功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
19期
19115-19120
,共6页
水热法%Zn1 -x Cox Ga2 O 4%光催化%罗丹明 B
水熱法%Zn1 -x Cox Ga2 O 4%光催化%囉丹明 B
수열법%Zn1 -x Cox Ga2 O 4%광최화%라단명 B
hydrothermal method%Zn1 -x Cox Ga2 O4%photocatalytic%Rhodamine B
以ZnCl2、Ga(NO3)3??xH2O、CoCl2??6H2O为原料,采用水热法制备了立方晶型的Zn1-xCoxGa2O4光催化剂,用X射线衍射(XRD)、扫描电子显微镜(SEM)、紫外漫反射(UV-Vis)、X射线光电子能谱(XPS)等测试手段对催化剂进行了表征,结果表明, Co成功地掺入到ZnGa2O4晶格内, Co的掺入能够影响催化剂的形貌,缩小催化剂的禁带宽度.光催化降解罗丹明B溶液实验结果表明, Co的掺入提高了催化剂的催化活性,掺入量为x=0.010的Zn1-xCoxGa2O4具有最佳的光催化性能,同时Zn1-xCoxGa2O4样品对罗丹明B溶液的光催化降解反应符合伪一级反应动力学规律.并对Co掺入后光催化活性提高的机理进行了讨论.
以ZnCl2、Ga(NO3)3??xH2O、CoCl2??6H2O為原料,採用水熱法製備瞭立方晶型的Zn1-xCoxGa2O4光催化劑,用X射線衍射(XRD)、掃描電子顯微鏡(SEM)、紫外漫反射(UV-Vis)、X射線光電子能譜(XPS)等測試手段對催化劑進行瞭錶徵,結果錶明, Co成功地摻入到ZnGa2O4晶格內, Co的摻入能夠影響催化劑的形貌,縮小催化劑的禁帶寬度.光催化降解囉丹明B溶液實驗結果錶明, Co的摻入提高瞭催化劑的催化活性,摻入量為x=0.010的Zn1-xCoxGa2O4具有最佳的光催化性能,同時Zn1-xCoxGa2O4樣品對囉丹明B溶液的光催化降解反應符閤偽一級反應動力學規律.併對Co摻入後光催化活性提高的機理進行瞭討論.
이ZnCl2、Ga(NO3)3??xH2O、CoCl2??6H2O위원료,채용수열법제비료립방정형적Zn1-xCoxGa2O4광최화제,용X사선연사(XRD)、소묘전자현미경(SEM)、자외만반사(UV-Vis)、X사선광전자능보(XPS)등측시수단대최화제진행료표정,결과표명, Co성공지참입도ZnGa2O4정격내, Co적참입능구영향최화제적형모,축소최화제적금대관도.광최화강해라단명B용액실험결과표명, Co적참입제고료최화제적최화활성,참입량위x=0.010적Zn1-xCoxGa2O4구유최가적광최화성능,동시Zn1-xCoxGa2O4양품대라단명B용액적광최화강해반응부합위일급반응동역학규률.병대Co참입후광최화활성제고적궤리진행료토론.
The cubic Zn1-xCoxGa2O4 photocatalysts were synthesized by hydrothermal method using ZnCl2, Ga(NO3)3??xH2O, CoCl2??6H2O as raw material. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), UV-Vis diffusion reflectance spectra (UV-Vis)and X-ray photoelectron spectroscope (XPS). The results indicate that the Co was successfully incorporated into the ZnGa2O4 lattice, and Co doping can influence the crystalline morphology and narrow the band gap of photocatalysts. The experi-ments of photocatalytic degradation of RhB results demonstrate that Co doping can greatly enhance the photo-catalytic activity of Zn1-xCoxGa2O4. When Co dopant was x=0.010, the photocatalytic activity reaches the maximum. Moreover, the photocatalytic degradation of RhB follows a pseudo-first-order reaction. The mecha-nism of enhanced photocatalytic activity was also discussed.