催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2015年
3期
432-438
,共7页
李菊霞%戴卫理%闫俊青%武光军%李兰冬%关乃佳#
李菊霞%戴衛理%閆俊青%武光軍%李蘭鼕%關迺佳#
리국하%대위리%염준청%무광군%리란동%관내가#
五氧化二钽%纳米结构%晶体生长%光催化性质%各向异性生长
五氧化二鐽%納米結構%晶體生長%光催化性質%各嚮異性生長
오양화이단%납미결구%정체생장%광최화성질%각향이성생장
Tantalum pentoxide%Nanostructure%Crystal growth%Photocatalytic property%Anisotropic growth
以聚乙烯醇(PEG)为结构导向剂,利用水热法合成了形貌可控的Ta2O5纳米柱.采用X射线衍射、扫描电镜、透射电镜、漫反射紫外-可见光谱和光致发光光谱对所制备样品进行了表征.考察了结晶时间和Ta2O5/Sr(OH)2摩尔比等合成参数对样品形貌的影响,并在此基础上对Ta2O5纳米粒可能的生长机理进行了推测.结果表明,在PEG和Sr(OH)2存在条件下可以合成形貌可控的Ta2O5纳米柱.研究了紫外光下Ta2O5纳米柱降解罗丹明B的光催化性能,发现Ta2O5的形貌对光催化性能有很大影响, Ta2O5纳米柱的光催化性能与其长度和直径比成线性关系.催化降解反应的表观速率常数最高可达0.156 min–1,且经多次循环使用后,样品仍然保持较高的催化性能.
以聚乙烯醇(PEG)為結構導嚮劑,利用水熱法閤成瞭形貌可控的Ta2O5納米柱.採用X射線衍射、掃描電鏡、透射電鏡、漫反射紫外-可見光譜和光緻髮光光譜對所製備樣品進行瞭錶徵.攷察瞭結晶時間和Ta2O5/Sr(OH)2摩爾比等閤成參數對樣品形貌的影響,併在此基礎上對Ta2O5納米粒可能的生長機理進行瞭推測.結果錶明,在PEG和Sr(OH)2存在條件下可以閤成形貌可控的Ta2O5納米柱.研究瞭紫外光下Ta2O5納米柱降解囉丹明B的光催化性能,髮現Ta2O5的形貌對光催化性能有很大影響, Ta2O5納米柱的光催化性能與其長度和直徑比成線性關繫.催化降解反應的錶觀速率常數最高可達0.156 min–1,且經多次循環使用後,樣品仍然保持較高的催化性能.
이취을희순(PEG)위결구도향제,이용수열법합성료형모가공적Ta2O5납미주.채용X사선연사、소묘전경、투사전경、만반사자외-가견광보화광치발광광보대소제비양품진행료표정.고찰료결정시간화Ta2O5/Sr(OH)2마이비등합성삼수대양품형모적영향,병재차기출상대Ta2O5납미립가능적생장궤리진행료추측.결과표명,재PEG화Sr(OH)2존재조건하가이합성형모가공적Ta2O5납미주.연구료자외광하Ta2O5납미주강해라단명B적광최화성능,발현Ta2O5적형모대광최화성능유흔대영향, Ta2O5납미주적광최화성능여기장도화직경비성선성관계.최화강해반응적표관속솔상수최고가체0.156 min–1,차경다차순배사용후,양품잉연보지교고적최화성능.
Tantalum pentoxide (Ta2O5) nanorods were hydrothermally synthesized using polyethylene glycol (PEG) as a guiding agent. The nanorods were characterized by X‐ray diffraction, scanning and transmission electron microscopies, and diffuse reflectance ultraviolet‐visible and photolumines‐cence spectroscopies. The effects of crystallization duration and Ta2O5/Sr(OH)2 ratio on the product morphology were investigated, and a growth mechanism was proposed. Phase‐pure Ta2O5 nano‐rods with controlled morphology were formed in the presence of PEG and Sr(OH)2, which was nec‐essary to form the nanorods. Sr(OH)2 induced the surface dissolution and re‐growth of Ta2O5. PEG induced the anisotropic growth of Ta2O5 by acting as a capping agent. The products were used to photocatalytically degrade rhodamine B under ultraviolet irradiation. The catalytic activity directly correlated with the length‐diameter ratio of the Ta2O5 nanorods. A maximum apparent reaction rate constant of 0.156 min–1 was obtained. The Ta2O5 nanorods were stable during photocatalytic reac‐tion and could be recycled several times without loss of activity.