Boron-doped graphene with different boron structures was rationally synthesized to enhance the adsorption of N 2 , thus enabling an efficient metal-free electrocatalyst for electrochemical N 2 reduction in aqueous solution at ambient conditions. At a doping level of 6.2%, boron-doped graphene achieved a NH 3 production rate of 9.8 mg$hr À1 $cm À2 and an excellent faradic efficiency (10.8% at À0.5 V versus reversible hydrogen electrode).

The rapid increase of the CO concentration in the Earth's atmosphere has resulted in numerous environmental issues, such as global warming, ocean acidification, melting of the polar ice, rising sea level, and extinction of species. To search for suitable and capable catalytic systems for CO conversion, electrochemical reduction of CO (CO RR) holds great promise. Emerging heterogeneous carbon materials have been considered as promising metal-free electrocatalysts for the CO RR, owing to their abundant natural resources, tailorable porous structures, resistance to acids and bases, high-temperature stability, and environmental friendliness. They exhibit remarkable CO RR properties, including catalytic activity, long durability, and high selectivity. Here, various carbon materials (e.g., carbon fibers, carbon nanotubes, graphene, diamond, nanoporous carbon, and graphene dots) with heteroatom doping (e.g., N, S, and B) that can be used as metal-free catalysts for the CO RR are highlighted. Recent advances regarding the identification of active sites for the CO RR and the pathway of reduction of CO to the final product are comprehensively reviewed. Additionally, the emerging challenges and some perspectives on the development of heteroatom-doped carbon materials as metal-free electrocatalysts for the CO RR are included.

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Aluminum-ion batteries (AIBs) are regarded as viable alternatives to lithium-ion technology because of their high volumetric capacity, their low cost, and the rich abundance of aluminum. However, several serious drawbacks of aqueous systems (passive film formation, hydrogen evolution, anode corrosion, etc.) hinder the large-scale application of these systems. Thus, nonaqueous AIBs show incomparable advantages for progress in large-scale electrical energy storage. However, nonaqueous aluminum battery systems are still nascent, and various technical and scientific obstacles to designing AIBs with high capacity and long cycling life have not been resolved until now. Moreover, the aluminum cell is a complex device whose energy density is determined by various parameters, most of which are often ignored, resulting in failure to achieve the maximum performance of the cell. The purpose here is to discuss how to further develop reliable nonaqueous AIBs. First, the current status of nonaqueous AIBs is reviewed based on statistical data from the literature. The influence of parameters on energy density is analyzed, and the current situation and existing problems are summarized. Furthermore, possible solutions and concerns regarding the construction of reliable nonaqueous AIBs are comprehensively discussed. Finally, future research directions and prospects in the aluminum battery field are proposed.

The alpha-Fe(2)O(3) with various morphologies has been successfully synthesized via an ionic liquid-assisted hydrothermal synthetic method. The samples are characterized by X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscope (FE-SEM), transmission electron microscopy, and high-resolution transmission electron microscopy. The results indicate that the as-prepared samples are alpha-Fe(2)O(3) nanoparticles, mesoporous hollow microspheres, microcubes, and porous nanorods. The effects of the ionic liquid 1-n-butyl-3-methylimidazolium chloride ([bmim][Cl]) on the formation of the alpha-Fe(2)O(3) with various morphologies have been investigated systematically. The proposed formation mechanisms have also been investigated on the basis of a series of FE-SEM studies of the products obtained at different durations. Because of the unique porous structure, the potential application in water treatment of the alpha-Fe(2)O(3) porous nanorods was investigated. The UV-vis measurements suggest that the as-synthesized pure alpha-Fe(2)O(3) with various morphologies possess different optical properties depending on the shape and size of the samples. The magnetic hysteresis measurements indicate the interesting magnetic property evolution in the as-prepared alpha-Fe(2)O(3) samples, which is attributed to the superstructure or the shape anisotropy of the samples. This method is expected to be a useful technique for controlling the diverse shapes of crystalline inorganic materials for a variety of applications, such as sensors, gas and heavy metal ion adsorbents, catalytic fields, hydrogen and Li ion storage, and controlled drug delivery, etc.