Ligand effects on the stability of thiol-stabilized gold nanoclusters: Au25(SR)18-, Au38(SR)24, and Au102(SR)44

被引:109
作者
Jung, Jaehoon [2 ]
Kang, Sunwoo [1 ]
Han, Young-Kyu [1 ]
机构
[1] Korea Basic Sci Inst, Div Mat Sci, Taejon 305333, South Korea
[2] RIKEN, Adv Sci Inst, Wako, Saitama 3510198, Japan
基金
新加坡国家研究基金会;
关键词
AB-INITIO PSEUDOPOTENTIALS; ELECTRONIC-STRUCTURE; PROTECTED AU-38; CRYSTAL-STRUCTURE; TRANSITION; CLUSTERS; MODEL; NANOPARTICLE; MOLECULES; SOLIDS;
D O I
10.1039/c2nr30501a
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
We have studied the electrochemical and thermodynamic stability of Au-25(SR)(18)(-), Au-38(SR)(24), and Au-102(SR)(44), R = CH3, C6H13, CH2CH2Ph, Ph, PhF, and PhCOOH, in order to examine ligand effects on the stability of thiol-stabilized gold nanoclusters, Au-m(SR)(n). Aliphatic thiols, in general, have higher electrochemical and thermodynamic stability than aromatic thiols, and the -SCH2CH2Ph thiol is particularly appealing because of its high electrochemical and thermodynamic stability. The stabilization of Au-m by nSR for Au-m(SR)(n) can be rationalized by the stabilization of an Au atom by an SR for the simple molecule AuSR, regardless of interligand interaction and system size and shape. Thiol moieties play a strong role in the electron oxidation and reduction of Au-m(SR)(n). Accounting for the characteristics of thiol ligands is essential for understanding the electronic and thermodynamic stability of thiol-stabilized gold nanoclusters.
引用
收藏
页码:4206 / 4210
页数:5
相关论文
共 42 条
[1]
Geometric and Electronic Structure of Au25(SPhX)18- (X = H, F, Cl, Br, CH3, and OCH3) [J].
Aikens, Christine M. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2010, 1 (17) :2594-2599
[2]
On the structure of thiolate-protected Au25 [J].
Akola, Jaakko ;
Walter, Michael ;
Whetten, Robert L. ;
Haekkinen, Hannu ;
Groenbeck, Henrik .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (12) :3756-+
[3]
ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 2ND AND 3RD ROW TRANSITION-ELEMENTS [J].
ANDRAE, D ;
HAUSSERMANN, U ;
DOLG, M ;
STOLL, H ;
PREUSS, H .
THEORETICA CHIMICA ACTA, 1990, 77 (02) :123-141
[4]
Gold nanoelectrodes of varied size: Transition to molecule-like charging [J].
Chen, SW ;
Ingram, RS ;
Hostetler, MJ ;
Pietron, JJ ;
Murray, RW ;
Schaaff, TG ;
Khoury, JT ;
Alvarez, MM ;
Whetten, RL .
SCIENCE, 1998, 280 (5372) :2098-2101
[5]
Dass A., UNPUB
[6]
Nano-scaling law: geometric foundation of thiolated gold nanomolecules [J].
Dass, Amala .
NANOSCALE, 2012, 4 (07) :2260-2263
[7]
AN ALL-ELECTRON NUMERICAL-METHOD FOR SOLVING THE LOCAL DENSITY FUNCTIONAL FOR POLYATOMIC-MOLECULES [J].
DELLEY, B .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (01) :508-517
[8]
From molecules to solids with the DMol3 approach [J].
Delley, B .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (18) :7756-7764
[9]
ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 1ST-ROW TRANSITION-ELEMENTS [J].
DOLG, M ;
WEDIG, U ;
STOLL, H ;
PREUSS, H .
JOURNAL OF CHEMICAL PHYSICS, 1987, 86 (02) :866-872
[10]
Ab initio study of thiolate-protected Au102 nanocluster [J].
Gao, Yi ;
Shao, Nan ;
Zeng, Xiao Cheng .
ACS NANO, 2008, 2 (07) :1497-1503