.

Density functional theory (DFT) was applied to study sulfur-doped graphene clusters as oxygen reduction reaction (ORR) cathode catalysts for fuel cells. Several sulfurdoped graphene clusters with/without Stone−Wales defects were investigated and their electronic structures, reaction free energy, transition states, and energy barriers were calculated to predict their catalytic properties. The results show that sulfur atoms could be adsorbed on the graphene surface, substitute carbon atoms at the graphene edges in the form of sulfur/ sulfur oxide, or connect two graphene sheets by forming a sulfur cluster ring. These sulfur-doped graphene clusters with sulfur or sulfur oxide locating at graphene edges show electrocatalytic activity for ORR. Catalytic active sites distribute at the zigzag edge or the neighboring carbon atoms of doped sulfur oxide atoms, which possess large spin or charge density. For those being the active catalytic sites, sulfur atoms with the highest charge density take a two-electron transfer pathway while the carbon atoms with high spin or charge density follow a four-electron transfer pathway. It was predicted from the reaction energy barriers that the sulfur-doped graphene could show ORR catalytic properties comparable to platinum. The prediction is consistent with the experimental results on S-doped graphene.