催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2010年
1期
24-32
,共9页
马腾%傅强%崔义%张镇%王珍%谭大力%包信和
馬騰%傅彊%崔義%張鎮%王珍%譚大力%包信和
마등%부강%최의%장진%왕진%담대력%포신화
双金属催化剂%氧化物%Pt富集表面%反相模型体系
雙金屬催化劑%氧化物%Pt富集錶麵%反相模型體繫
쌍금속최화제%양화물%Pt부집표면%반상모형체계
bimetallic catalyst%oxide%platinum-skin%inverse model system
利用扫描隧道显微镜(STM)和X射线光电子能谱(XPS)对Pt(111)表面制备的Fe单层薄膜及其在不同环境气氛条件下的多种结构进行了研究.在温度为487K的Pt(111)表面制备出了完整的Fe单层薄膜Fe/Pt(111).对Fe/Pt(111)依次升高温度进行超高真空退火,STM和XPS结果表明退火温度高于800 K时,表面Fe原子扩散到次表层区域,形成次表层Fe结构Pt/Fe/Pt(111).Pt/Fe/Pt(111)在O_2氧化气氛中经850 K退火可转变成表面FeO薄膜FeO/Pt(111).FeO/Pt(111)结构在温和的H_2还原气氛中(600K)转变成表面Fe结构,进一步的还原处理(800K)则可以重新生成Pt/Fe/Pt(111).控制样品的环境气氛在O_2和H_2之间切换,使得表面Fe(FeO)和次表面Fe可以重复地转变.本研究实现了多种Fe-Pt表面结构的可控制备,可为合理地设计高效、价廉的催化剂提供借鉴.
利用掃描隧道顯微鏡(STM)和X射線光電子能譜(XPS)對Pt(111)錶麵製備的Fe單層薄膜及其在不同環境氣氛條件下的多種結構進行瞭研究.在溫度為487K的Pt(111)錶麵製備齣瞭完整的Fe單層薄膜Fe/Pt(111).對Fe/Pt(111)依次升高溫度進行超高真空退火,STM和XPS結果錶明退火溫度高于800 K時,錶麵Fe原子擴散到次錶層區域,形成次錶層Fe結構Pt/Fe/Pt(111).Pt/Fe/Pt(111)在O_2氧化氣氛中經850 K退火可轉變成錶麵FeO薄膜FeO/Pt(111).FeO/Pt(111)結構在溫和的H_2還原氣氛中(600K)轉變成錶麵Fe結構,進一步的還原處理(800K)則可以重新生成Pt/Fe/Pt(111).控製樣品的環境氣氛在O_2和H_2之間切換,使得錶麵Fe(FeO)和次錶麵Fe可以重複地轉變.本研究實現瞭多種Fe-Pt錶麵結構的可控製備,可為閤理地設計高效、價廉的催化劑提供藉鑒.
이용소묘수도현미경(STM)화X사선광전자능보(XPS)대Pt(111)표면제비적Fe단층박막급기재불동배경기분조건하적다충결구진행료연구.재온도위487K적Pt(111)표면제비출료완정적Fe단층박막Fe/Pt(111).대Fe/Pt(111)의차승고온도진행초고진공퇴화,STM화XPS결과표명퇴화온도고우800 K시,표면Fe원자확산도차표층구역,형성차표층Fe결구Pt/Fe/Pt(111).Pt/Fe/Pt(111)재O_2양화기분중경850 K퇴화가전변성표면FeO박막FeO/Pt(111).FeO/Pt(111)결구재온화적H_2환원기분중(600K)전변성표면Fe결구,진일보적환원처리(800K)칙가이중신생성Pt/Fe/Pt(111).공제양품적배경기분재O_2화H_2지간절환,사득표면Fe(FeO)화차표면Fe가이중복지전변.본연구실현료다충Fe-Pt표면결구적가공제비,가위합리지설계고효、개렴적최화제제공차감.
Monolayer Fe films on Pt(111) and their derived structures under different environments were investigated by scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). The growth of monolayer Fe films was seen at 487 K. The surface compo-sition and structure of the Fe/Pt(111) surface were monitored by XPS and STM during stepwise annealing under vacuum. Surface Fe was driven into the subsurface region during annealing above 800 K. This resulted in a Pt-skin surface of Pt/Fe/Pt(111). Oxidation of the Pt-skin structure in O_2 produced a FeO surface structure, FeO/Pt(111). This was transformed into a surface Fe structure by mild reduction in H_2 (600 K) and into subsurface Fe by further severe reduction (800 K). The transformation of surface Fe (FeO) and subsurface Fe in Pt(111) was reversible in cycled oxidation and reduction treatments. The results demonstrated the controlled preparation of various Fe-Pt surfaces. This can be important for the design of high-performance and low-cost catalysts.