Size-dependent activity of carbon dots for photocatalytic H2 generation in combination with a molecular Ni cocatalyst.

Carbon dots (CDs) are low-cost light-absorbers in photocatalytic multicomponent systems, but their wide size distribution has hampered rational design and the identification of the factors that lead to their best performance. To address this challenge, we report herein the use of gel filtration size exclusion chromatography to separate amorphous, graphitic, and graphitic N-doped CDs depending on their lateral size to study the effect of their size on photocatalytic H2 evolution with a DuBois-type Ni cocatalyst. Transmission electron microscopy and dynamic light scattering confirm the size-dependent separation of the CDs, whereas UV-vis and fluorescence spectroscopy of the more monodisperse fractions show a distinct response which computational modelling attributes to a complex interplay between CD size and optical properties. A size-dependent effect on the photocatalytic H2 evolution performance of the CDs in combination with a molecular Ni cocatalyst is demonstrated with a maximum activity at approximately 2-3 nm CD diameter. Overall, size separation leads to a two-fold increase in the specific photocatalytic activity for H2 evolution using the monodisperse CDs compared to the as synthesized polydisperse samples, highlighting the size-dependent effect on photocatalytic performance.

Modulating Structural and Electronic Properties of Rare Archimedean and Johnson-Type Mn Cages.

High-nuclearity Mn complexes have attracted significant scientific attention due to their fascinating magnetic properties and their relevance to bioinorganic systems and catalysis. In this work, we demonstrate how the strong binding characteristics of phosphonate ligands can be coupled with sterically hindered carboxylate groups to influence the symmetry of Mn coordination clusters. We describe the structure of two high-nuclearity Mn coordination cages, {Mn12} and {Mn15}, synthesized using this approach. These cages are structurally related to the truncated tetrahedral geometry and adopt rare topological features of Archimedean and Johnson-type solids. Their structural attributes distinctively influence their magnetic properties and electrocatalytic H2O oxidation characteristics.

Altering the nature of coupling by changing the oxidation state in a {Mn6} cage.

Polynuclear transition metal complexes have continuously attracted interest owing to their peculiar electronic and magnetic properties which are influenced by the symmetry and connectivity of the metal centres. Understanding the full electronic picture in such cases often becomes difficult owing to the presence of multiple bridges between metal centres. We have investigated the electronic structure of a {Mn6} cage complex using computational and experimental approaches with the aim to understand the coupling between the manganese centres. The nature of the various coupling pathways has been determined using a novel methodology that involves perturbing the system while retaining the symmetry and analysing the effect on the coupling strength due to the perturbation. Furthermore, we have investigated the magnetic properties of this complex in higher oxidation states which reveals a switch in the nature of coupling from antiferromagnetic to ferromagnetic in addition to stabilisation of intermediate spin states.

Aggregation induced emission (AIE) active 4-amino-1,8-naphthalimide-Tröger's base for the selective sensing of chemical explosives in competitive aqueous media.

The 4-amino-1,8-naphthalimide-Tröger's base fluorophore, TBNap-TPy, adorned with phenyl-terpyridine moiety was synthesised and assessed for its aggregation-induced emission (AIE) behaviour. TBNap-TPy was further employed as a fluorescent sensor for the discriminative sensing of π-electron-deficient nitroaromatic; the TBNap-TPy displaying the largest fluorescence quenching with high selectivity for picric acid, a harmful environmental pollutant widely used in the dye industries.

Computationally Driven Discovery of Layered Quinary Oxychalcogenides: Potential p-Type Transparent Conductors?

n-type transparent conductors (TCs) are key materials in the modern optoelectronics industry. Despite years of research, the development of a high-performance p-type TC has lagged far behind that of its n-type counterparts, delaying the advent of "transparent electronics"-based p-n junctions. Here, we propose the layered oxysulfide [Cu2S2][Sr3Sc2O5] as a structural motif for discovering p-type TCs. We have used density functional theory to screen 24 compositions based on this motif in terms of their thermodynamic and dynamic stability and their electronic structure, thus predicting two p-type TCs and eight other stable systems with semiconductor properties. Following our predictions, we have successfully synthesized our best candidate p-type TC, [Cu2S2][Ba3Sc2O5], which displays structural and optical properties that validate our computational models. It is expected that the design principles emanating from this analysis will move the field closer to the realization of a high figure-of-merit p-type TC.

"Turn-on" fluorescence sensing of volatile organic compounds using a 4-amino-1,8-naphthalimide Tröger's base functionalised triazine organic polymer.

The 4-amino-1,8-naphthalimide Tröger's base functionalized triazine covalent organic polymer TB-TZ-COP was synthesised and employed as a "turn-on" fluorescent and a colorimetric sensor for the discriminative sensing of volatile organic compounds; the TB-TZ-COP displaying the largest fluorescent enhancement and high sensitivity for 1,4-dioxane, a harmful environmental pollutant classified as a Group 2B carcinogen.

Quasiparticle GW Calculations on Lead-Free Hybrid Germanium Iodide Perovskite CH3NH3GeI3 for Photovoltaic Applications.

Lead-free organic-inorganic halide perovskites have gained much attention as nontoxic alternatives to CH3NH3PbI3 in next-generation solar cells. In this study, we have examined the geometric and electronic properties of methylammonium germanium iodide CH3NH3GeI3 using density functional theory. Identifying a suitable functional to accurately model the germanium halide perovskites is crucial to allow the theoretical investigation for tuning the optoelectronic properties. The performance of various functionals (PBE, PBE+D3, PBEsol, PBEsol+D3, HSE06, and HSE06+D3) has been evaluated for modelling the structure and properties. The calculation of electronic properties was further refined by using the quasiparticle GW method on the optimized geometries, and that has an excellent agreement with the experiment. We report from our GW calculations that the characteristic of the density of states for CH3NH3GeI3 resembles the density of states for CH3NH3PbI3 and the effective masses of the charge carriers of CH3NH3GeI3 are comparable to the effective masses of CH3NH3PbI3 as well as silicon used in commercially available solar cells.

Flexible Metal-Organic Frameworks for Light-Switchable CO2 Sorption Using an Auxiliary Ligand Strategy.

We report the synthesis and characterization of two photoactive metal-organic frameworks (MOFs), TCM-14 and TCM-15. The compounds were synthesized by incorporating 4,4'-azopyridine auxiliary ligands into pto-type scaffolds that are composed of dinuclear copper(II) "paddle-wheel"-based secondary building units and flexible, acetylene-extended, tritopic benzoate linkers. Room temperature CO2 sorption of the MOFs was studied, and UV-light irradiation is shown to result in reduced CO2 adsorption under static conditions. TCM-15 reveals a dynamic response leading to an instant desorption of up to 20% of CO2 upon incidence of UV light because of the occurrence of nonperiodic structural changes. Physicochemical and computational density functional theory studies were carried out to gain insight into the mechanism of the interaction of light with the frameworks.

Layered CeSO and LiCeSO Oxide Chalcogenides Obtained via Topotactic Oxidative and Reductive Transformations.

The chemical accessibility of the CeIV oxidation state enables redox chemistry to be performed on the naturally coinage-metal-deficient phases CeM1- xSO (M = Cu, Ag). A metastable black compound with the PbFCl structure type (space group P4/ nmm: a = 3.8396(1) Å, c = 6.607(4) Å, V = 97.40(6) Å3) and a composition approaching CeSO is obtained by deintercalation of Ag from CeAg0.8SO. High-resolution transmission electron microscopy reveals the presence of large defect-free regions in CeSO, but stacking faults are also evident which can be incorporated into a quantitative model to account for the severe peak anisotropy evident in all the high-resolution X-ray and neutron diffractograms of bulk CeSO samples; these suggest that a few percent of residual Ag remains. A straw-colored compound with the filled PbFCl (i.e., ZrSiCuAs- or HfCuSi2-type) structure (space group P4/ nmm: a = 3.98171(1) Å, c = 8.70913(5) Å, V = 138.075(1) Å3) and a composition close to LiCeSO, but with small amounts of residual Ag, is obtained by direct reductive lithiation of CeAg0.8SO or by insertion of Li into CeSO using chemical or electrochemical means. Computation of the band structure of pure, stoichiometric CeSO predicts it to be a Ce4+ compound with the 4f-states lying approximately 1 eV above the sulfide-dominated valence band maximum. Accordingly, the effective magnetic moment per Ce ion measured in the CeSO samples is much reduced from the value found for the Ce3+-containing LiCeSO, and the residual paramagnetism corresponds to the Ce3+ ions remaining due to the presence of residual Ag, which presumably reflects the difficulty of stabilizing Ce4+ in the presence of sulfide (S2-). Comparison of the behavior of CeCu0.8SO with that of CeAg0.8SO reveals much slower reaction kinetics associated with the Cu1- xS layers, and this enables intermediate CeCu1- xLi xSO phases to be isolated.

Defects in orthorhombic LaMnO3 - ionic versus electronic compensation.

The ionic and electronic conductivity of orthorhombic LaMnO3 can be modified by introducing lower valence dopants at both the La and Mn sites. Alkaline earth doped perovskites, such as LaMnO3, have a variety of applications in catalysis, for nitrogen storage and reduction, and oxidation of volatile organic compounds, and as the oxygen electrode in solid oxide fuel cells. Here, we investigate doping with the divalent alkaline earth metals Mg, Ca, Sr and Ba, and the charge compensation mechanism. The energies of formation of isolated defects and clustered pairs were investigated at both La and Mn sites to establish the most probable site at which they will be introduced. The charge compensation mechanism for the introduction of alkaline earth dopants was examined by considering both ionic (formation of an oxygen vacancy for every two alkaline earth dopants introduced) and electronic compensation (a hole localised at the Mn site for each dopant introduced). Larger cations (Ca, Sr and Ba) were found to have lower defect formation energies when introduced at the La site, while the smaller Mg defect had lower formation energies when introduced to the Mn site. For all defects introduced, electronic compensation for the defect was found to be more energetically favourable, which will result in improved electronic conductivity of the material.

Synthesis, structural characterisation and antiproliferative activity of a new fluorescent 4-amino-1,8-naphthalimide Tröger's base-Ru(ii)-curcumin organometallic conjugate.

The synthesis, photophysics and biological investigation of fluorescent 4-amino-1,8-naphthalimide Tröger's bases (TB-1-TB-3) and a new Tröger's base p-cymene-Ru(ii)-curcumin organometallic conjugate (TB-Ru-Cur) are described; these compounds showed fast cellular uptake and displayed good luminescence and cytotoxicity against cervical cancer cells.

Modelling oxygen defects in orthorhombic LaMnO3 and its low index surfaces.

LaMnO3-based perovskites, which have been extensively studied as cathodes for high temperature solid oxide fuel cells (SOFCs), are also of interest for intermediate temperature SOFCs (T = 600-1000 K). Oxygen vacancy formation is required in LaMnO3 for oxygen diffusion, therefore a low vacancy formation energy is preferable. The stability of the low index surfaces of orthorhombic LaMnO3 has been investigated, with the {010} surface found to be the most stable. Surface stability was found to be affected by the La and Mn coordination, and the Mn-O bonds cleaved on surface formation. The crystal morphology has been predicted, in order to determine the most likely terminations to be present. The formation of oxygen vacancies in bulk LaMnO3 and at all of its low index surfaces has been examined, and it has been found that formation of vacancies in the bulk has a high energy, while there is a large variation in formation energies at the low index surfaces, which is likely to lead to segregation of vacancies to the surface of orthorhombic LaMnO3.

Methadone for cancer pain.

BACKGROUND: This is an updated review originally published in 2004 and first updated in 2007. This version includes substantial changes to bring it in line with current methodological requirements. Methadone is a synthetic opioid that presents some challenges in dose titration and is recognised to cause potentially fatal arrhythmias in some patients. It does have a place in therapy for people who cannot tolerate other opioids but should be initiated only by experienced practitioners. This review is one of a suite of reviews on opioids for cancer pain. OBJECTIVES: To determine the effectiveness and tolerability of methadone as an analgesic in adults and children with cancer pain. SEARCH METHODS: For this update we searched CENTRAL, MEDLINE, Embase, CINAHL, and clinicaltrials.gov, to May 2016, without language restriction. We also checked reference lists in relevant articles. SELECTION CRITERIA: We sought randomised controlled trials comparing methadone (any formulation and by any route) with active or placebo comparators in people with cancer pain. DATA COLLECTION AND ANALYSIS: All authors agreed on studies for inclusion. We retrieved full texts whenever there was any uncertainty about eligibility. One review author extracted data, which were checked by another review author. There were insufficient comparable data for meta-analysis. We extracted information on the effect of methadone on pain intensity or pain relief, the number or proportion of participants with 'no worse than mild pain'. We looked for data on withdrawal and adverse events. We looked specifically for information about adverse events relating to appetite, thirst, and somnolence. We assessed the evidence using GRADE and created a 'Summary of findings' table. MAIN RESULTS: We revisited decisions made in the earlier version of this review and excluded five studies that were previously included. We identified one new study for this update. This review includes six studies with 388 participants. We did not identify any studies in children.The included studies differed so much in their methods and comparisons that no synthesis of results was feasible. Only one study (103 participants) specifically reported the number of participants with a given level of pain relief, in this case a reduction of at least 20% - similar in both the methadone and morphine groups. Using an outcome of 'no worse than mild pain', methadone was similar to morphine in effectiveness, and most participants who could tolerate methadone achieved 'no worse than mild pain'. Adverse event withdrawals with methadone were uncommon (12/202) and similar in other groups. Deaths were uncommon except in one study where the majority of participants died, irrespective of treatment group. For specific adverse events, somnolence was more common with methadone than with morphine, while dry mouth was more common with morphine than with methadone. None of the studies reported effects on appetite.We judged the quality of evidence to be low, downgraded due to risk of bias and sparse data. For specific adverse events, we considered the quality of evidence to be very low, downgraded due to risk of bias, sparse data, and indirectness, as surrogates for appetite, thirst and somnolence were used.There were no data on the use of methadone in children. AUTHORS' CONCLUSIONS: Based on low-quality evidence, methadone is a drug that has similar analgesic benefits to morphine and has a role in the management of cancer pain in adults. Other opioids such as morphine and fentanyl are easier to manage but may be more expensive than methadone in many economies.

Correlating Lithium Hydroxyl Accumulation with Capacity Retention in V2O5 Aerogel Cathodes.

V2O5 aerogels are capable of reversibly intercalating more than 5 Li(+)/V2O5 but suffer from lifetime issues due to their poor capacity retention upon cycling. We employed a range of material characterization and electrochemical techniques along with atomic pair distribution function, X-ray photoelectron spectroscopy, and density functional theory to determine the origin of the capacity fading in V2O5 aerogel cathodes. In addition to the expected vanadium redox due to intercalation, we observed LiOH species that formed upon discharge and were only partially removed after charging, resulting in an accumulation of electrochemically inactive LiOH over each cycle. Our results indicate that the tightly bound water that is necessary for maintaining the aerogel structure is also inherently responsible for the capacity fade.

Modelling potential photovoltaic absorbers Cu3MCh4(M = V, Nb, Ta; Ch = S, Se, Te) using density functional theory.

The geometric and electronic properties of a series of potential photovoltaic materials, the sulvanite structured Cu3MCh4(M = V, Nb, Ta; Ch = S, Se, Te), have been computationally examined using both PBEsol+U and HSE06 methods to assess the materials' suitability for solar cell application and to compare the predictions of the two theoretical approaches. The lattice parameters, electronic density of states, and band gaps of the compounds have been calculated to ascertain the experimental agreement obtained by each method and to determine if any of the systems have an optical band gap appropriate for photovoltaic absorber materials. The PBEsol+U results are shown to achieve better agreement with experiment than HSE06 in terms of both lattice constants and band gaps, demonstrating that higher level theoretical methods do not automatically result in a greater level of accuracy than their computationally less expensive counterparts. The PBEsol+U calculated optical band gaps of five materials suggest potential suitability as photovoltaic absorbers, with values of 1.72 eV, 1.49 eV, 1.19 eV, 1.46 eV, and 1.69 eV for Cu3VS4, Cu3VSe4, Cu3VTe4, Cu3NbTe4, and Cu3TaTe4, respectively, although it should be noted that all fundamental band gaps are indirect in nature, which could lower the open-circuit voltage and hence the efficiency of prospective devices.

Using a cluster randomized controlled trial to determine the effects of intervention of battery and hardwired smoke alarms in New South Wales, Australia: Home fire safety checks pilot program.

INTRODUCTION: In 2014, Fire & Rescue New South Wales piloted the delivery of its home fire safety checks program (HFSC) aimed at engaging and educating targeted top "at risk" groups to prevent and prepare for fire. This pilot study aimed to assess the effectiveness of smoke alarms using a cluster randomized controlled trial. METHODS: Survey questionnaires were distributed to the households that had participated in the HFSC program (intervention group). A separate survey questionnaire was distributed to the control group that was identified with similar characteristics to the intervention group in the same suburb. To adjust for potential clustering effects, generalized estimation equations with a log link were used. RESULTS: Multivariable analyses revealed that battery and hardwired smoking alarm usage increased by 9% and 3% respectively among the intervention group compared to the control group. Females were more likely to install battery smoke alarms than males. Respondents who possessed a certificate or diploma (AOR=1.31, 95% CI 1.00-1.70, P=0.047) and those who were educated up to years 8-12 (AOR=1.32, 95% CI 1.06-1.64, P=0.012) were significantly more likely to install battery smoke alarms than those who completed bachelor degrees. Conversely, holders of a certificate or diploma and people who were educated up to years 8-12 were 31% (AOR=0.69, 95% CI 0.52-0.93, P=0.014) and 24% (AOR=0.76, 95% CI 0.60-0.95, P=0.015) significantly less likely to install a hardwired smoke alarm compared to those who completed bachelor degrees. CONCLUSIONS: This pilot study provided evidence of the benefit of the HFSC in New South Wales. PRACTICAL APPLICATIONS: Fire safety intervention programs, like HFSC, need to be targeted to male adults with lower level of schooling even when they are aware of their risks.

Assessing the potential of Mg-doped Cr2O3 as a novel p-type transparent conducting oxide.

One of the current challenges faced by material scientists is the development of a p-type transparent conducting oxide with levels of optical transparency and electronic conductivity to equal those of the universally n-type industry leaders such as Sn-doped In2O3. The discovery of a p-type analogue would allow for the combination of both polarities into a heterojunction, accessing the potential for transparent electronics. In this study, an insulating material, Cr2O3, is investigated both experimentally and computationally to determine if it is a viable p-type host matrix as has been recently proposed in the literature. The geometric and electronic structure are examined by high resolution x-ray diffraction, x-ray photoelectron spectroscopy, and periodic density functional theory (specifically, PBE + U). By incorporating Mg and performing a comprehensive defect analysis, the dominant intrinsic and extrinsic carriers in the material are determined, and it is shown that Cr2O3 has the potential to display p-type conductivity when appropriately doped.

Occupation matrix control of d- and f-electron localisations using DFT + U.

The use of a density functional theory methodology with on-site corrections (DFT + U) has been repeatedly shown to give an improved description of localised d and f states over those predicted with a standard DFT approach. However, the localisation of electrons also carries with it the problem of metastability, due to the possible occupation of different orbitals and different locations. This study details the use of an occupation matrix control methodology for simulating localised d and f states with a plane-wave DFT + U approach which allows the user to control both the site and orbital localisation. This approach is tested for orbital occupation using octahedral and tetrahedral Ti(iii) and Ce(iii) carbonyl clusters and for orbital and site location using the periodic systems anatase-TiO2 and CeO2. The periodic cells are tested by the addition of an electron and through the formation of a neutral oxygen vacancy (leaving two electrons to localise). These test systems allow the successful study of orbital degeneracies, the presence of metastable states and the importance of controlling the site of localisation within the cell, and it highlights the use an occupation matrix control methodology can have in electronic structure calculations.

Ceria co-doping: synergistic or average effect?

Ceria (CeO2) co-doping has been suggested as a means to achieve ionic conductivities that are significantly higher than those in singly doped systems. Rekindled interest in this topic over the last decade has given rise to claims of much improved performance. The present study makes use of computer simulations to investigate the bulk ionic conductivity of rare earth (RE) doped ceria, where RE = Sc, Gd, Sm, Nd and La. The results from the singly doped systems are compared to those from ceria co-doped with Nd/Sm and Sc/La. The pattern that emerges from the conductivity data is consistent with the dominance of local lattice strains from individual defects, rather than the synergistic co-doping effect reported recently, and as a result, no enhancement in the conductivity of co-doped samples is observed.

Cu3MCh3 (M = Sb, Bi; Ch = S, Se) as candidate solar cell absorbers: insights from theory.

As the thin film photovoltaic sector continues to expand, there is an emerging need to base these technologies on abundant, low cost materials in place of the expensive, rare, or toxic elements such as Te, In, or Cd that currently constitute the industry standards. To this end, the geometric and electronic structure of four materials comprising low cost, earth abundant elements (Cu3SbS3, Cu3SbSe3, Cu3BiS3, and Cu3BiSe3) are investigated with the screened hybrid exchange-correlation functional HSE06 and their candidacy for use as absorber materials assessed. The materials are shown to exhibit low VBM effective masses, due partially to the presence of lone pairs that originate from the Sb and Bi states. Although all four materials possess indirect fundamental band gaps, calculated optical absorbance shows direct transitions close in energy. Optical band gaps within the visible-light spectrum are also predicted for three of the systems, (Cu3SbSe3, Cu3BiS3 and Cu3BiSe3) making them promising candidates for PV applications.