Wentao Yuan

High-performance hydrogen evolution electrocatalysis by layer-controlled MoS2 nanosheets

Hydrogen is considered as an important clean energy carrier for the future, and electrocatalytic splitting of water is one of the most efficient technologies for hydrogen production. As a potential alternative to Pt-based catalysts in hydrogen evolution reaction (HER), two-dimensional (2D) molybdenum sulfide (MoS2) nanomaterials have attracted enormous research interest, while the structure control for high-performance HER electrocatalysis remains a considerable challenge due to the lack of efficient preparation techniques. Herein, we reported a one-pot chemical method to directly synthesize 2D MoS2 with controllable layers. Multiple-layer MoS2 (ML-MoS2), few-layer MoS2 (FL-MoS2) and single-layer MoS2 coating on carbon nanotubes (SL-MoS2-CNTs) can be efficiently prepared through the modulation of experimental conditions. The enhanced catalytic activity in HER is demonstrated by reducing the layer number of MoS2 nanosheets. Remarkably, the optimized SL-MoS2-CNTs sample showed long-term durability with an accelerated degradation experiment even after more than 10 000 recycles, and high HER activity with an onset overpotential of only ∼40 mV vs. RHE. This study introduces a novel, cheap and facile strategy to prepare layer-controlled 2D MoS2 nanosheets in a large quantity, and is expected to broaden the already wide range energy applications of 2D MoS2 nanosheets.

Real-Time Observation of Reconstruction Dynamics on TiO2(001) Surface under Oxygen via an Environmental Transmission Electron Microscope

The surface atomic structure has a remarkable impact on the physical and chemical properties of metal oxides and has been studied extensively by scanning tunneling microscopy. However, acquiring real-time information on the formation and evolution of the surface structure remains a great challenge. Here we use environmental transmission electron microscopy to directly observe the stress-induced reconstruction dynamics on the (001) surface of anatase TiO2. Our in situ results unravel for the first time how the (1 × 4) reconstruction forms and how the metastable (1 × 3) and (1 × 5) patterns transform into the (1 × 4) surface stable structure. With the support of first-principles calculations, we find that the surface evolution is driven by both low coordinated atoms and surface stress. This work provides a complete picture of the structural evolution of TiO2(001) under oxygen atmosphere and paves the way for future studies of the reconstruction dynamics of other solid surfaces.

Atomic-Scale Observation of Vapor–Solid Nanowire Growth via Oscillatory Mass Transport

In situ atomic-scale transmission electron microscopy (TEM) can provide critical information regarding growth dynamics and kinetics of nanowires. A catalyst-aided nanowire growth mechanism has been well-demonstrated by this method. By contrast, the growth mechanism of nanowires without catalyst remains elusive because of a lack of crucial information on related growth dynamics at the atomic level. Herein, we present a real-time atomic-scale observation of the growth of tungsten oxide nanowires through an environmental TEM. Our results unambiguously demonstrate that the vapor-solid mechanism dominates the nanowire growth, and the oscillatory mass transport on the nanowire tip maintains the noncatalytic growth. Autocorrelation analysis indicates that adjacent nucleation events in the nanowire growth are independent of each other. These findings may improve the understanding of the vapor-solid growth mechanism of nanowires.

Direct observation of Pt nanocrystal coalescence induced by electron-excitation-enhanced van der Waals interactions

AbstractNanocrystal coalescence has attracted paramount attention in nanostructure fabrication in the past decades. Tremendous endeavor and progress have been made in understanding its mechanisms, benefiting from the development of transmission electron microscopy. However, many mechanisms still remain unclear, especially for nanocrystals that lack a permanent dipole moment standing on a solid substrate. Here, we report an in situ coalescence of Pt nanocrystals on an amorphous carbon substrate induced by electron-excitationenhanced van der Waals interactions studied by transmission electron microscopy and first principles calculations. It is found that the electron-beam-induced excitation can significantly enhance the van der Waals interaction between Pt nanocrystals and reduce the binding energy between Pt nanocrystals and the carbon substrate, both of which promote the coalescence. This work extends our understanding of the nanocrystal coalescence observed in a transmission electron microscope and sheds light on a potential pathway toward practical electronbeam-controlled nanofabrication.

In situ TEM observation of dissolution and regrowth dynamics of MoO2 nanowires under oxygen

Direct observation of the dissolution behavior of nanomaterials could provide fundamental insight to understanding their anisotropic properties and stability. The dissolution mechanism in solution and vacuum has been well documented. However, the gas-involved dissolution and regrowth have seldom been explored and the mechanisms remain elusive. We report herein, an in situ TEM study of the dissolution and regrowth dynamics of MoO2 nanowires under oxygen using environmental transmission electron microscopy (ETEM). For the first time, oscillatory dissolution on the nanowire tip is revealed, and, intriguingly, simultaneous layer-by-layer regrowth on the sidewall facets is observed, leading to a shorter and wider nanowire. Combined with first-principles calculations, we found that electron beam irradiation caused oxygen loss in the tip facets, which resulted in changing the preferential growth facets and drove the morphology reshaping.

Recent advances in gas-involved in situ studies via transmission electron microscopy

Gases that are widely used in research and industry have a significant effect on both the configuration of solid materials and the evolution of reactive systems. Traditional studies on gas–solid interactions have mostly been static and post-mortem and unsatisfactory for elucidating the real active states during the reactions. Recent developments of controlled-atmosphere transmission electron microscopy (TEM) have led to impressive progress towards the simulation of real-world reaction environments, allowing the atomic-scale recording of dynamic events. In this review, on the basis of the in situ research of our group, we outline the principles and features of the controlled-atmosphere TEM techniques and summarize the significant recent progress in the research activities on gas–solid interactions, including nanowire growth, catalysis, and metal failure. Additionally, the challenges and opportunities in the real-time observations on such platform are discussed.

Controllable synthesis of rutile titania with novel curved surfaces

We report a facile organic-free hydrothermal strategy to fabricate rutile TiO2 single crystals with a new type of curved surfaces which consist of high-energy-facet-bound nanohills rather than quasi-continuous miller-index microfacets. Moreover, by solely altering the concentration of F−, the proportion of facets as well as the aspect ratio of TiO2 could be readily controlled.

A Rational Solid-State Synthesis of Supported Au–Ni Bimetallic Nanoparticles with Enhanced Activity for Gas-Phase Selective Oxidation of Alcohols

A facile confined solid-state seed-mediated alloying strategy is applied for the rational synthesis of supported Au-Ni bimetallic nanoparticles (BMNPs). The method sequentially deposits nickel salts and AuNP seeds into the ordered array of extra-large mesopores (EP-FDU-12 support) followed by a high-temperature annealing process. The size, structure, and composition of the AuNi BMNPs can be well tuned by varying the AuNP seeds, annealing temperature, and feeding ratio of metal precursors. Kinetic studies and DFT calculations suggest that the introduction of the Ni component can significantly prompt the O2 activation on AuNPs, which is critical for the selective alcohol oxidation using molecular O2 as the oxidant. The optimal Au-Ni BMNP catalyst showed the highest turnover frequency (TOF) (59 000 h-1, 240 °C) and highest space-time yield (STY) of benzyl aldehyde (BAD) productivity (9.23 kg·gAu-1·h-1) in the gas-phase oxidation of benzyl alcohol (BA), which is at least about 5-fold higher than that of other supported Au catalysts.