摘要
在无和有S源(Na2S或硫脲)存在的条件下, 采用十二胺辅助的醇-水热法制备了多孔单斜晶相结构的BiVO4-δ和不同含量S掺杂的BiVO4-δ光催化剂. 利用多种手段表征了催化材料的物化性质, 评价了它们在可见光照射下催化降解亚甲基蓝或甲醛的反应活性. 结果表明, 所制光催化剂为单斜白钨矿晶相结构, 具有多孔橄榄状形貌, 比表面积为8.4-12.5 m2/g, 带隙能为2.40-2.48 eV.在S掺杂BiVO4 表面同时含有Bi5+, Bi4+, V5+和V4+物种. S掺杂对BiVO4-δ光催化剂的活性影响很大. 在可见光下照射下, BiVO4-δS0.08光催化剂对亚甲基蓝和甲醛降解反应显示出最高的光催化活性, 这与其较高的表面氧物种浓度和较低的带隙能相关.
Porous monoclinic bismuth vanadate(BiVO4) and sulfur‐doped bismuth vanadates(BiVO4-δS0.05,BiVO4-δS0.08,and BiVO4-δS0.12) were synthesized by a dodecylamine‐assisted alcohol‐hydrothermal route in the absence and presence of thiourea or Na2S.The physicochemical properties of the materials were characterized and their photocatalytic performance for the degradation of methylene blue and formaldehyde under visible light was evaluated.The samples have a single phase monoclinic scheetlite crystal structure with a porous olive‐like morphology,surface areas of 8.4-12.5m2/g,and bandgap energies of 2.40-2.48 eV.Surface Bi5+,Bi3+,V5+,and V4+ species were present on the S‐doped BiVO4-δ samples.Sulfur doping influenced the surface Bi5+/Bi3+,V5+/V4+,and Oads/O latt molar ratios,and the amount of sulfur doped had an important effect on the photocatalytic performance.Under visible light,BiVO4-δS0.08 performed the best in the photodegradation of methylene blue and formaldehyde.A higher surface oxygen species concentration and a lower bandgap energy were responsible for the excellent visible light photocatalytic performance of BiVO4-δS0.08.
出处
《催化学报》
SCIE
EI
CAS
CSCD
北大核心
2013年第8期1617-1626,共10页
基金
supported by the National Natural Science Foundation of China (21077007)
the Discipline and Postgraduate Education Foundation (005000541212014)
the Funding Project for Academic Human Resources Development in Institutions of Higher Learning under the Jurisdiction of Beijing Municipality (PHR201107104)
Hong Kong Baptist University Foundation (FRG2/09‐10/023)~~
关键词
硫掺杂
钒酸铋
可见光催化
橄榄状形貌
亚甲基蓝降解
甲醛水溶液降解
Sulfur doping Bismuth vanadate Visible‐light‐driven photocatalyst Olive‐like morphology Methlyene blue degradation Formaldehyde degradation