Environmental Stimuli-Irresponsive Long-Term Radical Scavenging of 2D Transition Metal Dichalcogenides through Defect-Mediated Hydrogen Atom Transfer in Aqueous Media

被引:14
|
作者
Kim, Ji Eun [1 ]
Yim, DaBin [2 ]
Lee, Chi Ho [1 ]
Jun, Byeongsun [1 ]
Nam, Jin [3 ]
Han, Sang Hoon [3 ]
Lee, Sang Uck [1 ,4 ]
Kim, Jong-Ho [2 ]
Kim, Jin Woong [1 ,4 ]
机构
[1] Hanyang Univ, Dept Bionano Technol, Ansan 15588, South Korea
[2] Hanyang Univ, Dept Chem Engn, Ansan 15588, South Korea
[3] Amore Pacific Co, R&D Ctr, Yongin 17074, South Korea
[4] Hanyang Univ, Dept Chem & Mol Engn, Ansan 15588, South Korea
基金
新加坡国家研究基金会;
关键词
amphiphilic block copolymers; hydrogen transfer; radical scavenging; transition metal dichalcogenide nanosheets; INITIO MOLECULAR-DYNAMICS; TOTAL-ENERGY CALCULATIONS; AUGMENTED-WAVE METHOD; ANTIOXIDANT ACTIVITY; 2-DIMENSIONAL MATERIALS; CANCER-THERAPY; DRUG-DELIVERY; BASIS-SET; MOS2; NANOSHEETS;
D O I
10.1002/adfm.201802737
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A transition metal dichalcogenide (TMD) based antioxidation platform is proposed, in which radical scavenging is accomplished by the defect-mediated one-step hydrogen atom transfer (HAT) occurring on the nanosheets in water. To this end, the TMD nanosheets, including MoS2, WS2, MoSe2, and WSe2, are finely dispersed in water with the aid of an amphiphilic poly(epsilon-caprolactone)-b-poly(ethylene oxide) (PCL-b-PEO) diblock copolymer that envelops the nanosheets with a molecular layer of less than 1 nm thickness. It is then demonstrated that the PCL-b-PEO-stabilized TMD nanosheets show the extraordinarily enhanced and prolonged radical scavenging activity in water even under harsh storage conditions. Theoretical modeling studies on HAT suggest that more favorable hydrogen association from chalcogen vacancies on the nanosheets dispersed in water can lead to the easier dissociation of hydrogen atoms with exothermicity by -0.43 to -1.33 eV, thus exhibiting such an outstanding radical scavenging performance.
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页数:8
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