Pt-based catalysts can be poisoned by the chlorine formed during the oxidation of multicomponent volatile organic compounds (VOCs) containing chlorinated VOCs. Improving the low-temperature chlorine resistance of catalysts is important for industrial applications, although it is yet challenging. We hereby demonstrate the essential catalytic roles of a bifunctional catalyst with an atomic-scale metal/oxide interface constructed by an intermetallic compound nanocrystal. Introducing trichloroethylene (TCE) exhibits a less negative effect on the catalytic activity of the bimetallic catalyst for o-xylene oxidation, and the partial deactivation caused by TCE addition is reversible, suggesting that the bimetallic, HCl-etched Pt3Sn­(E)/CeO2 catalyst possesses much stronger chlorine resistance than the conventional Pt/CeO2 catalyst. On the site-isolated Pt–Sn catalyst, the presence of aromatic hydrocarbon significantly inhibits the adsorption strength of TCE, resulting in excellent catalytic stability in the oxidation of the VOC mixture. Furthermore, the large amount of surface-adsorbed oxygen species generated on the electronegative Pt is highly effective for low-temperature C–Cl bond dissociation. The adjacent promoter (Sn–O) possesses the functionality of acid sites to provide sufficient protons for HCl formation over the bifunctional catalyst, which is considered critical to maintaining the reactivity of Pt by removing Cl and decreasing the polychlorinated byproducts.

Moiré fringe, originated from the beating of two sets of lattices, is a commonly observed phenomenon in physics, optics, and materials science. Recently, a new method of creating moiré fringe via scanning transmission electron microscopy (STEM) has been developed to image materials’ structures at a large field of view. Moreover, this method shows great advantages in studying atomic structures of beam sensitive materials by significantly reduced electron dose. Here, the development of the STEM moiré fringe (STEM‐MF) method is reviewed. The authors first introduce the theory of STEM‐MF and then discuss the advances of this technique in combination with geometric phase analysis, annular bright field imaging, energy dispersive X‐ray spectroscopy, and electron energy loss spectroscopy. Applications of STEM‐MF on strain, defects, 2D materials, and beam‐sensitive materials are further summarized. Finally, the authors′ perspectives on the future directions of STEM‐MF are presented.

Iridium (Ir) single-atom catalysts (SACs) exhibit the extraordinary advantage in oxygen evolution reaction (OER) owing to their unique electronic structure and maximized atom utilization. However, the further development meets the...

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Coupling growth mechanism with N* and H*.