Boosting hot electron flux and catalytic activity at metal-oxide interfaces of PtCo bimetallic nanoparticles

Despite numerous studies, the origin of the enhanced catalytic performance of bimetallic nanoparticles (NPs) remains elusive because of the ever-changing surface structures, compositions, and oxidation states of NPs under reaction conditions. An effective strategy for obtaining critical clues for the phenomenon is real-time quantitative detection of hot electrons induced by a chemical reaction on the catalysts. Here, we investigate hot electrons excited on PtCo bimetallic NPs during H-2 oxidation by measuring the chemicurrent on a catalytic nanodiode while changing the Pt composition of the NPs. We reveal that the presence of a CoO/Pt interface enables efficient transport of electrons and higher catalytic activity for PtCo NPs. These results are consistent with theoretical calculations suggesting that lower activation energy and higher exothermicity are required for the reaction at the CoO/Pt interface

Synthesis of Well-Defined, Surfactant-Free Co₃O₄ Nanoparticles:The Impact of Size and Manganese Promotion on Co₃O₄ Reduction and Water Oxidation Activity

Abstract: A surfactant-free synthetic route has been developed to produce size-controlled, cube-like cobalt oxide nanoparticles of three different sizes in high yields. It was found that by using sodium nitrite as salt-mediating agent, near-quantitative yields could be obtained. The size of the nanoparticles could be altered from 11 to 22 nm by changing the cobalt concentration and reaction time. These surfactant-free nanoparticles form ideal substrates for facile deposition of further elements such as manganese. The effect of size of the cobalt oxide nanoparticles and the presence of manganese on the reducibility of cobalt oxide to metallic cobalt was investigated. Similarly, the effect of these parameters was investigated with a visible light promoted water oxidation system with cobalt oxide as catalyst, together with [Ru(bpy) 3] 2+ light harvester dye and an electron acceptor. Graphical Abstract: A novel surfactant-free synthetic route has been developed to produce size-controlled, cube shaped cobalt oxide nanoparticles in high yields. [Figure not available: see fulltext.]. </p

Volatile diterpene emission by two Mediterranean Cistaceae shrubs

Mediterranean vegetation emits a wide range of biogenic volatile organic compounds (BVOCs) among which isoprenoids present quantitatively the most important compound class. Here, we investigated the isoprenoid emission from two Mediterranean Cistaceae shrubs, Halimium halimifolium and Cistus ladanifer, under controlled and natural conditions, respectively. For the first time, diurnal emission patterns of the diterpene kaurene were detected in real-time by Proton-Transfer-Reaction-Timeof- Flight-Mass-Spectrometer. Kaurene emissions were strongly variable among H. halimifolium plants, ranging from 0.01 ± 0.003 to 0.06 ± 0.01 nmol m−2 s−1 in low and high emitting individuals, respectively. They were in the same order of magnitude as monoterpene (0.01 ± 0.01 to 0.11 ± 0.04 nmol m−2 s−1) and sesquiterpene (0.01 ± 0.01 to 0.52 nmol m−2 s−1) emission rates. Comparable range and variability was found for C. ladanifer under natural conditions. Labelling with 13C-pyruvate suggested that emitted kaurene was not derived from de novo biosynthesis. The high kaurene content in leaves, the weak relationship with ecophysiological parameters and the tendency of higher emissions with increasing temperatures in the field indicate an emission from storage pools. This study highlights significant emissions of kaurene from two Mediterranean shrub species, indicating that the release of diterpenes into the atmosphere should probably deserve more attention in the futureinfo:eu-repo/semantics/publishedVersio

A SIMPLIFIED THERMODYNAMIC ANALYSIS OF A LiBr-H 2 O VERTICAL TUBE ABSORBER

ABSTRACT One of the most important components of an absorption airconditioning/heat pump system is the absorber, where the refrigerant water vapour is absorbed into the liquid solution. While absorption systems have been in use for several years, the complex transport phenomena occurring in the absorber are not fully elucidated yet. Thus, an attempt is made to model the absorption process of water vapour in aqueous solutions of lithium bromide considering a falling-film, vertical-tube absorber. The proposed analysis is based on the formulation of four differential equations describing the spatial variation (parallel to the tube-axis) of solution mass, temperature, mass fraction and coolant temperature. The system of ordinary differential equations is numerically solved using a non-stiff numerical method. Thermophysical properties and especially, heat and mass transfer coefficients are calculated using widelyaccepted and reliable relationships, which are extracted from the literature using recently published information on wavylaminar flows. In the present study, the questionable assumption of treating the water vapour as an ideal gas is heavily modified utilizing. Consequently, the hypothesis of saturated water vapour at the steam-solution interaction surface is revised by introducing an energy difference between the superheated steam and the liquid water within the binary solution. The last correction encouraged us to compare theoretical results for solution temperature, mass fraction and mass flow rate, which were obtained using both assumptions. It was proved that the initial treatment causes an underestimation of the absorbed steam mass and correspondingly, an underestimation of solution temperature and mass fraction at the mass exchange interface. An attempt is made also to identify the effect of mass transfer coefficient on the effectiveness of the absorption process and on the energy differences between the superheated steam and the liquid water either as pure substance or as component of the binary mixture. It was shown that the increase of mass transfer coefficient leads to an increase of steam mass transfer rate and to a corresponding decrease of solution temperature slope at the entrance of a tube. Correspondingly, the increase of mass transfer coefficient results in an increase of heat of absorption and heat of dilution at the same variation range of the solution mass fraction

Data for: Recombinant production of labdane-type diterpenes in the green alga Chlamydomonas reinhardtii

Alignment of CcCLS anbd CoCL

Towards AI driven environmental sustainability: an application of automated logistics in container port terminals

Artificial intelligence and data analytics capabilities have enabled the introduction of automation, such as robotics and Automated Guided Vehicles (AGVs), across different sectors of the production spectrum which successively has profound implications for operational efficiency and productivity. However, the environmental sustainability implications of such innovations have not been yet extensively addressed in the extant literature. This study evaluates the use of AGVs in container terminals by investigating the environmental sustainability gains that arise from the adoption of artificial intelligence and automation for shoreside operations at freight ports. Through a comprehensive literature review, we reveal this research gap across the use of artificial intelligence and decision support systems, as well as optimisation models. A real-world container terminal is used, as a case study in a simulation environment, on Europe’s fastest-growing container port (Piraeus), to quantify the environmental benefits related to routing scenarios via different types of AGVs. Our study contributes to the cross-section of operations management and artificial intelligence literature by articulating design principles to inform effective digital technology interventions at non-automated port terminals, both at operational and management levels