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Localized surface plasmon resonances (LSPR) in near-infrared (NIR) region have been extensively studied for copper chalcogenide nanostructures, not only for the absorption enhancement but also tunable LSPR characteristics with their free carrier concentrations or defects. In the present work, one-step cation exchange method has been used to synthesize Cu2−xS nanowires with x varied between 0 and 1, including Cu2S, Cu7S4 and CuS and so forth. The plasmonic band of Cu2−xS nanowires shifts to a shorter wavelength with the increase in x, as observed in vis-NIR spectra, which is attributed to the increase in density of copper vacancies. The Cu2−xS nanowires have been used as catalysts towards the photocatalytic generation of H2 from ammonia borane (AB). Among samples with different Cu-S compositions, Cu7S4 samples exhibited the highest activity in terms of H2 evolution rate (25.54 mmol/g h). Moreover, a marked enhancement of the H2 evolution rate (157.04 mmol/g h) could be achieved after decorating the Cu2−xS nanowires with Pd nanoparticles to form the hybrid structures. The results of the present investigation may lead to an effective strategy for the design and development of LSPR materials for photocatalytic applications.

Hydrogen spillover, the simultaneous diffusion of protons (H+) and electrons (e−) is considered to be applicable to ubiquitous technologies related to hydrogen but limited to over reducible metal oxides. The present work demonstrates that a non-reducible MgO with heteroatom Al dopants (Al–MgO) allows hydrogen spillover in the same way as reducible metal oxides. Furthermore, a H+ storage capacity of this material owing to hydrogen spillover is more than three times greater than those of various standard metal oxides based on H+ transport channels within its bulk region. Atomic hydrogen diffuses over the non-reducible Al–MgO produces active H+-e− pairs, as also occurs on reducible metal oxides, to enhance the catalytic performance of Ni during CO2 hydrogenation. The H+ and e− diffusion pathways generated by the heteroatom Al doping are disentangled based on systematic characterizations and calculations. This work provides a new strategy for designing functional materials intended to hydrogen spillover for diverse applications in a future hydrogen-based society. Hydrogen spillover is typically associated with reducible metal oxides and considered relevant for various hydrogen-related technologies. Here, the authors demonstrate that a non-reducible MgO doped with heteroatom Al enables hydrogen spillover similarly to reducible metal oxides. [ABSTRACT FROM AUTHOR]

Metal 3D printing is revolutionizing the industry by enabling rapid and cost‐effective production of complex metal 3D products with intricate geometries, attracting significant attention in recent years. Particularly, metal 3D‐printed catalysts have emerged as a cutting‐edge fusion technology that serves as both catalysts and reactors, referred to as self‐catalytic reactors (SCRs). Therefore, this concept article aims to introduce the recent advancements in metal 3D printing technology in the catalyst and reactor field, and illustrate the various aspects for the rational design of self‐catalytic reactors. [ABSTRACT FROM AUTHOR]