Mesoporous carbon nitrides (MCN) with C 3 N 4 stoichiometry could find applications in fields ranging from catalysis,sensing, and adsorption-separation to biotechnology. The extension of the synthesis of MCN with different nitrogen contents and chemical structures promises access to aw ider range of applications.H erein we prepare mesoporous C 3 N 5 with acombined triazole and triazine framework via asimple self-assembly of 5-amino-1H-tetrazole (5-ATTZ). We are able to hybridizet hese nanostructures with graphene by using graphene-mesoporous-silica hybrids as at emplate to tune the electronic properties.D FT calculations and spectroscopic analyses clearly demonstrate that the C 3 N 5 consists of 1triazole and 2triazine moieties.T he triazole-based mesoporous C 3 N 5 and its graphene hybrids are found to be highly active for oxygen reduction reaction (ORR) with ah igher diffusionlimiting current density and ad ecreased overpotential than those of bulk g-C 3 N 4 .

Carbon nitrides with a high N/C atomic ratio (>2) are expected to offer superior basicity and unique electronic properties. However, the synthesis of these nanostructures is highly challenging since many parts of the CN frameworks in the carbon nitride should be replaced with thermodynamically less stable NN frameworks as the nitrogen content increases. Thermodynamically stable C3N7 and C3N6 with an ordered mesoporous structure are synthesized at 250 and 300 °C respectively via a pyrolysis process of 5‐amino‐1H‐tetrazole (5‐ATTZ). Polymerization of the precursor to the ordered mesoporous C3N7 and C3N6 is clearly proved by X‐ray and electron diffraction analyses. A combined analysis including diverse spectroscopy and FDMNES and density functional theory (DFT) calculations demonstrates that the NN bonds are stabilized in the form of tetrazine and/or triazole moieties in the C3N7 and C3N6. The ordered mesoporous C3N7 represents the better oxygen reduction reaction (ORR) performances (onset potential: 0.81 V vs reversible hydrogen electrode (RHE), electron transfer number: 3.9 at 0.5 V vs RHE) than graphitic carbon nitride (g‐C3N4) and the ordered mesoporous C3N6. The study on the mechanism of ORR suggests that nitrogen atoms in the tetrazine moiety of the ordered mesoporous C3N7 act as active sites for its improved ORR activity.

Mesoporous carbon nitride (MCN) with well-ordered porous structures is a promising anode material for secondary ion batteries owing to their unique physico-and electrochemical properties. However, the practical application of these MCNs in sodium-ion batteries (SIBs) is still limited because of their confined interlayer distance, which results in restricted accommodation of Na ions inside the lattice. Here, we report on the synthesis of highly ordered sulfur-doped MCN (S-MCN) through a hard template approach by employing dithiooxamide (DTO) as a single molecular precursor containing carbon, nitrogen, and sulfur elements. The interlayer distance of carbon nitride is significantly expanded upon the introduction of larger S ions on the MCN lattice, which enables high capability of Na ion accommodation. We also demonstrate through the first-principles density functional theory calculation that the present S-MCN is highly optimized not only for the chemical structure but also for uptaking abundant Na ions with high adsorption energy. The specific discharge capacity of SIBs appears to be remarkably enhanced for S-MCN (304.2 mA h g −1 ) compared to the nonporous S-CN (167.9 mA h g −1 ) and g-C 3 N 4 (5.4 mA h g −1 ), highlighting the pivotal roles of the highly ordered mesoporous structure and S-doping in enhancing the electrochemical functionality of carbon nitride as an anode material for SIBs.

Mesoporous carbon nitrides (MCN) with C3N4 stoichiometry could find applications in fields ranging from catalysis, sensing, and adsorption–separation to biotechnology. The extension of the synthesis of MCN with different nitrogen contents and chemical structures promises access to a wider range of applications. Herein we prepare mesoporous C3N5 with a combined triazole and triazine framework via a simple self‐assembly of 5‐amino‐1H‐tetrazole (5‐ATTZ). We are able to hybridize these nanostructures with graphene by using graphene–mesoporous‐silica hybrids as a template to tune the electronic properties. DFT calculations and spectroscopic analyses clearly demonstrate that the C3N5 consists of 1 triazole and 2 triazine moieties. The triazole‐based mesoporous C3N5 and its graphene hybrids are found to be highly active for oxygen reduction reaction (ORR) with a higher diffusion‐limiting current density and a decreased overpotential than those of bulk g‐C3N4.

The existence of many molecules in the form of clathrate hydrates (CHs) in ultrahigh vacuum (UHV) and cryogenic conditions has not been explored adequately. In the present study, a detailed investigation by reflection absorption infrared spectroscopy confirmed that the three phases of ethane, i.e., amorphous, crystalline, and CH, coexist in a vapor-deposited ethane−water mixture at 60 K in UHV. Experiments were conducted with vapor-deposited ice films at 10 K, which were annealed to 60 K for tens of hours, and the IR spectral evolution was monitored systematically. Upon maintaining the system at 60 K, three phases of ethane were seen to coexist, but a gradual increase in the hydrate phase was noticed. The evolution of ethane CH from the amorphous ethane−water ice mixture was observed for the very first time in UHV under cryogenic conditions. The formation of the CH was further confirmed by temperature-programmed desorption (TPD) mass spectrometry. Quantum chemical calculation suggested the formation of 5 12 6 2 cage of structure I CH in the ice matrix. The formation of ethane CH in a thin ice film at such a low temperature under UHV suggests its existence in the cometary environment.