journal article·2024Open access

Photosystem I complexes form remarkably stable self-assembled tunneling junctions

Nahid Torabi, Ryan C. Chiechi

Nanoscale· Volume 16· Issue 41

Abstract

This paper describes large-area molecular tunneling junctions comprising self-assembled monolayers (SAMs) of light-harvesting protein complexes using eutectic Ga-In (EGaIn) as a top contact. The complexes, which are readily isolable in large quantities from spinach leaves, self-assemble on top of SAMs of [6,6]-phenyl-C61-butyric acid (PCBA) on gold (Au) supported by mica substrates (AuMica), which induces them to adopt a preferred orientation with respect to the electron transport chain that runs across the short axis of each complex, leading to temperature-independent rectification. We compared trimeric protein complexes isolated from thermophilic cyanobacteria to monomeric complexes extracted from spinach leaves by measuring charge-transport at variable temperatures and over the course of at least three months. Transport is independent of temperature in the range of 130 to 310 K for both protein complexes, affirming that the likely mechanism is non-resonant tunneling. The junctions rectified current and were stable for at least three months when stored at room temperature in ambient conditions, with the yield of working junctions falling from 100% to 97% over that time. These results demonstrate a straightforward strategy for forming remarkably robust molecular junctions, avoiding the fragility that is common in molecular electronics.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Photosynthetic Processes and Mechanisms · Spectroscopy and Quantum Chemical Studies · Molecular Junctions and Nanostructures

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands

Department of Chemistry & Organic and Carbon Electronics Cluster, North Carolina State University, Raleigh, North Carolina 27695-8204, USA

References (89)

Show source-provided references
1. Vilan · Chem. Rev. · 2017 · 117 · 424810.1021/acs.chemrev.6b00595 ↗
2. Nitzan · Science · 2003 · 300 · 138410.1126/science.1081572 ↗
3. Adams · J. Phys. Chem. B · 2003 · 107 · 666810.1021/jp0268462 ↗
4. Liu · Chem. Phys. Rev. · 2021 · 2 · 02130310.1063/5.0050667 ↗
5. X.Liu , H.Yang , H.Harb , R.Samajdar , T. J.Woods , O.Lin , Q.Chen , A. I. B.Romo , J.Rodríguez-López , R. S.Assary , J. S.Moore and C. M.Schroeder
6. Li · Nano Lett. · 2021 · 21 · 834010.1021/acs.nanolett.1c02915 ↗
7. B.Lawson , E.Vidal , M. M.Haley and M.Kamenetska , Extreme anti-ohmic conductance enhancement in neutral diradical acene-like molecular junctions , 2024 , 10.48550/ARXIV.2403.0490610.48550/ARXIV.2403.04906 ↗
8. B.Lawson , E.Vidal , M. M.Haley and M.Kamenetska , Extreme anti-ohmic conductance enhancement in neutral diradical acene-like molecular junctions , 2024 , 10.48550/ARXIV.2403.0490610.48550/ARXIV.2403.04906 ↗
9. Pan · Nano Lett. · 2023 · 23 · 693710.1021/acs.nanolett.3c01540 ↗
10. Skipper · J. Am. Chem. Soc. · 2021 · 143 · 1643910.1021/acs.nanolett.3c01540 ↗
11. Skipper · ACS Nano · 2023 · 17 · 1610710.1021/acsnano.3c04963 ↗
12. Al-Owaedi · Nanoscale · 2017 · 9 · 990210.1039/c7nr01829k ↗
13. Herrer · Adv. Mater. Interfaces · 2023 · 10 · 230013310.1002/admi.202300133 ↗
14. Operamolla · J. Mater. Chem. C · 2015 · 3 · 647110.1039/c5tc00775e ↗
15. Kothe · Angew. Chem., Int. Ed. · 2013 · 52 · 1423310.1002/anie.201303671 ↗
16. Giardi · Trends Biotechnol. · 2005 · 23 · 25710.1016/j.tibtech.2005.03.003 ↗
17. Romero-Muñiz · Biomolecules · 2019 · 9 · 50610.3390/biom9090506 ↗
18. Ing · J. Phys. Chem. B · 2018 · 122 · 1040310.1021/acs.jpcb.8b07431 ↗
19. Amdursky · Adv. Mater. · 2014 · 26 · 714210.1002/adma.201402304 ↗
20. Fereiro · J. Am. Chem. Soc. · 2020 · 142 · 1921710.1021/jacs.0c08836 ↗
21. Garg · Chem. Sci. · 2018 · 9 · 730410.1039/c8sc01716f ↗
22. Fereiro · Proc. Natl. Acad. Sci. U. S. A. · 2018 · 115 · E457710.1073/pnas.1719867115 ↗
23. Shinwari · Adv. Funct. Mater. · 2010 · 20 · 186510.1002/adfm.200902066 ↗
24. Saxena · J. Am. Chem. Soc. · 2020 · 142 · 1542010.1021/jacs.0c06764 ↗
25. Futera · J. Phys. Chem. Lett. · 2020 · 11 · 976610.1021/acs.jpclett.0c02686 ↗
26. Kayser · J. Phys. Chem. Lett. · 2019 · 11 · 14410.1021/acs.jpclett.9b03120 ↗
27. Ruiz · J. Am. Chem. Soc. · 2017 · 139 · 1533710.1021/jacs.7b06130 ↗
28. Gray · Proc. Natl. Acad. Sci. U. S. A. · 2005 · 102 · 353410.1073/pnas.0408029102 ↗
29. Chi · J. Am. Chem. Soc. · 2000 · 122 · 404710.1021/ja993174t ↗
30. Amdursky · Phys. Chem. Chem. Phys. · 2013 · 15 · 1714210.1039/c3cp52885e ↗
31. Koch · Nat. Nanotechnol. · 2012 · 7 · 71310.1038/nnano.2012.169 ↗
32. Kumar · Adv. Mater. · 2015 · 28 · 182410.1002/adma.201504402 ↗
33. Ocampo · J. Am. Chem. Soc. · 2015 · 137 · 841910.1021/jacs.5b01241 ↗
34. Yan · Proc. Natl. Acad. Sci. U. S. A. · 2013 · 110 · 532610.1073/pnas.1221643110 ↗
35. Bera · J. Am. Chem. Soc. · 2023 · 2482010.1021/jacs.3c09120 ↗
36. Gordiichuk · Adv. Sci. · 2017 · 4 · 160039310.1002/advs.201600393 ↗
37. Qiu · Nat. Mater. · 2020 · 19 · 33010.1038/s41563-019-0587-x ↗
38. Torabi · Langmuir · 2021 · 37 · 1146510.1021/acs.langmuir.1c01542 ↗
39. Jordan · Nature · 2001 · 411 · 90910.1038/35082000 ↗
40. Chitnis · Annu. Rev. Plant Physiol. Plant Mol. Biol. · 2001 · 52 · 59310.1146/annurev.arplant.52.1.593 ↗
41. Ben-Shem · Nature · 2003 · 426 · 63010.1038/nature02200 ↗
42. Wang · Adv. Energy Mater. · 2021 · 11 · 210285810.1002/aenm.202102858 ↗
43. Şener · J. Chem. Phys. · 2004 · 120 · 1118310.1063/1.1739400 ↗
44. P.Fromme , E.Schlodder and S.Jansson , Light-Harvesting Antennas in Photosynthesis , Springer Netherlands , 2003 , pp. 253–279 , 10.1007/978-94-017-2087-8_810.1007/978-94-017-2087-8_8 ↗
45. Kitmitto · J. Biol. Chem. · 1998 · 273 · 2959210.1074/jbc.273.45.29592 ↗
46. Kouřil · Photochem. Photobiol. Sci. · 2005 · 4 · 109110.1039/b505519a ↗
47. Gardian · Biochim. Biophys. Acta, Bioenerg. · 2007 · 1767 · 72510.1016/j.bbabio.2007.01.021 ↗
48. Klimmek · Biochemistry · 2005 · 44 · 306510.1021/bi047873g ↗
49. Şener · Biophys. J. · 2005 · 89 · 163010.1529/biophysj.105.066464 ↗
50. Bibby · Nature · 2001 · 412 · 74310.1038/35089098 ↗
51. Bibby · J. Biol. Chem. · 2001 · 276 · 4324610.1074/jbc.m106541200 ↗
52. Boekema · Nature · 2001 · 412 · 74510.1038/35089104 ↗
53. Melkozernov · J. Phys. Chem. B · 2004 · 108 · 1054710.1021/jp049375n ↗
54. Liu · J. Power Sources · 2021 · 506 · 23025110.1016/j.jpowsour.2021.230251 ↗
55. Brecht · Biochim. Biophys. Acta, Bioenerg. · 2012 · 1817 · 44510.1016/j.bbabio.2011.11.012 ↗
56. Bibby · Nature · 2003 · 424 · 105110.1038/nature01933 ↗
57. Bombelli · Adv. Energy Mater. · 2014 · 5 · 140129910.1002/aenm.201401299 ↗
58. Liu · ACS Appl. Energy Mater. · 2020 · 3 · 1022410.1021/acsaem.0c02054 ↗
59. Fereiro · J. Phys. Chem. Lett. · 2023 · 14 · 297310.1021/acs.jpclett.2c03700 ↗
60. Qiu · ACS Appl. Mater. Interfaces · 2018 · 10 · 3762510.1021/acsami.8b11115 ↗
61. Gizzie · ACS Appl. Mater. Interfaces · 2015 · 7 · 932810.1021/acsami.5b01065 ↗
62. Stieger · Nanoscale · 2016 · 8 · 1069510.1039/c6nr00097e ↗
63. Ciesielski · Bioresour. Technol. · 2010 · 101 · 304710.1016/j.biortech.2009.12.045 ↗
64. Gordiichuk · Adv. Mater. · 2014 · 26 · 486310.1002/adma.201401135 ↗
65. Qiu · Nat. Commun. · 2022 · 13 · 231210.1038/s41467-022-30038-8 ↗
66. Chiechi · Angew. Chem., Int. Ed. · 2008 · 47 · 14210.1002/anie.200703642 ↗
67. Freer · Nat. Nanotechnol. · 2010 · 5 · 52510.1038/nnano.2010.106 ↗
68. Nijhuis · J. Phys. Chem. C · 2012 · 116 · 1413910.1021/jp303072a ↗
69. Smith · Appl. Phys. Lett. · 2000 · 77 · 139910.1063/1.1290272 ↗
70. Qiu · Adv. Mater. · 2021 · 33 · 200610910.1002/adma.202006109 ↗
71. Kovalchuk · Chem. Sci. · 2016 · 7 · 78110.1039/C5SC03097H ↗
72. Kronemeijer · Appl. Phys. Lett. · 2010 · 97 · 17330210.1063/1.3503607 ↗
73. Hines · J. Am. Chem. Soc. · 2010 · 132 · 1165810.1021/ja1040946 ↗
74. Simmons · J. Appl. Phys. · 1963 · 34 · 179310.1063/1.1702682 ↗
75. Naaman · J. Phys. Chem. Lett. · 2022 · 13 · 1175310.1021/acs.jpclett.2c03141 ↗
76. Puebla-Hellmann · Nature · 2018 · 559 · 23210.1038/s41586-018-0275-z ↗
77. Akkerman · Nature · 2006 · 441 · 6910.1038/nature04699 ↗
78. Akkerman · Org. Electron. · 2010 · 11 · 14610.1016/j.orgel.2009.09.013 ↗
79. McCreery · Acc. Chem. Res. · 2022 · 55 · 276610.1021/acs.accounts.2c00401 ↗
80. Chen · Sci. Adv. · 2023 · 9 · eadh341210.1126/sciadv.adh3412 ↗
81. Mentovich · Nano Lett. · 2009 · 9 · 129610.1021/nl802694k ↗
82. Yuan · J. Am. Chem. Soc. · 2014 · 136 · 655410.1021/ja5007417 ↗
83. Weiss · J. Am. Chem. Soc. · 2007 · 129 · 433610.1021/ja0677261 ↗
84. Qin · Photochem. Photobiol. · 2010 · 87 · 14310.1111/j.1751-1097.2010.00830.x ↗
85. Porra · Biochim. Biophys. Acta, Bioenerg. · 1989 · 975 · 38410.1016/s0005-2728(89)80347-0 ↗
86. Rippka · Microbiology · 1979 · 111 · 110.1099/00221287-111-1-1 ↗
87. El-Mohsnawy · Biochemistry · 2010 · 49 · 474010.1021/bi901807p ↗
88. Mukherjee · Langmuir · 2010 · 26 · 1604810.1021/la102832x ↗
89. Baba · Photosynth. Res. · 1996 · 47 · 12110.1007/bf00016175 ↗