Table 1.
Device Configurations Used in the Different Laboratories
Name | Junctions Descriptiona | Contact Areac [μm2] |
||
---|---|---|---|---|
Geometric | Uncertainty | Methodb | ||
LOFO-Au | Si/SiOx-linker-protein//LOFO-Au | 2 × 105 | ±10% | Img |
Hg | Si/SiOx-linker-protein//Hg | 5000 | ±5% | Img |
evap-Pb | Si/SiOx-linker-protein//evap-Pb/Au | 5000 | ±10% | Ptr |
th-EGaIn | TSAu-linker-protein//GaOx/th-EGaIn | 1000 | ±10% | Ptr |
μch-EGaIn | TSAu-linker-protein//GaOx/μch-EGaIn | 500 | ±10% | Ptr |
tip-EGaIn | TSAu-linker-protein//GaOx/tip-EGaIn | 300 | ±10% | Img |
Au nanorod | Au-linker-protein//Au nanorod | ~5 × 10−3 | ±50% | AFM Img |
NAB | Carbon-NAB//evap-C//Au | 1.25× 105 | ±10% | Ptr |
Protein: ferritin, PSI; bR.
Img or Ptr mark whether the geometric area was obtained from a microscopy image (Img) or AFM tapping mode imaging (AFM Img) or dictated by feature patterning (Ptr).
Refer to Figure 1.
mg or Ptr mark whether the geometric area was obtained from a microscopy image (Img) or AFM tapping mode imaging (AFM Img) or dictated by feature patterning (Ptr).
Refer to Figure 2.