TY - JOUR
T1 - Hard-Wired Solid-State Bioelectronic Micropore Devices
T2 - Permanent Metal-Protein-Metal Junction Proof-of-Concept
AU - Bera, Sudipta
AU - Mishuk, Eran
AU - Li, Ping'an
AU - Das, Sourav
AU - Keshet, Sigal
AU - Garusi, Sharon
AU - Tunik, Leonid
AU - Edri, Eran
AU - Selzer, Yoram
AU - Pecht, Israel
AU - Vilan, Ayelet
AU - Sheves, Mordechai
AU - Cahen, David
N1 - Publisher Copyright:
© 2025 The Author(s). Small published by Wiley-VCH GmbH.
PY - 2025/12/10
Y1 - 2025/12/10
N2 - The design, fabrication, and application of robust metal/protein/metal junctions are presented with ultrathin (≈20 nm) protein films demonstrating long-term stability in ambient conditions and preserving their electron transport behavior also at ≈10 K. These junctions establish a reliable platform with a permanent contact configuration, where the confined protein layer retains its functional activity after metal contact evaporation on the protein. A bottom-up micropore device (MpD) fabrication strategy is used and optimized to ensure reproducibility. The sub-nanometer roughness of the bottom electrode is preserved within the micropore, enabling uniform protein layer deposition and film formation. In the MpD structures, protein layers are integrated between Au-covered substrates and an e-beam evaporated Pd contacts. Depositing multi-layered protein films allows for defining film widths, as tested by the atomic force microscopy (AFM)-based scratching technique. The films are composed of human serum albumin (HSA) and bacteriorhodopsin (bR). Pd's preferred 2D growth minimized metal penetration and short circuits. Impedance phase response analysis shows that ≈60% of the junctions are functional ones, demonstrating the effectiveness of the fabrication approach. These protein-based MpD junctions provide a basis for future stable platforms for electron transport studies of bio- and other soft materials.
AB - The design, fabrication, and application of robust metal/protein/metal junctions are presented with ultrathin (≈20 nm) protein films demonstrating long-term stability in ambient conditions and preserving their electron transport behavior also at ≈10 K. These junctions establish a reliable platform with a permanent contact configuration, where the confined protein layer retains its functional activity after metal contact evaporation on the protein. A bottom-up micropore device (MpD) fabrication strategy is used and optimized to ensure reproducibility. The sub-nanometer roughness of the bottom electrode is preserved within the micropore, enabling uniform protein layer deposition and film formation. In the MpD structures, protein layers are integrated between Au-covered substrates and an e-beam evaporated Pd contacts. Depositing multi-layered protein films allows for defining film widths, as tested by the atomic force microscopy (AFM)-based scratching technique. The films are composed of human serum albumin (HSA) and bacteriorhodopsin (bR). Pd's preferred 2D growth minimized metal penetration and short circuits. Impedance phase response analysis shows that ≈60% of the junctions are functional ones, demonstrating the effectiveness of the fabrication approach. These protein-based MpD junctions provide a basis for future stable platforms for electron transport studies of bio- and other soft materials.
KW - biomolecular electronics
KW - evaporated top-contact
KW - impedance
KW - micropore device
KW - permanent contact
KW - protein thin film
UR - https://www.scopus.com/pages/publications/105019259095
U2 - 10.1002/smll.202506560
DO - 10.1002/smll.202506560
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 41110151
AN - SCOPUS:105019259095
SN - 1613-6810
VL - 21
JO - Small
JF - Small
IS - 49
M1 - e06560
ER -