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A major challenge limiting the practical applications of nanomaterials is that the activities of nanostructures (NSs) increase with reduced size, often sacrificing their stability in the chemical environment. Under oxidative conditions, NSs with smaller sizes and higher defect densities are commonly expected to oxidize more easily, since high-concentration defects can facilitate oxidation by enhancing the reactivity with O2 and providing a fast channel for oxygen incorporation. Here, using FeO NSs as an example, we show to the contrary, that reducing the size of active NSs can drastically increase their oxidation resistance. A maximum oxidation resistance is found for FeO NSs with dimensions below 3.2 nm. Rather than being determined by the structure or electronic properties of active sites, the enhanced oxidation resistance originates from the size-dependent structural dynamics of FeO NSs in O2. We find this dynamic size effect to govern the chemical properties of active NSs.

The formation of solid electrolyte interphase (SEI) and lithium ion intercalation are two crucial processes in lithium ion batteries. Given the complexity and challenges involved in investigating real batteries, a combination of model batteries comprising well-defined ultrathin graphite electrodes with surface-sensitive techniques can provide valuable information on these processes. Here, a comparative study of the performance of batteries using regular- and high-concentration electrolytes (RCE and HCE) is presented, aided by a myriad of correlative surface science techniques. It is found that the SEI formed in HCE possesses a thinner organic layer and more inorganic substances. Such an effective SEI protects the graphite electrode and facilitates the processes of Li+ intercalation/deintercalation, thereby improving the reversibility and cycling stability of the battery, superior to those with RCE. Moreover, the battery performance can be readily tuned by switching the electrolytes. The good cycling stability of the battery can still be maintained in RCE after the preformation of a robust SEI on the ultrathin graphite electrode in HCE. This work highlights the importance of electrolyte-modulated SEI formation to battery performance and provides powerful platforms to comprehensively study the SEI formation and ion intercalation processes. [ABSTRACT FROM AUTHOR]

Supported metal catalysts are widely used for chemical conversion, in which construction of high density metal‐oxide or oxide‐metal interface is an important means to improve their reaction performance. Here, Cu@ZnOx encapsulation structure has been in situ constructed through gas‐phase migration of Zn species from ZnO particles onto surface of Cu nanoparticles under CO2 hydrogenation atmosphere at 450 °C. The gas‐phase deposition of Zn species onto the Cu surface and growth of ZnOx overlayer is self‐limited under the high temperature and redox gas (CO2/H2) conditions. Accordingly, high density ZnOx‐Cu interface sites can be effectively tailored to have an enhanced activity in CO2 hydrogenation to methanol. This work reveals a new route for the construction of active oxide‐metal interface and classic strong metal‐support interaction state through gas‐phase migration of support species induced by high temperature redox reaction atmosphere. [ABSTRACT FROM AUTHOR]

Surface and interface play critical roles in energy storage devices, calling for operando characterization techniques to probe the electrified surfaces/interfaces. In this work, surface science methodology, including electron spectroscopy and scanning probe microscopy, has been successfully applied to visualize electrochemical processes at operating electrode surfaces in an Al/graphite model battery. Intercalation of anions together with cations is directly observed in the surface region of a graphite electrode with tens of nanometers thickness, the concentration of which is one order higher than that in bulk. An intercalation pseudocapacitance mechanism and a double specific capacity in the electrode surface region are expected based on the super-dense intercalants and anion/cation co-intercalation, which are in sharp contrast to the battery-like mechanism in the electrode bulk. The distinct electrochemical mechanism at the electrode surface is verified by performance tests of real battery devices, showing that a surface-dominant, nanometer-thick graphite cathode outperforms a bulk-dominant, micrometer-thick graphite cathode. Our findings highlight the important surface effect of working electrodes in charge storage systems. [ABSTRACT FROM AUTHOR]

The self-assembled structure of submonolayer manganese phthalocyanine (MnPc) on Pb(111) surface is investigated by using low-temperature scanning tunneling microscopy (STM). A 'holelike' superlattice, which is superimposed on the self-assembled nearly quadratic network, is observed. High resolution STM images reveal that there are two distinct azimuthal orientations of MnPc molecules. It is found that by taking the two different orientations the self-assembly can further be optimized energetically by maximizing intermolecular orbital overlapping. It is this intralayer energy minimization process that leads to the characteristic holelike superlattice. [ABSTRACT FROM AUTHOR]