Nitrate is ar aw ingredient for the production of fertilizer,g unpowder,a nd explosives.D eveloping an alternative approach to activate the NNbond of naturally abundant nitrogen to form nitrate under ambient conditions will be of importance.Herein, pothole-rich WO 3 was used to catalyse the activation of N Nc ovalent triple bonds for the direct nitrate synthesis at room temperature.T he pothole-rich structure endues the WO 3 nanosheet more dangling bonds and more easily excited high momentum electrons,w hicho vercome the two major bottlenecks in NNb ond activation, that is,p oor binding of N 2 to catalytic materials and the high energy involved in this reaction. The average rate of nitrate production is as high as 1.92 mg g À1 h À1 under ambient conditions,without any sacrificial agent or precious-metal co-catalysts.M ore generally,t he concepts will initiate an ew pathwayf or triggering inert catalytic reactions.

Under the double pressure of both the energy crisis and environmental pollution, the exploitation and utilization of hydrogen, a clean and renewable power resource, has become an important trend in the development of sustainable energy-production and energy-consumption systems. In this regard, the electrocatalytic hydrogen evolution reaction (HER) provides an efficient and clean pathway for the mass production of hydrogen fuel and has motivated the design and construction of highly active HER electrocatalysts of an acceptable cost. In particular, graphene-based electrocatalysts commonly exhibit an enhanced HER performance owing to their distinctive structural merits, including a large surface area, high electrical conductivity, and good chemical stability. Considering the rapidly growing research enthusiasm for this topic over the last several years, herein, a panoramic review of recent advances in graphene-based electrocatalysts is presented, covering various advanced synthetic strategies, microstructural characterizations, and the applications of such materials in HER electrocatalysis. Lastly, future perspectives on the challenges and opportunities awaiting this emerging field are proposed and discussed.

The design and construction of high-performance platinum-based electrode catalysts with acceptable cost are the keys to advances in the field of direct methanol fuel cells (DMFCs). Herein, we report an efficient bottom-up approach for the large-scale production of ultrafine Pt NP-decorated 3D hybrid architectures by employing graphene (RGO) and MXene (Ti 3 C 2 T x ) nanosheets as cobuilding blocks. Benefiting from their distinct structural merits, such as highly interconnected porous carbon networks, large specific surface areas, homogeneous metallic Pt dispersion, and good electron conductivity, the resulting 3D Pt/RGO−Ti 3 C 2 T x architectures express surprisingly high catalytic activity, reliable long-term stability, and strong poison tolerance as they are utilized as anode DMFC catalysts, which are more competitive than those for conventional Pt catalysts supported by carbon black, carbon nanotube, RGO, and Ti 3 C 2 T x materials. Density functional theory calculation further reveals an optimized band structure of the RGO− Ti 3 C 2 T x support as well as its strong electronic interactions with Pt NPs, which are essential for the exceptional electrocatalytic properties toward methanol oxidation reaction.

A novel 1D metal-organic nanotube, exhibiting reversible and fast adsorption of the (H2O)12 cluster, has been synthesized and characterized.