In-Situ STM Visualization of Molecular Structural Evolution during Electrochemical Oxidation Coupling of Para-Aminothiophenol on Au(111)

Zi-Wei Ma , Tai-Rui Wu , An-Ni Zheng , Lai-Ke Chen , Yuan-Hui Xiao , Zhao-Bin Chen , Qing-Na Zheng , Jian-Zhang Zhou , Jia-Wei Yan , De-Yin Wu

Journal of Electrochemistry ›› 2026, Vol. 32 ›› Issue (7) : 2603031

PDF (7190KB)
Journal of Electrochemistry ›› 2026, Vol. 32 ›› Issue (7) :2603031 DOI: 10.61558/2993-074X.3614
ARTICLE
research-article
In-Situ STM Visualization of Molecular Structural Evolution during Electrochemical Oxidation Coupling of Para-Aminothiophenol on Au(111)
Author information +
History +
PDF (7190KB)

Abstract

Para-aminothiophenol (PATP) is not only a widely-used probe molecule in the field of surface-enhanced Raman spectroscopy (SERS), but also an important model molecule for interfacial reactions, exhibiting distinct photo- and electro-oxidation pathways, so that PATP is selectively activated under different external fields. The evolution of products and intermediates during electrochemical oxidative coupling remains unknown. In this study, we have investigated the dynamic electrochemical oxidation process of PATP on the Au(111) surface using cyclic voltammetry, electrochemical (EC)-SERS, and in situ electrochemical scanning tunneling microscopy (EC-STM). The results showed that PATP forms an unsaturated adsorption coverage on Au(111) in an acidic solution. When the potential was positively shifted to the oxidation potential range, the cation radical generated by PATP oxidation alternated with PATP molecules in arrangement. Once the coupling reaction occurred, the adsorption structure of alternating arrangement was transformed into the stripe structure as observed in the STM images. Finally, the coverage on the Au(111) surface decreased and a $\sqrt{3}\times 4\sqrt{6}$. structure was formed. Accordingly, the oxidation reaction product 4′-mercapto-N-phenylquinone diimine (NPQD) would adopt the arrangement of mixed adsorption sites of bridge and hollow sites on Au(111). By determining the adsorption structure evolution of PATP during the electrooxidation process on the gold surface, the mechanism of interfacial electrochemical oxidation coupling reaction is revealed from a spatial perspective. This lays the foundation for further modulation and design of the interfacial reaction of aromatic amine molecules.

Keywords

In situ electrochemical scanning tunneling microscopy / Para-aminothiophenol (PATP) / 4'-mereapto-N-phenylquinone diimine / Electrochemical surface-enhanced Raman spectroscopy

Cite this article

Download citation ▾
Zi-Wei Ma, Tai-Rui Wu, An-Ni Zheng, Lai-Ke Chen, Yuan-Hui Xiao, Zhao-Bin Chen, Qing-Na Zheng, Jian-Zhang Zhou, Jia-Wei Yan, De-Yin Wu. In-Situ STM Visualization of Molecular Structural Evolution during Electrochemical Oxidation Coupling of Para-Aminothiophenol on Au(111). Journal of Electrochemistry, 2026, 32 (7) : 2603031 DOI:10.61558/2993-074X.3614

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Zhang H P, Luo J, Huang H G, Wu L L, Lin Z H. Electrochemical assembly of nano-organized poly-o-phenylenediamine films[J]. Chem. Phys. Lett., 2000, 326(1-2): 169-174. https://doi.org/10.1016/S0009-2614(00)00747-8.

[2]

Li H H, Zhao Y W, Ma L, Ma M H, Jiang J, Wan X B. Radical-carbene coupling reaction: Mn-catalyzed synthesis of indoles from aromatic amines and diazo compounds[J]. Chem. Commun., 2017, 53(44): 5993-5996. https://doi.org/10.1039/C7CC02440A.

[3]

de Pedro Beato E, Priego J, Gironda-Martínez A, González F, Benavides J, Blas J, Martín-Ortega M D, Toledo M Á, Ezquerra J, Torrado A. Mild and efficient palladium-mediated C-N cross-coupling reaction between DNA-conjugated aryl bromides and aromatic amines[J]. ACS Comb. Sci., 2019, 21(2): 69-74. https://doi.org/10.1021/acscombsci.8b00142.

[4]

Ye J X, Wu J L, Lv T T, Wu G L, Gao Y, Chen H J. Oxidative rearrangement coupling reaction for the functionalization of tetrahydro-β-carbolines with aromatic amines[J]. Angew. Chem. Int. Ed., 2017, 56(47): 14968-14972. https://doi.org/10.1002/anie.201708893.

[5]

Zhao L B, Zhang M, Huang Y F, Williams C T, Wu D Y, Ren B, Tian Z Q. Theoretical study of plasmon-enhanced surface catalytic coupling reactions of aromatic amines and nitro compounds[J]. J. Phys. Chem. Lett., 2014, 5(7): 1259-1266. https://doi.org/10.1021/jz5003346.

[6]

Mandal S, Kommula B, Bhattacharyya S. Structural optimization of luminescent sulfur dots for solar light induced efficient and selective oxidative coupling reactions of aromatic amines: A complete metal-free approach[J]. ACS Sustain. Chem. Eng., 2023, 11(41): 14921-14931. https://doi.org/10.1021/acssuschemeng.3c03296.

[7]

Love J C, Estroff L A, Kriebel J K, Nuzzo R G, Whitesides G M. Self-assembled monolayers of thiolates on metals as a form of nanotechnology[J]. Chem. Rev., 2005, 105(4): 1103-1169. https://doi.org/10.1021/cr0300789.

[8]

Wu D Y, Liu X M, Huang Y F, Ren B, Xu X, Tian Z Q. Surface catalytic coupling reaction of p-mercaptoaniline linking to silver nanostructures responsible for abnormal SERS enhancement: A DFT study[J]. J. Phys. Chem. C, 2009, 113(42): 18212-18222. https://doi.org/10.1021/jp9050929.

[9]

Devasenathipathy R, Rani K K, Liu J, Wu D Y, Tian Z Q. Plasmon mediated photoelectrochemical transformations: The example of para-aminothiophenol[J]. Electrochim. Acta, 2021, 367: 137485. https://doi.org/10.1016/j.electacta.2020.137485.

[10]

Huang Y F, Wu D Y, Zhu H P, Zhao L B, Liu G K, Ren B, Tian Z Q. Surface-enhanced Raman spectroscopic study of p-aminothiophenol[J]. Phys. Chem. Chem. Phys., 2012, 14(24): 8485-8497. https://doi.org/10.1039/C2CP40558J.

[11]

Hutchison J A, Centeno S P, Odaka H, Fukumura H, Hofkens J, Uji-i H. Subdiffraction limited, remote excitation of surface enhanced Raman scattering[J]. Nano Lett., 2009, 9(3): 995-1001. https://doi.org/10.1021/nl8030696.

[12]

Ward D R, Halas N J, Ciszek J W, Tour J M, Wu Y, Nordlander P, Natelson D. Simultaneous measurements of electronic conduction and Raman response in molecular junctions[J]. Nano Lett., 2008, 8(3): 919-924. https://doi.org/10.1021/nl073346h.

[13]

Villarreal E, Li G F G, Zhang Q F, Fu X Q, Wang H. Nanoscale surface curvature effects on ligand-nanoparticle interactions: A plasmon-enhanced spectroscopic study of thiolated ligand adsorption, desorption, and exchange on gold nanoparticles[J]. Nano Lett., 2017, 17(7): 4443-4452. https://doi.org/10.1021/acs.nanolett.7b01593.

[14]

Zhong H, Chen J, Chen J F, Tao R, Jiang J L, Hu Y, Xu J S, Zhang T Z, Liao J S. Plasmon catalytic PATP coupling reaction on Ag-NPs/graphite studied via in situ electrochemical surface-enhanced Raman spectroscopy[J]. Phys. Chem. Chem. Phys., 2020, 22(41): 23482-23490. https://doi.org/10.1039/d0cp01733g.

[15]

Zhao L B, Huang Y F, Wu D Y, Ren B. Surface-enhanced Raman spectroscopy and plasmon-assisted photocatalysis of p-aminothiophenol[J]. Acta Chim. Sin., 2014, 72(11): 1125-1138. https://doi.org/10.6023/A14080602.

[16]

Hu Y W, Yang T, Li Q H, Guan Q, Jiao K. Conjugated self-doped polyaniline-DNA hybrid as trigger for highly sensitive reagentless and electrochemical self-signal amplifying DNA hybridization sensing[J]. Analyst, 2013, 138(4): 1067-1074. https://doi.org/10.1039/c2an36620g.

[17]

Chu Q, Han B, Jin Y, Guo S, Jin S, Park E, Chen L, Jung Y M. Surface plasmon resonance induced charge transfer effect on the Ag-ZnSe-PATP system[J]. Spectrochim. Acta A, 2021, 248: 119167. https://doi.org/10.1016/j.saa.2020.119167.

[18]

Mao Z, Song W, Chen L, Ji W, Xue X X, Ruan W D, Li Z S, Mao H J, Ma S, Lombardi J R, Zhao B. Metal-semiconductor contacts induce the charge-transfer mechanism of surface-enhanced Raman scattering[J]. J. Phys. Chem. C, 2011, 115(37): 18378-18383. https://doi.org/10.1021/jp206455a.

[19]

Wang Y, Liu Y C, Ren C Y, Ma R F, Xu Z R, Zhao B. A charge-transfer-induced strategy for enantioselective discrimination by potential-regulated surface-enhanced Raman scattering spectroscopy[J]. Biosensors, 2023, 13(4): 471. https://doi.org/10.3390/bios13040471.

[20]

Sun M T, Xu H X. A novel application of plasmonics: Plasmon-driven surface-catalyzed reactions[J]. Small, 2012, 8(18): 2777-2786. https://doi.org/10.1002/smll.201200572.

[21]

Zhang M, Wang R, Cai Z Y, Zong C, Qiao H T, Wu D Y, Tian Z Q. Electrochemical surface-enhanced Raman spectroscopy for energy modulation of surface plasmon-mediated photoelectrochemical reactions of para-aminothiophenol on silver nanoparticle-modified electrodes[J]. J. Phys. Chem. C, 2023, 127(46): 22590-22599. https://doi.org/10.1021/acs.jpcc.3c05178.

[22]

Peng H Y, Xiao Y H, Yu H H, Wang J Z, Lin J D, Devasenathipathy R, Liu J, Zou P H, Zhang M, Zhou J Z, Wu D Y, Tian Z Q. Electrochemical and plasmonic photochemical oxidation processes of para-aminothiophenol on a nanostructured gold electrode[J]. J. Phys. Chem. C, 2021, 125(45): 24849-24858. https://doi.org/10.1021/acs.jpcc.1c05928.

[23]

Richter A P, Lombardi J R, Zhao B. Size and wavelength dependence of the charge-transfer contributions to surface-enhanced Raman spectroscopy in Ag/PATP/ZnO junctions[J]. J. Phys. Chem. C, 2010, 114(3): 1610-1614. https://doi.org/10.1021/jp909772e.

[24]

Huang Y F, Zhu H P, Liu G K, Wu D Y, Ren B, Xu X, Tian Z Q. When the signal is not from the original molecule to be detected: Chemical transformation of para-aminothiophenol on Ag during the SERS measurement[J]. J. Am. Chem. Soc., 2010, 132(27): 9244-9246. https://doi.org/10.1021/ja101107z.

[25]

Canpean V, Astilean S. Temperature effect on the SERS signature of p-aminothiophenol: A new evidence for the production of p,p'-dimercaptoazobenzene on metallic nanostructures[J]. Spectrochim. Acta A, 2012, 96: 862-867. https://doi.org/10.1016/j.saa.2012.07.120.

[26]

Sun M, Huang Y, Xia L, Chen X, Xu H X. The pH-controlled plasmon-assisted surface photocatalysis reaction of 4-aminothiophenol to p,p'-dimercaptoazobenzene on Au, Ag, and Cu colloids[J]. J. Phys. Chem. C, 2011, 115(19): 9629-9636. https://doi.org/10.1021/jp201002v.

[27]

Ji W, Spegazzini N, Kitahama Y, Chen Y J, Zhao B, Ozaki Y. pH-response mechanism of p-aminobenzenethiol on Ag nanoparticles revealed by two-dimensional correlation surface-enhanced Raman scattering spectroscopy[J]. J. Phys. Chem. Lett., 2012, 3(21): 3204-3209. https://doi.org/10.1021/jz301428e.

[28]

Gabudean A, Biro D, Astilean S. Localized surface plasmon resonance (LSPR) and surface-enhanced Raman scattering (SERS) studies of 4-aminothiophenol adsorption on gold nanorods[J]. J. Mol. Struct., 2011, 993(1-3): 420-424. https://doi.org/10.1016/j.molstruc.2010.11.045.

[29]

Zhan C, Wang Z Y, Zhang X G, Chen X J, Huang Y F, Hu S, Li J F, Wu D Y, Moskovits M, Tian Z Q. Interfacial construction of plasmonic nanostructures for the utilization of the plasmon-excited electrons and holes[J]. J. Am. Chem. Soc., 2019, 141(20): 8053-8057. https://doi.org/10.1021/jacs.9b02518.

[30]

Sun R, Li S J, Yao J L, Gu R A. Surface enhanced Raman spectroscopy and theoretical studies on the electrochemical transformation processes of 4-aminothiophenol on Au electrode[J]. Acta Chim. Sin., 2007, 65(17): 1741-1745.

[31]

Gao Y G, Yang N, You T T, Jiang L, Yin P G. Ultra-thin Au tip structure: a novel SERS substrate for in situ observation of a p-aminothiophenol surface-catalytic reaction[J]. RSC Adv., 2017, 7(8): 4541-4546. https://doi.org/10.1039/c6ra27799c.

[32]

Raj C R, Kitamura F, Ohsaka T. Electrochemical and in situ FTIR spectroscopic investigation on the electrochemical transformation of 4-aminothiophenol on a gold electrode in neutral solution[J]. Langmuir, 2001, 17(23): 7378-7386. https://doi.org/10.1021/la010746q.

[33]

Lukkari J. Electrochemical post-self-assembly transformation of 4-aminothiophenol monolayers on gold electrodes[J]. Langmuir, 1998, 14(8): 1705-1715. https://doi.org/10.1021/la970931x.

[34]

Fang Y, Li Y, Xu H X, Sun M. Ascertaining p,p'-dimercaptoazobenzene produced from p-aminothiophenol by selective catalytic coupling reaction on silver nanoparticles[J]. Langmuir, 2010, 26(11): 7737-7746. https://doi.org/10.1021/la904479q.

[35]

Zhang Z, Merk V, Hermanns A, Unger W E, Kneipp J. Role of metal cations in plasmon-catalyzed oxidation: A case study of p-aminothiophenol dimerization[J]. ACS Catal., 2017, 7(11): 7803-7809. https://doi.org/10.1021/acscatal.7b02700.

[36]

da Silva A G, Rodrigues T S, Correia V G, Alves T V, Alves R S, Ando R A, Ornellas F R, Wang J, Andrade L H, Camargo P H. Plasmonic nanorattles as next-generation catalysts for surface plasmon resonance-mediated oxidations promoted by activated oxygen[J]. Angew. Chem. Int. Ed., 2016, 55(25): 7111-7115. https://doi.org/10.1002/anie.201601740.

[37]

Tan Z, Li K X, Mao B W, Yan J W. Electrochemical scanning tunneling microscopy: Taking the initial stage of Cu electrodeposition on Au(111) as an example[J]. J. Electrochem., 2023, 29(7): 2216003. https://doi.org/10.13208/j.electrochem.2216003.

[38]

Yin X T, Wang W W, Tan Z, Ding Y, Mao B W, Yan J W. In situ SPM studies of electrochemical interfaces in high ionic strength electrolytes[J]. Curr. Opin. Electrochem., 2024, 47: 101563. https://doi.org/10.1016/j.coelec.2024.101563.

[39]

Tan Z, Li K, Gu Y, Nan Z, Wang W W, Sun L, Mao B W, Yan J W. Unconventional electrochemical behaviors of Cu underpotential deposition in a chloride-based deep eutectic solvent: High underpotential shift and low coverage[J]. Anal. Chem., 2023, 95(15): 6458-6466. https://doi.org/10.1021/acs.analchem.3c00637.

[40]

Tan Z, Li K, Xiao Y H, Gu Y, Nan Z, Wang W W, Sun L, Wu D Y, Mao B W, Yan J W. Electrochemical interfaces between Au(100) and deep eutectic solvents: An in situ scanning tunneling microscopy study[J]. Electrochim. Acta, 2023, 461: 142686. https://doi.org/10.1016/j.electacta.2023.142686.

[41]

Liang Y, Pfisterer J H, McLaughlin D, Csoklich C, Seidl L, Bandarenka A S, Schneider O. Electrochemical scanning probe microscopies in electrocatalysis[J]. Small Methods, 2019, 3(8): 1800387. https://doi.org/10.1002/smtd.201800387.

[42]

Kim Y T, McCarley R L, Bard A J. Scanning tunneling microscopy studies of gold (111) derivatized with organothiols[J]. J. Phys. Chem., 1992, 96(18): 7416-7421. https://doi.org/10.1021/j100197a052.

[43]

Batz V, Schneeweiss M A, Kramer D, Hagenström H, Kolb D M, Mandler D. Electrochemistry and structure of the isomers of aminothiophenol adsorbed on gold[J]. J. Electroanal. Chem., 2000, 491(1-2): 55-68. https://doi.org/10.1016/S0022-0728(00)00294-1.

[44]

Vericat C, Vela M E, Benitez G, Carro P, Salvarezza R C. Self-assembled monolayers of thiols and dithiols on gold: New challenges for a well-known system[J]. Chem. Soc. Rev., 2010, 39(5): 1805-1835. https://doi.org/10.1039/b907301a.

[45]

Sun J J, Su H S, Yue H L, Huang S C, Huang T X, Hu S, Sartin M M, Cheng J, Ren B. Role of adsorption orientation in surface plasmon-driven coupling reactions studied by tip-enhanced Raman spectroscopy[J]. J. Phys. Chem. Lett., 2019, 10(10): 2306-2312. https://doi.org/10.1021/acs.jpclett.9b00203.

[46]

Shao F, Zheng L Q, Lan J G, Zenobi R. Nanoscale chemical imaging of coadsorbed thiolate self-assembled monolayers on Au(111) by tip-enhanced Raman spectroscopy[J]. Anal. Chem., 2022, 94(3): 1645-1653. https://doi.org/10.1021/acs.analchem.1c03968.

[47]

Clavilier J, Faure R, Guinet G, Durand R. Preparation of monocrystalline Pt microelectrodes and electrochemical study of the plane surfaces cut in the direction of the {111} and {110} planes[J]. J. Electroanal. Chem. Interfacial Electrochem., 1980, 107(1): 205-209. https://doi.org/10.1016/S0022-0728(79)80022-4.

[48]

Delley B. An all-electron numerical method for solving the local density functional for polyatomic molecules[J]. J. Chem. Phys., 1990, 92(1): 508-517. https://doi.org/10.1063/1.458452.

[49]

Delley B. Fast calculation of electrostatics in crystals and large molecules[J]. J. Phys. Chem., 1996, 100(15): 6107-6110. https://doi.org/10.1021/jp952713n.

[50]

Perdew J P, Burke K, Ernzerhof M. Generalized gradient approximation made simple[J]. Phys. Rev. Lett., 1996, 77(18): 3865-3868. https://doi.org/10.1103/PhysRevLett.77.3865.

[51]

Schneeweiss M A, Kolb D M, Liu D, Mandler D. Anodic oxidation of Au(111)[J]. Can. J. Chem., 1997, 75(11): 1703-1709. https://doi.org/10.1139/v97-603.

[52]

Huang Y F, Zhang M, Zhao L B, Feng J M, Wu D Y, Ren B, Tian Z Q. Activation of oxygen on gold and silver nanoparticles assisted by surface plasmon resonances[J]. Angew. Chem. Int. Ed., 2014, 53(9): 2353-2357. https://doi.org/10.1002/anie.201310097.

[53]

Hill W, Wehling B. Potential- and pH-dependent surface-enhanced Raman scattering of p-mercaptoaniline on silver and gold substrates[J]. J. Phys. Chem., 1993, 97(37): 9451-9455. https://doi.org/10.1021/j100139a032.

[54]

Kim K, Kim K L, Shin D, Choi J Y, Shin K S. Surface-enhanced Raman scattering of 4-aminobenzenethiol on Ag and Au: pH dependence of b2-type bands[J]. J. Phys. Chem. C, 2012, 116(7): 4774-4779. https://doi.org/10.1021/jp211730r.

[55]

Hermann J M, Abdelrahman A, Jacob T, Kibler L A. Potential-dependent reconstruction kinetics probed by HER on Au(111) electrodes[J]. Electrochim. Acta, 2020, 347: 136287. https://doi.org/10.1016/j.electacta.2020.136287.

[56]

Pathaneni S S, Desiraju G R. Database analysis of Au⋯Au interactions[J]. J. Chem. Soc., Dalton Trans., 1993, 22(2): 319-322. https://doi.org/10.1039/DT9930000319.

[57]

Lavrich D J, Wetterer S M, Bernasek S L, Scoles G. Physisorption and chemisorption of alkanethiols and alkyl sulfides on Au(111)[J]. J. Phys. Chem. B, 1998, 102(18): 3456-3465. https://doi.org/10.1021/jp980047v.

[58]

Tao Y T, Wu C C, Eu J Y, Lin W L, Wu K C, Chen C H. Structure evolution of aromatic-derivatized thiol monolayers on evaporated gold[J]. Langmuir, 1997, 13(15): 4018-4023. https://doi.org/10.1021/la9700984.

[59]

Sabatan E, Cohen-Boulakia J, Bruening M, Rubinstein I. Thioaromatic monolayers on gold: A new family of self-assembling monolayers[J]. Langmuir, 1993, 9(11): 2974-2981. https://doi.org/10.1021/la00035a040.

[60]

Lang X, Liang Y, Liu S, Zhao S, Lau W M. Theoretical study of coupling p-aminothiophenol to hydroazo- and azo-adducts on Au(111)[J]. J. Mol. Model., 2016, 22: 197. https://doi.org/10.1007/s00894-016-3068-z.

PDF (7190KB)

189

Accesses

0

Citation

Detail

Sections
Recommended

/