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As a low‐cost alternative to noble metals, Cu plays an important role in industrial catalysis, such as water‐gas shift reaction, methanol or ethanol oxidation, hydrogenation of oils, CO oxidation, among many others. An important step in optimizing Cu catalyst performance is control of nanoparticles size, distribution, and the interface with the support. While proton conducting perovskites can enhance the metal catalytic activity when acting as the support, there has been limited investigation of in situ growth of Cu metal nanoparticles from the proton conductors and its catalytic performance. Here, Cu nanoparticles are tracked exsolved from an A‐site‐deficient proton‐conducting barium cerate‐zirconate using scanning electron microscopy, revealing a continuous phase change during exsolution as a function of reduction temperature. Combined with the phase diagram and cell parameter change during reduction, a new exsolution mechanism is proposed for the first time which provides insight into tailoring metal particles interfaces at proton conducting oxide surfaces. Furthermore, the catalytic behavior in the CO oxidation reaction is explored and, it is observed that these new nanostructures can rival state of the art catalysts over long term operation. [ABSTRACT FROM AUTHOR]

High‐performance nanoparticle platforms can drive catalysis progress to new horizons, delivering environmental and energy targets. Nanoparticle exsolution offers unprecedented opportunities that are limited by current demanding process conditions. Unraveling new exsolution pathways, particularly at low‐temperatures, represents an important milestone that will enable improved sustainable synthetic route, more control of catalysis microstructure as well as new application opportunities. Herein it is demonstrated that plasma direct exsolution at room temperature represents just such a step change in the synthesis. Moreover, the factors that most affect the exsolution process are identified. It is shown that the surface defects produced initiate exsolution under a brief ion bombardment of an argon low‐pressure and low‐temperature plasma. This results in controlled nanoparticles with diameters ≈19–22 nm with very high number densities thus creating a highly active catalytic material for CO oxidation which rivals traditionally created exsolved samples. [ABSTRACT FROM AUTHOR]

Supported bimetallic nanoparticles used for various chemical transformations appear to be more appealing than their monometallic counterparts, because of their unique properties mainly originating from the synergistic effects between the two different metals. Exsolution, a relatively new preparation method for supported nanoparticles, has earned increasing attention for bimetallic systems in the past decade, not only due to the high stability of the resulting nanoparticles but also for the potential to control key particle properties (size, composition, structure, morphology, etc.). In this review, we summarize the trends and advances on exsolution of bimetallic systems and provide prospects for future studies in this field. [ABSTRACT FROM AUTHOR]

Particles dispersed on the surface of oxide supports have enabled a wealth of applications in electrocatalysis, photocatalysis, and heterogeneous catalysis. Dispersing nanoparticles within the bulk of oxides is, however, synthetically much more challenging and therefore less explored, but could open new dimensions to control material properties analogous to substitutional doping of ions in crystal lattices. Here we demonstrate such a concept allowing extensive, controlled growth of metallic nanoparticles, at nanoscale proximity, within a perovskite oxide lattice as well as on its surface. By employing operando techniques, we show that in the emergent nanostructure, the endogenous nanoparticles and the perovskite lattice become reciprocally strained and seamlessly connected, enabling enhanced oxygen exchange. Additionally, even deeply embedded nanoparticles can reversibly exchange oxygen with a methane stream, driving its redox conversion to syngas with remarkable selectivity and long term cyclability while surface particles are present. These results not only exemplify the means to create extensive, self‐strained nanoarchitectures with enhanced oxygen transport and storage capabilities, but also demonstrate that deeply submerged, redox‐active nanoparticles could be entirely accessible to reaction environments, driving redox transformations and thus offering intriguing new alternatives to design materials underpinning several energy conversion technologies. [ABSTRACT FROM AUTHOR]

Limestones exposed north of Raub, Pahang, Malaysia, and sandwiched between the Bentong-Raub Suture Zone and the westernmost margin of the Sukhothai Arc terrane, yield a late Dienerian (late Induan) conodont fauna. The co-occurrence of Neospathodus dieneri Sweet (morphotypes 1, 2 and 3) and Neospathodus pakistanensis Sweet represents the Neospathodus dieneri morphotype 3 sub-zone of the Neospathodus dieneri Zone. The sampled limestones are interpreted as the northwards extension of the Jerus Limestone which crops out near Cheroh and Jerus villages, significantly extending the known outcrop of the Jerus Limestone northwards. The Jerus Limestone is interpreted as hemipelagic and formed in a foredeep or forearc setting on top of the accretionary complex formed by eastwards subduction of the Palaeo-Tethys during the Lower to Middle Triassic. [ABSTRACT FROM AUTHOR]

Bimetallic exsolution, catalysis, electrochemistry, energy conversion, nanomaterials In the Minireview on page 6666, C. Tang, K. Kousi, D. Neagu, and I. S. Metcalfe review the, approximately, 70 studies published so far, on bimetallic exsolution and identified research trends in this area. Keywords: bimetallic exsolution; catalysis; electrochemistry; energy conversion; nanomaterials EN bimetallic exsolution catalysis electrochemistry energy conversion nanomaterials 1 1 1 04/19/21 20210416 NES 210416 B Exsolution is a relatively new research hotspot b which can be traced back to 2002. [Extracted from the article]