Extreme heat events with wet-bulb temperatures (WBT) above 35°C pose serious risks to human survival, and conventional hydrogel evaporative cooling alone may not provide sufficient relief as it must be maintained...
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Carbon nanotubes (CNTs) are quasi-one dimensional nanostructures that display both high thermal conductivity for potential thermal management applications and intriguing low-dimensional phonon transport phenomena. In ...
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Models to describe electrical conduction in quantum dot (QD) constituted films often overlook the effects of geometric disorder. We address related issues by examining the influence of the QD packing fraction (PF) on ...
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Alloying element segregation often occurs under a reactive environment but its interplay with the subsequent surface oxidation of the alloy remains unclear. Using synchrotron-based ambient-pressure x-ray photoelectron...
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Alloying element segregation often occurs under a reactive environment but its interplay with the subsequent surface oxidation of the alloy remains unclear. Using synchrotron-based ambient-pressure x-ray photoelectron spectroscopy, we dynamically monitor the surface segregation in Cu3Pt(100) in response to temperature and oxygen gas. Vacuum annealing leads to surface segregation of Cu along with the enrichment of Pt in the subsurface region. Upon switching to the O2 atmosphere, dissociative chemisorption of oxygen does not change the surface segregation profile from that under the vacuum annealing condition. A stepwise increase in the oxygen pressure results in the transformation pathway of Cu→Cu2O→CuO, in which the selective oxidation of Cu gives rise to further accumulation of Pt underneath the oxide/alloy interface that hinders the supply of Cu from the bulk to the oxide/alloy interface, thereby leading to the termination of the surface oxidation after the Cu2O→CuO conversion is completed. This differs from the transformation pathway of Cu→Cu2O→Cu2O/CuO for the oxidation of pure Cu and Cu-Au alloys, in which the oxidation of Cu continues and the Cu2O/CuO bilayer growth is constantly maintained. These key differences provide useful insight into alloy design for controlling the surface properties such as corrosion resistance and catalytic performance of Cu base alloys.
Passive transformation of waves via nonlinear systems is ubiquitous in settings ranging from acoustics to optics and electromagnetics. Passivity is of particular importance for responding rapidly to stimuli and nonlin...
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Alloy oxidation is complex and involves several critical processes that lack understanding on the atomic level. Here, we report an atomistic picture of the initial-stage oxidation of stepped Cu3Au(100) using a combina...
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Alloy oxidation is complex and involves several critical processes that lack understanding on the atomic level. Here, we report an atomistic picture of the initial-stage oxidation of stepped Cu3Au(100) using a combination of surface science tools and modeling to illuminate the microscopic processes underlying oxygen-adsorption-induced structural and compositional changes. Pristine Cu3Au(100) consists of wide CuAu-terminated terraces and narrow Cu-terminated terraces separated by monatomic steps. Counterintuitive to the common expectations of the adsorbate-induced surface segregation of the more reactive alloy component, our observations demonstrate that the oxygen adsorption leads to the exfoliation of the outermost CuAu layer, thereby exposing the inner Cu plane to O attack. This occurs via the oxygen-assisted abstraction of Au and Cu atoms from step edges and CuAu terraces, which generates many Cu adatoms aggregating into Cu clusters and Au adatoms dissolving into the bulk. The oxygen adsorption onto fourfold hollow sites of the exposed Cu plane results in nucleation and growth of the c(2×2)−O superstructure, which can be fit well by the Johnson-Mehl-Avrami-Kolmogorov theory with a site-saturated nucleation mechanism.
In this paper, some adaptive single-step methods like Trapezoid (TR), Implicit-mid point (IMP), Euler-backward (EB), and Radau IIA (Rad) methods are implemented in Maple to solve index-1 nonlinear Differential Algebra...
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Rapid, sensitive, multiplexed antibody detection technologies are essential for assessing vaccine efficacy and recipient immunity against viruses. As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) varian...
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The extensive commercialization of practical solid-state batteries (SSBs) necessitates the development of high-loading solid-state cathodes with fast charging capability. However, electrochemical kinetics are severely...
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The extensive commercialization of practical solid-state batteries (SSBs) necessitates the development of high-loading solid-state cathodes with fast charging capability. However, electrochemical kinetics are severely delayed in thick cathodes due to tortuous ion transport pathways and slow solid-solid ion diffusion, which limit the achievable capacity of SSBs at high current densities. In this work, we propose a conductivity gradient cathode with low-tortuosity to enable facile ion transport and counterbalance ion concentration gradient, thereby overcoming the kinetic limitations and achieving fast charging capabilities in thick cathodes. The LiNi 0.8 Co 0.1 Mn 0.1 O 2 cathodes deliver a room-temperature (RT) capacities of 147 and 110 mAh g −1 at 5 C and 10 C, respectively, and meanwhile achieve a RT areal capacity of 3.3 mAh cm −2 at 3 C, enabling SSBs simultaneously high energy and power densities. The universality of this strategy is demonstrated in LiFePO 4 cathodes, providing a novel solution for fast charging and large-scale application of high-loading SSBs.
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