Molecular Cobalt Pentapyridine Catalysts for Generating Hydrogen from Water

被引:387
|
作者
Sun, Yujie [1 ,3 ]
Bigi, Julian P. [1 ,3 ]
Piro, Nicholas A. [1 ,3 ]
Tang, Ming Lee [1 ,4 ]
Long, Jeffrey R. [1 ,4 ]
Chang, Christopher J. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
基金
美国国家科学基金会;
关键词
FERRIC METHOXIDE COMPLEX; IRON-ONLY HYDROGENASE; RATE-DETERMINING STEP; H BOND ACTIVATION; ACTIVE-SITE; LOW OVERPOTENTIALS; ELECTROCATALYSTS; REDUCTION; MECHANISM; EVOLUTION;
D O I
10.1021/ja202743r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A set of robust molecular cobalt catalysts for the generation of hydrogen from water is reported. The cobalt complex supported by the parent pentadentate polypyridyl ligand PY5Me(2) features high stability and activity and 100% Faradaic efficiency for the electrocatalytic production of hydrogen from neutral water, with a turnover number reaching 5.5 x 10(4) mol of H(2) per mole of catalyst with no loss in activity over 60 h. Control experiments establish that simple Co(II) salts, the free PYSMe(2) ligand, and an isostructural PY5Me(2) complex containing redox-inactive Zn(II) are all ineffective for this reaction. Further experiments demonstrate that the overpotential for H(2) evolution can be tuned by systematic substitutions on the ancillary PYSMe(2) scaffold, presaging opportunities to further optimize this first-generation platform by molecular design.
引用
收藏
页码:9212 / 9215
页数:4
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