Publications by authors named "S C Risse"

Sn-based electrodes are promising candidates for next-generation lithium-ion batteries. However, it suffers from deleterious micro-structural deformation as it undergoes drastic volume changes upon lithium insertion and extraction. Progress in designing these materials is limited to complex structures.

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Maximal isometric contraction time (MICT) is critical for most motor tasks and depends on skeletal muscle blood flow at < 40% of maximal voluntary strength (MVC). Whether limb work positions associated with reduced perfusion pressure and facilitated vessel compression affect MICT is largely unknown. In 14 healthy young men we therefore assessed bilateral handgrip MICT at 15, 20, 30, 40, and 70% of MVC in horizontal forearm positions of 0.

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We present what we believe to be a novel, geometrically scalable manufacturing method for creating compact, low-resonance frequency, and high quality factor fused silica resonators. These resonators are intended to be used in inertial sensors for measuring external disturbances of sensitive physics experiments. The novel method uses direct bonding and chemical-mechanical polishing (CMP) in order to overcome the limitations of current subtractive manufacturing methods, which face prohibitive cost and complexity as material removal increases, inherently restricting the design flexibility of the resonator.

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Sulfur/carbon copolymers have emerged as promising alternatives for conventional crystalline sulfur cathodes for lithium-sulfur batteries. Among these, sulfur-n-1,3-diisopropenylbenzene (S/DIB) copolymers, which present a 3D network of DIB molecules interconnected via sulfur chains, have particularly shown a good performance and, therefore, have been under intensive experimental and theoretical investigations. However, their structural complexity and flexibility have hindered a clear understanding of their structural evolution during redox reactions at an atomistic level.

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Background And Aims: Plant Ni uptake in aboveground biomass exceeding concentrations of 1000 μg g in dry weight is defined as Ni hyperaccumulation. Whether hyperaccumulators are capable of mobilizing larger Ni pools than non-accumulators is still debated and rhizosphere processes are still largely unknown. The aim of this study was to investigate rhizosphere processes and possible Ni mobilization by the Ni hyperaccumulator and to test Ni uptake in relation to a soil Ni gradient.

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