Longitudinal Strain Engineering of Cu2-xS by the Juxtaposed Cu5FeS4 Phase in the Cu5FeS4/Cu2-xS/Cu5FeS4 Nanosandwich

被引：18

作者：

Park, Jongsik ^{[1
,2
]}

Lim, Sunghyun ^{[1
,2
]}

Kwon, Taehyun ^{[1
,2
]}

Jun, Minki ^{[1
,2
]}

Oh, Aram ^{[1
,2
,3
]}

Baik, Hionsuck ^{[3
]}

Lee, Kwangyeol ^{[1
,2
]}

机构：

[1] Korea Univ, Dept Chem, Seoul 02841, South Korea

[2] Korea Univ, Res Inst Nat Sci, Seoul 02841, South Korea

[3] KBSI, Seoul 02841, South Korea

来源：

CHEMISTRY OF MATERIALS | 2019年 / 31卷 / 21期

关键词：

SHAPE-CONTROLLED SYNTHESIS; SELECTIVE CATION-EXCHANGE; TRANSFORMATIONS; NANOCRYSTALS; NANOSCALE; REDUCTION; TEMPLATES; HYDROGEN; ANION; WATER;

D O I：

10.1021/acs.chemmater.9b03342

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：

Structurally well-defined heteronanoparticles have received great attention because their distinct structural features can be altered to achieve unprecedented properties. The cation exchange reaction, one of the most powerful techniques to synthesize heteronanoparticles, can tune the regiospecific composition of nanoparticles while maintaining the overall morphology of the template. Herein, we demonstrate that the nascent interface between the cation-exchanged region and the unchanged template can induce a significant tensile or compressive strain on the lattice of the template so that the cation exchange process at the interface can be greatly facilitated. The fate of the overall cation exchange reaction can be dictated by placing the initial cation exchange sites on the template regioselectively. Via a careful kinetic and thermodynamic control of the cation exchange, we could prepare two completely different nanostructures of Cu5FeS4/Cu2-xS/Cu5FeS4 nanosandwich andCu(5)FeS(4)/Cu2-xS Janus nanoparticle. The synthetic concept described in this study could be further extended to the synthesis of various rationally designed multiphasic nanoparticles with exciting physicochemical properties.

引用

页码：9070 / 9077

页数：8

共 43 条

[41] Lattice Strain and Ligand Effects on the Formation of Cu2-xS/I-III-VI2 Nanorod Heterostructures through Partial Cation Exchange [J].