We have prepared self-assembled monolayers (SAMs) of 4-aminothiophenol (4-ATP) and 1-(4-mercaptophenyl)-2,6-diphenyl-4-(4-pyridyl)pyridinium tetrafluoroborate (MDPP) functionalized with iron phthalocyanine (FePc) and copper phthalocyanine (CuPc) adsorbed on gold (111) electrodes. The catalytic activity of these SAMs/MPc was examined for the reduction of O 2 in aqueous solutions and compared to that of bare gold and with gold coated directly with preadsorbed MPc molecules. Scanning tunneling microscopy (STM) studies confirm the functionalization of the 4-ATP by MPc. STM images reveal that iron phthalocyanine molecules are chemically anchored to 4-aminothiophenol organic monolayers, probably having an "umbrella" type orientation with regards to the surface. The electrocatalytic studies carried out with Au/4-ATP/FePc and Au/ MDPP/FePc electrodes show that the O 2 reduction takes place by the transfer of 4-electron to give water in contrast to a 2-electron transfer process observed for the bare gold. The modified electrode obtained by simple adsorption of FePc directly to the Au(111) surface still promotes the 4-electron reduction process, but it shows a lower activity than the electrodes involving SAMs with FePc molecules positioned at the outmost portion of the selfassembled monolayers. The activity of the electrodes increases as follow: Au < Au/FePc < Au/4-ATP/FePc < Au/MDPP/FePc with the highest activity when FePc molecules are more separated from the Au surface. In contrast, the less active CuPc shows almost the same activity in all three configurations. Theoretical calculations suggest the importance of the back-bonding into the adduct formation, showing the relevance of the supporting gold surface on the electron-transfer process mediated by anchoring ligands.
We
have been able to “tune” the electrocatalytic
activity of iron phthalocyanine (FePc) and iron hexadodecachlorophthalocyanine
(16(Cl)FePc) for the oxygen reduction reaction (ORR) by manipulating
the “pull effect” of pyridinium molecules axially bounded
to the phthalocyanine complexes (FePcs). These axial ligands play
both the role of molecular anchors and also of molecular wires. The
axial ligands also affect the reactivity of the Fe metal center in
the phthalocyanine. The “pull effect” originates from
the positive charge located on the pyridinium core. We have explored
the influence of the core positions (Up or Down), in two structural
pyridiniums isomers on the activity of FePc and 16(Cl)FePc for the
ORR. Of all self-assembled catalysts tested, the highest catalytic
activity was exhibited by the Au(111)/Up/FePc system. XPS measurements
and DFT calculations showed that it is possible to tailor the FePc–N(pyridiniums)
Fe–O2 binding energies, by changing the core positions
and affecting the “pull effect” of pyridiniums. This
affects directly the catalytic activity of FePcs. The plot of activity
as (log I)E versus the calculated Fe–O2 binding energies gives an activity volcano correlation, indicating
that an optimum binding energy of O2 with the Fe center
provides the highest activity.
The formation of self-assembly monolayers (SAMs) based on a gold substrate and a thiolate ligand as "anchor" fragment of metallophtalocyanine has been employed as strategy toward the obtention of modified electrodes. In this Article, the formation of SAM's involving iron and cobalt phtalocyanines anchored by 4-aminothiophenol (4-ATP) and 4-mercatopyridine (4-MP) to the Au(111) surface is explored by both experimental and theoretical studies for a better understanding of their bonding pattern and optical properties. The self-assembly metallophthalocyanines complexes on gold electrode exhibits an interesting charge donation from the 4-ATP or 4-MP toward both gold substrate and phtalocyanine, denoting an effective goldÀMPc interaction mediated by the titled anchor ligands. In addition, the optical properties of the self-assembled complexes supported on the gold electrode exhibit in conjuction with the well-described Q-band an interesting charge transfer from the Pc (π) toward the gold surface, as could be observed in the FePc-4MP-Au 26 assembly.
A redox catalyst can be present in the solution phase or immobilized on the electrode surface. When the catalyst is present in the solution phase the process can proceed via inner-(with bond formation, chemical catalysis) or outer-sphere mechanisms (without bond formation, redox catalysis). For the latter, log k is linearly proportional to the redox potential of the catalysts, E°. In contrast, for inner-sphere catalyst, the values of k are much higher than those predicted by the redox potential of the catalyst. The behaviour of these catalysts when they are confined on the electrode surface is completely different. They all seem to work as inner-sphere catalysts where a crucial step is the formation of a bond between the active site and the target molecule. Plots of (log i) E versus E°give linear or volcano correlations. What is interesting in these volcano correlations is that the falling region corresponding to strong adsorption of intermediates to the active sites is not necessarily attributed to a gradual surface occupation of active sites by intermediates (Langmuir isotherm) but rather to a gradual decrease in the amount of M(II) active sites which are transformed into M(III)OH inactive sites due to the applied potential.
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