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Pd 0 ‐ and Au 0 ‐Nanoparticles Catalyze the Reduction of Perchlorate by ·C(CH 3 ) 2 OH Radicals
Author(s) -
Benjamini Gadi,
BarZiv Ronen,
Zidki Tomer,
Borojovich Eitan J. C.,
Yardeni Guy,
Kornweitz Haya,
Meyerstein Dan
Publication year - 2017
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201700654
Subject(s) - chemistry , perchlorate , catalysis , radical , reducing agent , inorganic chemistry , palladium , aqueous solution , hydrogen , adsorption , colloidal gold , nanoparticle , photochemistry , organic chemistry , nanotechnology , ion , materials science
Catalytic water reduction to hydrogen takes place when metal nanoparticles (M 0 ‐NPs) of gold or palladium are charged with an excess of electrons by an electron‐transfer process from strong reducing α‐alcohol radicals such as · C(CH 3 ) 2 OH. The results reported in this study indicate that the M 0 ‐NPs also catalyze the reduction of perchlorate by · C(CH 3 ) 2 OH radicals and by BH 4 – . The results point out that the M 0 ‐NPs behave as nanoelectrodes. The catalytic reduction of perchlorate competes well with the catalytic reduction of water; that is, although the concentration of perchlorate is orders of magnitude smaller than that of water, the radicals reduce the perchlorate preferentially. Thus, we have identified a new way to deal with the residual perchlorate in water, using any reducing agent forming adsorbed hydrogen. The nature of the reactive reducing agent (M 0 ‐NPs) n – /{(M 0 ‐NPs) – H m } ( n – m )– [ n = number of excess electrons and m = number of electrons given off after the same number of H atoms have been adsorbed] and the energetic processes, which might be different for the two M 0 ‐NPs, are discussed. The results demonstrate that M 0 ‐NPs can be developed as simple and effective catalysts for the removal of perchlorate from polluted aqueous solutions.