陕西科技大学学报(自然科学版)
陝西科技大學學報(自然科學版)
협서과기대학학보(자연과학판)
JOURNAL OF SHAANXI UNIVERSITY OF SCIENCE & TECHNOLOGY
2014年
6期
61-66
,共6页
孔新刚%郭章林%黄剑锋%李嘉胤%介燕妮%孙有权
孔新剛%郭章林%黃劍鋒%李嘉胤%介燕妮%孫有權
공신강%곽장림%황검봉%리가윤%개연니%손유권
钽酸钠%复合相%水热%光催化
鐽痠鈉%複閤相%水熱%光催化
단산납%복합상%수열%광최화
sodium tantalate%composite%hydrothermal synthesis%photocatalysis
以六钽酸钠(Na8 Ta6 O19)为原料,采用水热法实现了烧绿石型 Na2 Ta2 O6、钙钛矿型NaTaO3以及Na2 Ta2 O6/NaTaO3复合光催化剂的可控合成。通过X射线衍射、场发射扫描电子显微镜、紫外‐可见漫反射光谱对样品进行了表征,研究了水热反应中碱浓度、溶剂类型、pH值等对钽酸钠晶体结构和形貌的影响。光催化降解亚甲基蓝结果表明,光催化降解活性顺序为Na2 Ta2 O6/NaTaO3>Na2 Ta2 O6>NaTaO3,复合相中Na2 Ta2 O6和NaTaO3之间形成了异质结,能够有效的抑制光生电子空穴对的复合。
以六鐽痠鈉(Na8 Ta6 O19)為原料,採用水熱法實現瞭燒綠石型 Na2 Ta2 O6、鈣鈦礦型NaTaO3以及Na2 Ta2 O6/NaTaO3複閤光催化劑的可控閤成。通過X射線衍射、場髮射掃描電子顯微鏡、紫外‐可見漫反射光譜對樣品進行瞭錶徵,研究瞭水熱反應中堿濃度、溶劑類型、pH值等對鐽痠鈉晶體結構和形貌的影響。光催化降解亞甲基藍結果錶明,光催化降解活性順序為Na2 Ta2 O6/NaTaO3>Na2 Ta2 O6>NaTaO3,複閤相中Na2 Ta2 O6和NaTaO3之間形成瞭異質結,能夠有效的抑製光生電子空穴對的複閤。
이륙단산납(Na8 Ta6 O19)위원료,채용수열법실현료소록석형 Na2 Ta2 O6、개태광형NaTaO3이급Na2 Ta2 O6/NaTaO3복합광최화제적가공합성。통과X사선연사、장발사소묘전자현미경、자외‐가견만반사광보대양품진행료표정,연구료수열반응중감농도、용제류형、pH치등대단산납정체결구화형모적영향。광최화강해아갑기람결과표명,광최화강해활성순서위Na2 Ta2 O6/NaTaO3>Na2 Ta2 O6>NaTaO3,복합상중Na2 Ta2 O6화NaTaO3지간형성료이질결,능구유효적억제광생전자공혈대적복합。
Pyrochlore structure (Na2 Ta2 O6 ) ,perovskite structure (NaTaO3 ) and composite of sodium tantalate (Na2 Ta2 O6/NaTaO3 ) photocatalysts were controllably synthesized using sodium hexatantalate (Na8 Ta6 O19 ) as precursor via hydrothermal method .The physical properties of the as‐prepared samples were characterized by X‐ray diffraction(XRD) ,field e‐mission scanning electron microscope (FE‐SEM ) and UV‐vis diffuse reflectance spectra (DRS) and the effects of the alkali concentration ,solvent type and pH on the crystal struc‐ture and morphology of the sodium tantalate were discussed .The photocatalytic degradation results of methylene blue indicated that the activity was in the following order :Na2 Ta2 O6/NaTaO3 > Na2 Ta2 O6 > NaTaO3 .The highest photocatalytic activity of Na2 Ta2 O6/NaTaO3 can be attributed to that heterojunction was formed between the Na2 Ta2 O6 and NaTaO3 par‐ticles and the heterojunction significantly prevented the recombination of the electron‐hole pairs .