Electrocatalytic Multielectron Nitrite Reduction in Water by an Iron Complex

被引:47
|
作者
Stroka, Jesse R. [1 ]
Kandemir, Banu [1 ]
Matson, Ellen M. [1 ]
Bren, Kara L. [1 ]
机构
[1] Univ Rochester, Dept Chem, Rochester, NY 14627 USA
关键词
ammonia synthesis; electrocatalysis; hydroxylamine disproportionation; hydroxylamine synthesis; nitrite reductase; QUINQUEDENTATE MACROCYCLIC LIGANDS; METAL-COMPLEXES; MOLECULAR-STRUCTURES; 7-COORDINATION; CRYSTAL;
D O I
10.1021/acscatal.0c03600
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Catalytic reduction of nitrite by an iron complex in water near neutral pH to form hydroxylamine and ammonium is reported. The catalyst is an iron center coordinated by the pentadentate macrocycle 2,13-dimethyl-3,6,9,12,18-pentaazabicyclo[12.3.1]octadeca-1(18),2,12,14,16-pentaene (FeN5H2). Catalysis is observed by cyclic voltammetry at a half-wave potential of E-p/2 = -0.98 V vs Ag/AgCl (1 M KCl) when FeN5H2, nitrite, and a buffer (pH 7.2) are present. Controlled potential electrolysis of FeN5H2 and nitrite in pH 7.2 buffer at -0.98 V produces hydroxylamine (faradaic efficiency > 90%). FeN5H2 catalyzes ammonium production by disproportionation of hydroxylamine with concomitant formation of nitrous oxide and These results are a rare example of multielectron clectrocatalytic nitrite reduction by an iron complex near neutral pH.
引用
收藏
页码:13968 / 13972
页数:5
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