A remote-controlled generation of gold@polydopamine (core@shell) nanoparticles via physical-chemical stimuli of polydopamine/gold composites

被引:30
|
作者
Lee, Yi Seul [1 ]
Bae, Ji Young [1 ]
Koo, Hye Young [2 ]
Lee, Young Boo [3 ]
Choi, Won San [1 ]
机构
[1] Hanbat Natl Univ, Dept Chem & Biol Engn, 125 Dongseodaero, Daejeon 305719, South Korea
[2] Korea Inst Sci & Technol, Jeonbuk Inst Adv Composite Mat, 92 Chudong Ro, Wanju Gun, Jeollabuk Do, South Korea
[3] Korea Basic Sci Inst, Jeonju Ctr, Dukjin Dong 1 Ga, Jeonju 561756, South Korea
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
新加坡国家研究基金会;
关键词
EFFICIENT; BIOCOMPATIBILITY; FABRICATION; ADSORPTION; CHEMISTRY; CATALYSTS; SURFACES; SPHERES; FILMS;
D O I
10.1038/srep22650
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We present the synthesis of polydopamine particle-gold composites (PdopP-Au) and unique release of Au@Pdop core@shell nanoparticles (NPs) from the PdopP-Au upon external stimuli. The PdopP-Au was prepared by controlled synthesis of AuNPs on the Pdop particles. Upon near infrared (NIR) irradiation or NaBH4 treatment on the PdopP-Au, the synthesized AuNPs within the PdopPs could be burst-released as a form of Au@Pdop NPs. The PdopP-Au composite showed outstanding photothermal conversion ability under NIR irradiation due to the ultrahigh loading of the AuNPs within the PdopPs, leading to a remote-controlled explosion of the PdopP-Au and rapid formation of numerous Au@Pdop NPs. The release of the Au@Pdop NPs could be instantly stopped or re-started by off or reboot of NIR, respectively. The structure of the released Au@Pdop NPs is suitable for a catalyst or adsorbent, thus we demonstrated that the PdopP-Au composite exhibited excellent and sustained performances for environmental remediation due to its capability of the continuous production of fresh catalysts or adsorbents during the reuse.
引用
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页数:11
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