Electrochemical water splitting is a promising method for generating green hydrogen gas, offering a sustainable approach to addressing global energy challenges. However, the sluggish kinetics of the anodic oxygen evolution reaction (OER) poses a great obstacle to its practical application. Recently, increasing attention has been focused on introducing various external stimuli to modify the OER process.
View Article and Find Full Text PDFSorting recyclable trash is critical to reducing energy consumption and mitigating environmental pollution. Currently, trash sorting heavily relies on manpower. Computer vision technology enables automated trash sorting.
View Article and Find Full Text PDFEndoplasmic reticulum stress (ERS) and oxidative stress (OS) are adaptive responses of the body to stressor stimulation. Although it has been verified that Trichinella spiralis (T. spiralis) can induce ERS and OS in the host, their association is still unclear.
View Article and Find Full Text PDFCobalt oxyhydroxide (CoOOH) is a promising catalytic material for oxygen evolution reaction (OER). In the traditional CoOOH structure, Co exhibits a low-spin state configuration ([Formula: see text]), with electron transfer occurring in face-to-face [Formula: see text] orbitals. In this work, we report the successful synthesis of high-spin state Co CoOOH structure, by introducing coordinatively unsaturated Co atoms.
View Article and Find Full Text PDFA coupled oxygen evolution mechanism (COM) during oxygen evolution reaction (OER) has been reported in nickel oxyhydroxides (NiOOH)-based materials by realizing e band (3d electron states with e symmetry) broadening and light irradiation. However, the link between the e band broadening extent and COM-based OER activities remains unclear. Here, NiFeOOH (x = 0, 0.
View Article and Find Full Text PDFPorous carbon materials with hollow structure, on account of the extraordinary morphology, reveal fascinating prospects in lithium-ion batteries, electrocatalysis, etc. However, collapse in ultrathin carbon spheres due to insufficient rigidity in such thin materials obstructs further enhanced capability. Based on hyper-crosslinked polymers (HCPs) with sufficient pore structure and rigid framework, a new bottom-up strategy is proposed to construct SiO @HCPs directly from aromatic monomers.
View Article and Find Full Text PDFAn acidification-assisted assembly strategy is presented for embedding activated carbon nanospheres into polymer-derived porous carbon networks to form a carbon heterostructure with an ultrahigh surface area of 2042 m g. The heterostructure, only containing elements of C and O, exhibits remarkably enhanced oxygen reduction activity, comparable to that of commercial Pt/C.
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