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In situ redox strategy for large-scale fabrication of surfactant-free M-Fe_2O_3(M=Pt,Pd,Au) hybrid nanospheres 被引量:1

利用原位氧化还原策略宏量制备M-Fe_2O_3(M=Pt,Pd,Au)杂化纳米球(英文)
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摘要 A facile in situ redox strategy has been developed to fabricate surfactant-free M-Fe_2O_3(M = Pt, Pd, Au) hybrid nanospheres. In this process, noble metal salts were directly reduced by the pre-prepared Fe_3O_4 components in an alkaline aqueous solution without using organic reductants and surfactants. During the redox reaction, Fe_3O_4 was oxidized into Fe_2O_3,and the reduzates of noble metal nanoparticles were deposited on the surface of the Fe_2O_3 nanospheres. Then the characterizations were discussed in detail to study the formation of M-Fe_2O_3 hybrids. At last, catalytic CO oxidation was selected as a model reaction to evaluate the catalytic performance of these samples.It demonstrates that Pt-Fe_2O_3 nanospheres can catalyze 100 % conversion of CO into CO_2 at 90°C, indicating superior activity relative to Pd-Fe_2O_3 and Au-Fe_2O_3. 本工作利用原位氧化还原策略,成功制备出无表面活性剂修饰的M-Fe_2O_3(M=Pt,Pd,Au)杂化纳米球.在反应过程中,以事先制备好的Fe_3O_4纳米球作为载体和还原剂,在碱性条件下直接还原高价态的贵金属盐前躯体.反应后,Fe_3O_4被氧化成Fe_2O_3,而贵金属纳米粒子作为还原产物则牢牢的沉积在氧化产物Fe_2O_3表面形成M-Fe_2O_3杂化纳米球.通过表征系统研究了所得产物的形貌、结构和催化性质.并以CO催化氧化为模型反应对产物进行评估,结果表明,样品Pt-Fe_2O_3在90°C即可将CO 100%催化转化为CO_2,相比Pd-Fe_2O_3和Au-Fe_2O_3具有更高的催化活性.
出处 《Science China Materials》 SCIE EI CSCD 2016年第3期191-199,共9页 中国科学(材料科学(英文版)
基金 supported by the Fundamental Research Funds for the Central Universities the National Natural Science Foundation of China(51272249,51372007 and 21301014) the China Postdoctoral Science Foundation funded project
关键词 NOBLE metal iron OXIDES HYBRID CO oxidation NANOSPHERES noble metal iron oxides hybrid CO oxidation nanospheres
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