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. Author manuscript; available in PMC: 2021 Apr 1.
Published in final edited form as: J Am Chem Soc. 2020 Mar 23;142(13):6432–6438. doi: 10.1021/jacs.0c01805

Table 1:

Rest potentials measured vs an Ag/AgCl reference with a 3M KCl bridge, converted to NHE by adding 210 mV.

Description Pt (mV vs NHE) Pd(mV vs NHE) Au(mV vs NHE)
UHV1 Plasma-cleaned films in UHV 435±1251 395±125 695±125
Bare chip 1 mM PB Films under 1 mM phosphate buffer 566.8±3.82 540.7±17 388.4±4.3
Chip/SH-btn Functionalized with thiolated biotin 585.3±0.2 482.3±0.1 242.5±0.7
Chip/SH-btn/SA As above bound by streptavidin 578.9±0.4 460.5±1.9 236.8±0.6
Chip/SH-btn/SA/ϕ29 As above bound by a doubly-biotinylated ϕ29 polymerase 564.4±2.8 393.4±0.2 199.8±2.8
Bare chip (repeat) Films under 1 mM phosphate buffer 567.6±3.3 558.5±1.8 417.2±1.8
Chip/SH-DNP Functionalized with thiolated DNP 534.0±4.1 508.3±0.7 266.4±1.0
Chip/SH-DNP/Ab As above + anti-DNP IgE 537.8±0.7 438.1±0.3 256.1±0.2
1

UHV data were measured to ±4 meV: the error quoted here (125 meV) represents the spread of values currently accepted for the work function of the NHE.

2

Errors reflect stability of rest potential measurement. Repeat measurement (see bare chip repeat) indicates a run-to-run variation of ±5% (the error bars used in Figure 2b).