Search

Lithium-oxygen batteries (LOBs) and direct methanol fuel cells (DMFCs) are both attractive technologies for the development of future energy storage and conversion devices, while the lack of highly active electrocatalysts has largely hampered their large-scale commercial applications. In the present work, we have demonstrated the controllable synthesis of nitrogen and sulfur codoped graphene (NS-G) nanosheets via a simple and cost-effective approach. Owing to their distinctive structural advantages, such as large surface areas, good flexibility, coexistence of N and S atoms with tunable doping contents and positions, and high electrical conductivity, the obtained NS-G sheets exhibit low discharge-recharge voltage gaps and high round-trip efficiencies as well as exceptional rate capability when used as cathode materials for LOBs. Furthermore, the NS-G layers are also identified to be an ideal substrate for the decoration of ultrafine Pt nanoparticles. Benefiting from the synergetic effects, exceptional electrocatalytic properties including high activity, strong poison tolerance, and outstanding long-term stability are observed for the resulting Pt/NS-G hybrid toward methanol oxidation reaction, which are significantly superior to those for Pt/undoped graphene and commercial Pt/C catalysts. [ABSTRACT FROM AUTHOR]

Heterostructures of compositionally and electronically variant two-dimensional (2D) atomic layers are viable building blocks for ultrathin optoelectronic devices. We show that the composition of interfacial transition region between semiconducting WSe2 atomic layer channels and metallic NbSe2 contact layers can be engineered through interfacial doping with Nb atoms. WxNb1-xSe2 interfacial regions considerably lower the potential barrier height of the junction, significantly improving the performance of the corresponding WSe2-based field-effect transistor devices. The creation of such alloyed 2D junctions between dissimilar atomic layer domains could be the most important factor in controlling the electronic properties of 2D junctions and the design and fabrication of 2D atomic layer devices. [ABSTRACT FROM AUTHOR]

The practical recycling of carbon dioxide (CO2) by the electrochemical reduction route requires an active, stable, and affordable catalyst system. Although noble metals such as gold and silver have been demonstrated to reduce CO2 into carbon monoxide (CO) efficiently, they suffer from poor durability and scarcity. Here we report three-dimensional (3D) graphene foam incorporated with nitrogen defects as a metal-free catalyst for CO2 reduction. The nitrogen-doped 3D graphene foam requires negligible onset overpotential (-0.19 V) for CO formation, and it exhibits superior activity over Au and Ag, achieving similar maximum Faradaic efficiency for CO production (~85%) at a lower overpotential (-0.47 V) and better stability for at least 5 h. The dependence of catalytic activity on N-defect structures is unraveled by systematic experimental investigations. Indeed, the density functional theory calculations confirm pyridinic N as the most active site for CO2 reduction, consistent with experimental results. [ABSTRACT FROM AUTHOR]