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The resulting material demonstrated a significant improvement in the true ultimate tensile strength (∼1300 MPa) with good uniform elongation (∼23%), as compared to conventional TRIP steels.
The sensor material demonstrated a wide linear range of 0.8 200 mM chloride and a diffusion-limited response time; sweat chloride levels corresponded to measurable changes in fluorescence emission that was captured by a smartphone.
Furthermore, specimens with silicon as the cellular interface material demonstrated a 33% reduction in proximal crater damage across all specimen sizes tested, with up to 10% increase in penetration depth.
Temperature regimes at 5 and 10 mm below the surface of each material demonstrated a consistent and statistically significant negative relationship between barnacle abundance and indicators of thermal breakdown.
The layer structured hybrid material demonstrated a superior electrochemical performance due to the synergistic effect from the pseudocapacitance of Ni-Al LDH and the electrical double layer capacitance of graphene.
The MWCNT-grafted material demonstrated a non-continuous and very thin polypyrrole coating onto the carbon surface.
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The resulting material demonstrates a significant improvement in the ultimate tensile strength (1077 MPa) with good uniform elongation (22.5%), as compared to conventional TRIP steels.
The resulting LiNi0.2Mn0.6Co0.2O2 cathode material demonstrates a durable performance with an initial discharge specific capacity of 258 mAh g−1 while maintaining above 210 mAh g−1 after 50 cycles.
The resultant composite material demonstrates a homogeneous distribution of constituents over the submicron particles and a unique hollow spherical microstructure, which provides an enhanced electrical conductivity and better accommodation of volume change of silicon during electrochemical charge discharge cycling, respectively.
It was found that a-EHC material is the less amorphous material, demonstrating a higher capacitance (120 μF cm−2), higher amount of reducible and oxidizable functional groups, higher ability for the H2O2 reduction (180.7 and 4.3 μA cm−2 mM−1 sensitivity at −1.1 V and at −0.50 V, respectively) and superior catalytic activity for the ORR (17 A g−1 at −0.30 V).
Benefiting from reasonable molecular design and appropriate control of conductive carbon, the as-prepared material demonstrates a high reversible capacity (921 mA h g−1 at 50 mA g−1), good rate capability (207 mA h g−1 at 5 A g−1) and long-term cycling stability (remaining retention of around 78% after 400 cycles at 500 mA g−1).
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