No abstract

Beyond the catalytic activity of nanocatalysts, the support with architectural design and explicit boundary could also promote the overall performance through improving the diffusion process, highlighting additional support for the morphology-dependent activity. To delineate this, herein, a novel mazelike-reactor framework, namely multi-voids mesoporous silica sphere (MVmSiO 2 ), is carved through a top-down approach by endowing core-shell porosity premade Stöber SiO 2 spheres. The precisely-engineered MVmSiO 2 with peripheral one-dimensional pores in the shell and interconnecting compartmented voids in the core region is simulated to prove combined hierarchical and structural superiority over its analogous counterparts. Supported with CuZn-based alloys, mazelike MVmSiO 2 nanoreactor experimentally demonstrated its expected workability in model gas-phase CO 2 hydrogenation reaction where enhanced CO 2 activity, good methanol yield, and more importantly, a prolonged stable performance are realized. While tuning the nanoreactor composition besides morphology optimization could further increase the catalytic performance, it is accentuated that the morphological architecture of support further boosts the reaction performance apart from comprehensive compositional optimization. In addition to the found morphological restraints and size-confinement effects imposed by MVmSiO 2 , active sites of catalysts are also investigated by exploring the size difference of the confined CuZn alloy nanoparticles in CO 2 hydrogenation employing both in-situ experimental characterizations and density functional theory calculations.

No abstract

Oxygen reduction reaction in a double perovskite material, PrBa 0.5 Sr 0.5 Co 1.5 Fe 0.5 O 5+δ (PBSCF), was studied for application as a cathode in a solid oxide fuel cell (SOFC). Electrochemical measurements were performed on a geometrically welldefined dense thin-film (0.8−2 μm thickness) electrode, fabricated as a symmetric cell. In combination with density functional theory (DFT) and molecular dynamics (MD) simulations, experiments provided an insight into the operating mechanism of the SOFC material tested at an open-circuit voltage. The dense thin-film electrode of PBSCF showed a thickness-dependent electrochemical performance, suggesting bulk diffusion limitation. To understand the origin of this diffusion-limiting electrochemical performance, DFT calculations were utilized to calculate the surface (γ) and oxygen vacancy formation (E OV ) energies. For example, E OV in the Pr plane (190 kJ/mol) of PBSCF was measured to be lower than that of the BaSr plane (E OV = 297 kJ/ mol). In addition, oxygen vacancies were difficult to be created in the BaSr/CoFe terminal surface (E OV = 341.6 kJ/mol) as compared to other terminal surfaces. MD simulations further elaborated on the nature of cation disordering in the surface and subsurface regions, consequently leading to the preferential segregation of the Ba cations to the surface, which is a known phenomenon in such double perovskite materials. Because of cation disordering and segregation of Ba species, the oxygen anion diffusivity (∼10 −12 cm 2 s −1 ), calculated from MD, in the near-surface region was observed to be 2 orders of magnitude lesser than that of the bulk (D = 2.98 × 10 −10 cm 2 s −1 ) of the material at 973 K. Surface characterization of the thin-film electrode using X-ray photoelectron spectroscopy was indicative of a nonperovskite Ba 2+ phase on the electrode surface. The segregation of Ba cations was linked with the transport of oxygen anions, which was limiting the electrochemical performance of the electrode.

No abstract

Metal promotion is the most widely adopted strategy for enhancing the hydrogenation functionality of an oxide catalyst. Typically, metal nanoparticles or dopants are located directly on the catalyst surface to create interfacial synergy with active sites on the oxide, but the enhancement effect may be compromised by insufficient hydrogen delivery to these sites. Here, we introduce a strategy to promote a ZnZrOx methanol synthesis catalyst by incorporating hydrogen activation and delivery functions through optimized integration of ZnZrOx and Pd supported on carbon nanotube (Pd/CNT). The CNT in the Pd/CNT + ZnZrOx system delivers hydrogen activated on Pd to a broad area on the ZnZrOx surface, with an enhancement factor of 10 compared to the conventional Pd-promoted ZnZrOx catalyst, which only transfers hydrogen to Pd-adjacent sites. In CO2 hydrogenation to methanol, Pd/CNT + ZnZrOx exhibits drastically boosted activity—the highest among reported ZnZrOx-based catalysts—and excellent stability over 600 h on stream test, showing potential for practical implementation.

No abstract

Mechanistic studies, utilizing molecular dynamics (MD) and density functional theory (DFT) calculations, were undertaken to provide a molecular level explanation of Ba cation segregation in double perovskite GdBaCo2O5+δ (GBCO) electrodes.