物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2015年
4期
764-770
,共7页
李宪华%张雷刚%王雪雪%于清波
李憲華%張雷剛%王雪雪%于清波
리헌화%장뢰강%왕설설%우청파
热稳定性%PANI/g-C3N4%催化性能
熱穩定性%PANI/g-C3N4%催化性能
열은정성%PANI/g-C3N4%최화성능
Thermal stability%PANI/g-C3N4%Photocatalytic activity
利用界面聚合法,成功将聚苯胺(PANI)纳米棒生长在石墨型氮化碳(g-C3N4)片层上,制备了PANI/g-C3N4复合光催化剂。采用傅里叶变换红外(FTIR)光谱、X射线衍射(XRD)、扫描电镜(SEM)、紫外-可见(UV-Vis)光谱、热重分析(TGA)和电化学工作站表征手段考察样品的结构、形貌及性能,以可见光催化降解亚甲基蓝为模型考察样品的可见光催化活性。实验结果表明,在复合材料中的g-C3N4能很好地分散成层状,并在层间与PANI纳米棒形成复合物,这种特殊的复合结构不仅利于片状g-C3N4对PANI链段运动的限制及对其降解产物的物理屏蔽,从而可以提高复合材料的热稳定性,而且具有优越的可见光催化性能。
利用界麵聚閤法,成功將聚苯胺(PANI)納米棒生長在石墨型氮化碳(g-C3N4)片層上,製備瞭PANI/g-C3N4複閤光催化劑。採用傅裏葉變換紅外(FTIR)光譜、X射線衍射(XRD)、掃描電鏡(SEM)、紫外-可見(UV-Vis)光譜、熱重分析(TGA)和電化學工作站錶徵手段攷察樣品的結構、形貌及性能,以可見光催化降解亞甲基藍為模型攷察樣品的可見光催化活性。實驗結果錶明,在複閤材料中的g-C3N4能很好地分散成層狀,併在層間與PANI納米棒形成複閤物,這種特殊的複閤結構不僅利于片狀g-C3N4對PANI鏈段運動的限製及對其降解產物的物理屏蔽,從而可以提高複閤材料的熱穩定性,而且具有優越的可見光催化性能。
이용계면취합법,성공장취분알(PANI)납미봉생장재석묵형담화탄(g-C3N4)편층상,제비료PANI/g-C3N4복합광최화제。채용부리협변환홍외(FTIR)광보、X사선연사(XRD)、소묘전경(SEM)、자외-가견(UV-Vis)광보、열중분석(TGA)화전화학공작참표정수단고찰양품적결구、형모급성능,이가견광최화강해아갑기람위모형고찰양품적가견광최화활성。실험결과표명,재복합재료중적g-C3N4능흔호지분산성층상,병재층간여PANI납미봉형성복합물,저충특수적복합결구불부리우편상g-C3N4대PANI련단운동적한제급대기강해산물적물리병폐,종이가이제고복합재료적열은정성,이차구유우월적가견광최화성능。
Polyaniline (PANI) nanorods grown on layered graphitic carbon nitride (g-C3N4) sheets are synthesized by interfacial polymerization. The structure, morphology, and properties of the photocatalysts are characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), and UV-visible (UV-Vis) spectroscopies, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and electrochemical analysis. Photocatalytic degradation of methylene blue is investigated to determine the photoactivity of the catalyst. The results suggest that g-C3N4 possesses good dispersion with an intercalated nanostructure and interfacial adhesion with PANI. In addition, the PANI/g-C3N4 composites retain the advantage of high thermal stability resident with g-C3N4. This is ascribed to a physical barrier effect on the emanation of degradation products and inhibited polymer motion. The resulting composites also show more intensive photocatalytic activity than does g-C3N4.