In this study, a novel fibrous carbon nitride (FCN) was prepared from laminated covalent triazine framework (CTF) via pyrolysis, using functionalized 2,5-thiophenedicarboxylic acid and melamine as the precursors. A carbon vacancy was produced by two-step calcination in argon and air atmospheres. These carbon vacancies further exposed the edges and diffusion channels of the FCN nanofibers, which accelerated photogenerated charge transfer and provided more active sites. The FCN was characterized using various techniques and used for H₂ evolution under visible-light irradiation. The as-synthesized FCN exhibited excellent stability, and its photocatalytic activity for H₂ evolution under visible-light irradiation was 66 times higher than that of bare C₃N₄ (BCN), attaining a maximum H₂ evolution rate of 102.63 $\mathsf{\mu }$mol in 6 h. The FCN remained stable following visible-light irradiation at the end of 10 cycles. The FCN benefited from the absorption of solar energy and a large number of active sites. These advantages facilitated the efficient separation of photoexcited electron-hole pairs to hinder charge recombination. This work generates new insights into the preparation of highly effective FCN photocatalysts that may be put to various applications, especially in the fields of energy and environment.

Interfacial solar water evaporation has emerged as an effective technique for converting solar energy to thermal energy, which can then be applied to clean water production and sewage treatment. This review discusses the primary characterization techniques used to evaluate the key aspects of interfacial solar water evaporators: the intrinsic and performance evaluation. Each technique is discussed with a brief explanation of its foundations, followed by carefully selected examples. This review is aimed at assisting materials chemists and physicists, particularly students, in choosing the most appropriate techniques for characterizing photothermal materials.

An effective strategy for significantly enhancing photocatalytic activity of composite materials is to construct heterojunctions. Herein, a series of imidazole-modified heterostructured g-C₃N₄/SnO (CNIS) Z-scheme photocatalysts were prepared by calcination methods, leading to superior photocatalytic performance than pure SnO and imidazole-modified g-C₃N₄. Rhodamine B (Rh B) aqueous solution was taken as the target pollutant, and the result presented that both imidazole modification and the Z-scheme heterojunction construction benefited from significant enhancement in photocatalytic activity. Moreover, it is revealed that electrons were transferred from imidazole-modified g-C₃N₄ to SnO through the interface of the composite by XPS analysis. Under visible light (>420 nm) irradiation, the built-in electric field, band edge bending, and Coulomb interaction work synergistically to drive the recombination of relatively useless electrons and holes in the hybrid. As a result, the residual electrons and holes, which possess enhanced reducibility and oxidizability, endow the composite with exceptional redox capability. This research can not only deepen our comprehension of designing and fabricating innovative Z-scheme heterojunction photocatalysts but also presents an effective approach to tackle environmental pollution issues in the future.