4.8 Article

Defining Rules for the Shape Evolution of Gold Nanoparticles

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 35, 页码 14542-14554

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ja305245g

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资金

  1. AFOSR [FA9550-11-1-0275, FA9550-09-1-0294]
  2. DoD/NSSEFF/NPS [N00244-09-1-0012]
  3. Non-equilibrium Energy Research Center (NERC) DOE Award [DE-SC0000989]
  4. Nanoscale Science and Engineering Initiative NSF Award [EEC-0647560]
  5. NSF MRSEC [DMR-0520513, DMR-1121262]
  6. NSF-NSEC
  7. NSF-MRSEC
  8. Keck Foundation
  9. state of Illinois
  10. Northwestern University (NU)
  11. DoD through the National Defense Science & Engineering Graduate (NDSEG) [32 CFR 168a]
  12. Division Of Materials Research
  13. Direct For Mathematical & Physical Scien [1121262] Funding Source: National Science Foundation

向作者/读者索取更多资源

The roles of silver ions and halides (chloride, bromide, and iodide) in the seed-mediated synthesis of gold nanostructures have been investigated, and their influence on the growth of 10 classes of nanoparticles that differ in shape has been determined. We systematically studied the effects that each chemical component has on the particle shape, on the rate of particle formation, and on the chemical composition of the particle surface. We demonstrate that halides can be used to (1) adjust the reduction potential of the gold ion species in solution and (2) passivate the gold nanoparticle surface, both of which control the reaction kinetics and thus enable the selective synthesis of a series of different particle shapes. We also show that silver ions can be used as an underpotential deposition agent to access a different set of particle shapes by controlling growth of the resulting gold nanoparticles through surface passivation (more so than kinetic effects). Importantly, we show that the density of silver coverage can be controlled by the amount and type of halide present in solution. This behavior arises from the decreasing stability of the underpotentially deposited silver layer in the presence of larger halides due to the relative strengths of the Ag+/Ag-0-halide and Au+/Au-0-halide interactions, as well as the passivation effects of the halides on the gold particle surface. We summarize this work by proposing a set of design considerations for controlling the growth and final shape of gold nanoparticles prepared by seed-mediated syntheses through the judicious use of halides and silver ions.

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