Combining theory and experiment in electrocatalysis: Insights into materials design

Better living through water-splitting Chemists have known how to use electricity to split water into hydrogen and oxygen for more than 200 years. Nonetheless, because the electrochemical route is inefficient, most of the hydrogen made nowadays comes from natural gas. Seh et al. review recent progress in electrocatalyst development to accelerate water-splitting, the reverse reactions that underlie fuel cells, and related oxygen, nitrogen, and carbon dioxide reductions. A unified theoretical framework highlights the need for catalyst design strategies that selectively stabilize distinct reaction intermediates relative to each other. Science , this issue p. 10.1126/science.aad4998 </jats:p

Two-Dimensional Titanium and Molybdenum Carbide MXenes as Electrocatalysts for CO2 Reduction

Electrocatalytic CO2 reduction reaction (CO2RR) is an attractive way to produce renewable fuel and chemical feedstock, especially when coupled with efficient CO2 capture and clean energy sources. On the fundamental side, research on improving CO2RR activity still revolves around late transition metal-based catalysts, which are limited by unfavorable scaling relations despite intense investigation. Here, we report a combined experimental and theoretical investigation into electrocatalytic CO2RR on Ti- and Mo-based MXene catalysts. Formic acid is found as the main product on Ti2CTx and Mo2CTx MXenes, with peak Faradaic efficiency of over 56% on Ti2CTx and partial current density of up to −2.5 mA cm−2 on Mo2CTx. Furthermore, simulations reveal the critical role of the Tx group: a smaller overpotential is found to occur at lower amounts of –F termination. This work represents an important step toward experimental demonstration of MXenes for more complex electrocatalytic reactions in the future

Adult day care provision in Kuching, Sarawak : Positive aging or social isolation?

Ageing is a barrier for old people to fully engage in social activities. The population of senior citizens is growing at a fast pace globally. Therefore, certain organizations have been making effort to ensure that they stay happily and contribute to society, thus reducing social problems. One of the services organized is adult day care services. Due to the modern medical technology and professional health care system, the longevity of a person has advanced. The purpose of this research is to investigate the role of adult day care services in this modern era. The samples of this research were eight senior citizens and ten care workers. This research was carried out in five branches of Kenneth Care home which are located in Kuching, Sarawak. This study used qualitative method to get more information and detail answers from the respondents. Indepth interview using questionnaires and systematic observation were utilised in this research. Findings of this study show that the use of adult day care in Kuching is not attractive and conducive to the respondents. Moreover, the majority of the respondents showed great concerns about the provision of services. This study would benefit the care-workers, the senior citizens, and their stakeholders. Subsequently, it will help to improve the provision provided

Antimicrobial Drug Resistance in Pathogens Causing Nosocomial Infections at a University Hospital in Taiwan, 1981-1999

To determine the distribution and antimicrobial drug resistance in bacterial pathogens causing nosocomial infections, surveillance data on nosocomial infections documented from 1981 to 1999 at National Taiwan University Hospital were analyzed. During this period, 35,580 bacterial pathogens causing nosocomial infections were identified. Candida species increased considerably, ranking first by 1999 in the incidence of pathogens causing all nosocomial infections, followed by Staphylococcus aureus and Pseudomonas aeruginosa. Candida species also increased in importance as bloodstream infection isolates, from 1.0% in 1981-1986 to 16.2% in 1999. The most frequent isolates from urinary tract infections were Candida species (23.6%), followed by Escherichia coli (18.6%) and P. aeruginosa (11.0%). P. aeruginosa remained the most frequent isolates for respiratory tract and surgical site infections in the past 13 years. A remarkable increase in incidence was found in methicillin-resistant S. aureus (from 4.3% in 1981-1986 to 58.9% in 1993-1998), cefotaxime-resistant E. coli (from 0% in 1981-1986 to 6.1% in 1993-1998), and cefotaxime-resistant Klebsiella pneumoniae (from 4.0% in 1981-1986 to 25.8% in 1993-1998). Etiologic shifts in nosocomial infections and an upsurge of antimicrobial resistance among these pathogens, particularly those isolated from intensive care units, are impressive and alarming

Factors affecting students' acceptance of SMART2 learning management system

The aims of this study is to inspect the factors affecting students' acceptance of SMART2 Learning Management System. This study applied a multiple regression for data analysis covering a sample of 218 respondents. Results revealed that the proposed hypothesis via multiple regressions validated that the acceptance and usage of SMART2 UMS was effected positively by the use behaviour. Research outcomes may benefit the learning management system market involving SMART2 UMS in developing constructive strategies to evaluate the usage behaviour of students in UMSLIC in using the SMART2 UMS learning management system and assess the acceptance level of students of SMART2 UMS towards the use behaviour. The consequences of this research study offer a new towards the front movement to the discoveries of advanced studies on acceptance and use behaviour, which is not revealed much in the literature in the state of affairs of UMSLIC by providing extra details in tapering the research space with considerations to comprehend the acceptance and usage of the SMART2 UMS

Electrode roughness dependent electrodeposition of sodium at the nanoscale

Na metal is an attractive anode material for rechargeable Na ion batteries, however, the dendritic growth of Na can cause serious safety issues. Along with modifications of solid-electrolyte interphase (SEI), engineering the electrode has been reported to be effective in suppressing Na dendritic growth, likely by reducing localized current density accumulation. However, fundamental understanding of Na growth at the nanoscale is still limited. Here, we report an in-situ study of Na electrodeposition in electrochemical liquid cells with the electrodes in different surface roughness, e.g., flat or sharp curvature. Real time observation using transmission electron microscopy (TEM) reveals the Na electrodeposition with remarkable details. Relatively large Na grains (in the micrometer scale) are achieved on the flat electrode surface. The local SEI thickness variations impact the growth rate, thus the morphology of individual grains. In contrast, small Na grains (in tens of nanometers) grow explosively on the electrode at the point with sharp curvature. The newly formed Na grains preferentially deposit at the base of existing grains close to the electrode. Further studies using continuum-based computational modeling suggest that the growth mode of an alkali metal (e.g. Na) is strongly influenced by the transport properties of SEI. Our direct observation of Na deposition in combination with the theoretical modeling provides insights for comprehensive understanding of electrode roughness and SEI effects on Na electrochemical deposition

Polypyrrole/TiO2 nanotube arrays with coaxial heterogeneous structure as sulfur hosts for lithium sulfur batteries

The lithium-sulfur cell has shown great prospects for future energy conversion and storage systems due to the high theoretical specific capacity of sulfur, 1675 mAh g−1. However, it has been hindered by rapid capacity decay and low energy efficiency. In this work, polypyrrole (PPy)/TiO2 nanotubes with coaxial heterogeneous structure as the substrate of the cathode is prepared and used to improve the electrochemical performance of sulfur electrodes. TiO2 nanotubes decorated with PPy provide a highly ordered conductive framework for Li+ ion diffusion and reaction with sulfur. This architecture also is helpful for trapping the produced polysulfides, and as a result attenuates the capacity decay. Furthermore, the heat treatment temperature used in the sulfur loading process has been confirmed to have an important impact on the overall performance of the resultant cell. The as-designed S/PPy/TiO2 nanotube cathode using an elevated heating temperature shows excellent cycling stability with a high discharge capacity of 1150 mAh g−1 and average coulombic efficiency of 96% after 100 cycles

Advances in the Synthesis and Long-Term Protection of Zero-Valent Iron Nanoparticles

Core@shell Fe@Fe3O4 NPs are synthesized via the thermal decomposition of iron pentacarbonyl (Fe(CO)5) in the presence either of oleylamine (OAm) or a mixture of OAm and oleic acid (OA). The heterostructured nanocomposites formed do so by a post-synthetic modification of isolated Fe seeds. This proves the versatility of the coating procedure and represents a significant advantage over previous work with Co seeds owing to the higher magnetic susceptibility, reduced toxicity, and excellent biocompatibility of Fe. Furthermore, the latter system allows the synthetic methodology to be developed from a two-pot scenario where seeds are isolated then coated, to an easier and more efficient direct one-pot scenario. The two-pot method yields proportionately larger cores. However, in both cases, the monodisperse product reveals a carbonaceous interface between the Fe core and oxide shell. Meanwhile for the one-pot synthesis, the OA:OAm ratio influences both the morphology and dispersity of the product. This is interpreted in terms of competing interactions of the ligands with the iron precursor. Superparamagnetism (SPM) is observed, and microscopic studies reveal oxidative stability of the Fe(0) cores achieved by either method for >6 months. It is proposed that the carbonaceous interface is critical to this sustained oxidative stability

Rational Design of Two-Dimensional Transition Metal Carbide/Nitride (MXene) Hybrids and Nanocomposites for Catalytic Energy Storage and Conversion

Electro-, photo-, and photoelectrocatalysis play a critical role toward the realization of a sustainable energy economy. They facilitate numerous redox reactions in energy storage and conversion systems, enabling the production of chemical feedstock and clean fuels from abundant resources like water, carbon dioxide, and nitrogen. One major obstacle for their large-scale implementation is the scarcity of cost-effective, durable, and efficient catalysts. A family of two-dimensional transition metal carbides, nitrides, and carbonitrides (MXenes) has recently emerged as promising earth-abundant candidates for large-area catalytic energy storage and conversion due to their unique properties of hydrophilicity, high metallic conductivity, and ease of production by solution processing. To take full advantage of these desirable properties, MXenes have been combined with other materials to form MXene hybrids with significantly enhanced catalytic performances beyond the sum of their individual components. MXene hybridization tunes the electronic structure toward optimal binding of redox active species to improve intrinsic activity while increasing the density and accessibility of active sites. This review outlines recent strategies in the design of MXene hybrids for industrially relevant electrocatalytic, photocatalytic, and photoelectrocatalytic applications such as water splitting, metal–air/sulfur batteries, carbon dioxide reduction, and nitrogen reduction. By clarifying the roles of individual material components in the MXene hybrids, we provide design strategies to synergistically couple MXenes with associated materials for highly efficient and durable catalytic applications. We conclude by highlighting key gaps in the current understanding of MXene hybrids to guide future MXene hybrid designs in catalytic energy storage and conversion applications