Explore the vast range of titles available.

The recent availability of shale gas has led to a renewed interest in C-H bond activation as the first step towards the synthesis of fuels and fine chemicals. Heterogeneous catalysts based on Ni and Pt can perform this chemistry, but deactivate easily due to coke formation. Cu-based catalysts are not practical due to high C-H activation barriers, but their weaker binding to adsorbates offers resilience to coking. Using Pt/Cu single-atom alloys (SAAs), we examine C-H activation in a number of systems including methyl groups, methane and butane using a combination of simulations, surface science and catalysis studies. We find that Pt/Cu SAAs activate C-H bonds more efficiently than Cu, are stable for days under realistic operating conditions, and avoid the problem of coking typically encountered with Pt. Pt/Cu SAAs therefore offer a new approach to coke-resistant C-H activation chemistry, with the added economic benefit that the precious metal is diluted at the atomic limit.

We present a combination of experiments and theory to study the effect of sulfur doping in hard carbons anodes for sodium-ion batteries. Hard carbons are synthesised through a two step process: hydrothermal carbonisation followed by pyrolysis of a biomass-derived carbon precursor. Subsequent sulfur doping is introduced via chemical-vapour deposition. The resulting sulfur-doped hard carbon shows enhanced sodium storage capacity with respect to the pristine material, with significantly improved cycling reversibility. Atomistic first principles simulations give insight into this behaviour, revealing that sulfur chemisorbed onto the hard carbon increases the sodium adsorption energies and facilitates sodium desorption. This mechanism would increase reversible Na storage, confirming our experimental observations and opening a pathway towards more efficient Na-ion batteries.

The conversion of oxygen-rich biomass into hydrocarbon fuels requires efficient hydrodeoxygenation catalysts during the upgrading process. However, traditionally prepared CoMoS 2 catalysts, although efficient for hydrodesulfurization, are not appropriate due to their poor activity, sulfur loss and rapid deactivation at elevated temperature. Here, we report the synthesis of MoS 2 monolayer sheets decorated with isolated Co atoms that bond covalently to sulfur vacancies on the basal planes that, when compared with conventionally prepared samples, exhibit superior activity, selectivity and stability for the hydrodeoxygenation of 4-methylphenol to toluene. This higher activity allows the reaction temperature to be reduced from the typically used 300 °C to 180 °C and thus allows the catalysis to proceed without sulfur loss and deactivation. Experimental analysis and density functional theory calculations reveal a large number of sites at the interface between the Co and Mo atoms on the MoS 2 basal surface and we ascribe the higher activity to the presence of sulfur vacancies that are created local to the observed Co–S–Mo interfacial sites. Converting oxygen-rich biomass into fuels requires the removal of oxygen groups through hydrodeoxygenation. MoS 2 monolayer sheets decorated with isolated Co atoms bound to sulfur vacancies in the basal plane have now been synthesized that exhibit superior catalytic activity, selectivity and stability for the hydrodeoxygenation of 4-methylphenol to toluene when compared to conventionally prepared materials.

Many industrial heterogeneous catalysts often use precious metals such as Pt and Pd thanks to their ability to catalyse a vast array of chemical reactions with exceptional activity. Unfortunately, the excellent reactivity of these metals results in poor selectivity, high susceptibility to poisoning and catalyst deactivation. One strategy that has been fruitful in overcoming these shortcomings is to alloy the catalytically active metals with those that are more selective, for example the coinage metals. A special class of these bimetallic surfaces may be formed by doping the inert host metal with a sufficiently low concentration of the catalytically active metal such that these dopant atoms isolate as individual, atomic dispersed ensembles in the surface layer of the host metal; such a material is known as a Single Atom Alloy (SAA). In this thesis, we use a dual-scale theoretical approach to develop a fundamental understanding of SAAs and their behaviour in catalytic systems. On the atomistic level, we make use of density functional theory (DFT) to investigate the electronic structure of SAAs, evaluating their thermodynamic stability and quantifying their surface interactions with various chemical species. Combining data acquired from DFT with kinetic Monte Carlo (KMC) simulation, we perform dynamic studies on length scales that are more relevant to real catalysis, allowing for the prediction of catalytic metrics. In particular, we show that the surface chemical heterogeneity of a SAAs results in novel catalytic properties, arising from combined weak adsorption and low activation energies for several bond dissociation reactions; that Pt/Cu SAAs can perform low temperature C-H bond without carbon deposition; and that SAAs offer strong resistivity to catalytic poisoning. Our findings will facilitate the discovery of new alloy catalysts that exhibit novel catalytic behaviour that can be fine-tuned in terms of activity, selectivity and stability.

The conversion of oxygen-rich biomass into hydrocarbon fuels requires efficient hydrodeoxygenation catalysts during the upgrading process. However, traditionally prepared CoMoS catalysts, although efficient for hydrodesulfurization, are not appropriate due to their poor activity, sulfur loss and rapid deactivation at elevated temperature. Here, we report the synthesis of MoS monolayer sheets decorated with isolated Co atoms that bond covalently to sulfur vacancies on the basal planes that, when compared with conventionally prepared samples, exhibit superior activity, selectivity and stability for the hydrodeoxygenation of 4-methylphenol to toluene. This higher activity allows the reaction temperature to be reduced from the typically used 300 °C to 180 °C and thus allows the catalysis to proceed without sulfur loss and deactivation. Experimental analysis and density functional theory calculations reveal a large number of sites at the interface between the Co and Mo atoms on the MoS basal surface and we ascribe the higher activity to the presence of sulfur vacancies that are created local to the observed Co-S-Mo interfacial sites.

Platinum step edges dominate electrocatalytic activity in fuel cells and electrolysers, yet their atomistic electrochemical behaviour remains poorly understood. Here, we employ ab initio molecular dynamics under controlled electrode potentials to model a realistic stepped Pt--water interface incorporating experimentally observed (111)\\(\\)(111) and (111)\\(\\)(100) edge motifs. This allows us to resolve, for the first time, the site-specific structure, charge distribution, and electrostatics of the electric double layer at a nanostructured Pt surface. We find that differential capacitance near the potential of zero charge (PZC) arises almost entirely from potential-dependent chemisorption of water on flat (111) terraces. In contrast, step edges are saturated with chemisorbed water even below the PZC and thus do not contribute to the capacitance. Instead, edges accumulate excess positive charge and exhibit a locally elevated electrostatic potential, as revealed by spatially resolved macroscopic potential profiles. This electrostatic asymmetry implies a greater barrier for electron accumulation at step sites compared to terraces, consistent with enhanced charge localisation and reactivity. Finally, the higher-in-energy d-band centre and sharper projected density of states at edge atoms further support their role as active, positively charged centres. Together, these results provide a mechanistic explanation for the observed experimental shift of the PZC with step density and establish a predictive framework for understanding and optimising interfacial charging in nanostructured Pt electrocatalysts.

The oxygen reduction reaction (ORR) in proton exchange membrane fuel cells plays an important role in the H2 economy. Pt-based alloy catalysts with tuned d-band centres are widely regarded as the most efficient catalysts. Here we report that the average size of Pt domains in a Pt-Pd alloy, described as the Pt-Pt coordination number (C.N.), may measure the coordination environment of Pt and its effect on the d-states, to serve as a key geometric descriptor for the ORR activity. The decrease of Pt-Pt C.N. from 10.8 in commercial Pt nanoparticles to 1.33 in Pt1Pd493 alloy leads to an exponential increase in the Pt mass activity from 0.18 to 4.86 A/mgPt. Density functional theory calculations show that low C.N. sites of Pt within the Pd host have low O-O dissociation barriers, favouring the four-electron dissociative pathway. The precise engineering of Pt-Pt C.N. in an alloy is critical for optimising metal use in the activation of chemically stable compounds, particularly in the context of catalysis for renewable energy.

Our perception of free will is composed of a desire to act (volition) and a sense of responsibility for our actions (agency). Brain damage can disrupt these processes, but which regions are most important for free will perception remains unclear. Here, we study focal brain lesions that disrupt volition, causing akinetic mutism (n = 28), or disrupt agency, causing alien limb syndrome (n = 50), to better localize these processes in the human brain. Lesion locations causing either syndrome were highly heterogeneous, occurring in a variety of different brain locations. We next used a recently validated technique termed lesion network mapping to determine whether these heterogeneous lesion locations localized to specific brain networks. Lesion locations causing akinetic mutism all fell within one network, defined by connectivity to the anterior cingulate cortex. Lesion locations causing alien limb fell within a separate network, defined by connectivity to the precuneus. Both findings were specific for these syndromes compared with brain lesions causing similar physical impairments but without disordered free will. Finally, our lesion-based localization matched network localization for brain stimulation locations that disrupt free will and neuroimaging abnormalities in patients with psychiatric disorders of free will without overt brain lesions. Collectively, our results demonstrate that lesions in different locations causing disordered volition and agency localize to unique brain networks, lending insight into the neuroanatomical substrate of free will perception.

Helminth-induced eosinophils accumulate around the parasite at the site of infection, or in parasite-damaged tissues well after the helminth has left the site. The role of helminth-elicited eosinophils in mediating parasite control is complex. While they may contribute to direct parasite-killing and tissue repair, their involvement in long-term immunopathogenesis is a concern. In allergic Siglec-F hi CD101 hi , eosinophils are associated with pathology. Research has not shown if equivalent subpopulations of eosinophils are a feature of helminth infection. In this study, we demonstrate that lung migration of rodent hookworm Nippostrongylus brasiliensis ( Nb ) results in a long-term expansion of distinct Siglec-F hi CD101 hi eosinophil subpopulations. Nb -elevated eosinophil populations in the bone marrow and circulation did not present this phenotype. Siglec-F hi CD101 hi lung eosinophils exhibited an activated morphology including nuclei hyper-segmentation and cytoplasm degranulation. Recruitment of ST2 + ILC2s and not CD4 + T cells to the lungs was associated with the expansion of Siglec-F hi CD101 hi eosinophils. This data identifies a morphologically distinct and persistent subset of Siglec-F hi CD101 hi lung eosinophils induced following Nb infection. These eosinophils may contribute to long-term pathology following helminth infection.

Background Early life microbiota is an important determinant of immune and metabolic development and may have lasting consequences. The maternal gut microbiota during pregnancy or breastfeeding is important for defining infant gut microbiota. We hypothesized that maternal gut microbiota during pregnancy and breastfeeding is a critical determinant of infant immunity. To test this, pregnant BALB/c dams were fed vancomycin for 5 days prior to delivery (gestation; Mg), 14 days postpartum during nursing (Mn), or during gestation and nursing (Mgn), or no vancomycin (Mc). We analyzed adaptive immunity and gut microbiota in dams and pups at various times after delivery. Results In addition to direct alterations to maternal gut microbial composition, pup gut microbiota displayed lower α-diversity and distinct community clusters according to timing of maternal vancomycin. Vancomycin was undetectable in maternal and offspring sera, therefore the observed changes in the microbiota of stomach contents (as a proxy for breastmilk) and pup gut signify an indirect mechanism through which maternal intestinal microbiota influences extra-intestinal and neonatal commensal colonization. These effects on microbiota influenced both maternal and offspring immunity. Maternal immunity was altered, as demonstrated by significantly higher levels of both total IgG and IgM in Mgn and Mn breastmilk when compared to Mc. In pups, lymphocyte numbers in the spleens of Pg and Pn were significantly increased compared to Pc. This increase in cellularity was in part attributable to elevated numbers of both CD4+ T cells and B cells, most notable Follicular B cells. Conclusion Our results indicate that perturbations to maternal gut microbiota dictate neonatal adaptive immunity.