无机化学学报
無機化學學報
무궤화학학보
JOURNAL OF INORGANIC CHEMISTRY
2009年
11期
2026-2030
,共5页
低温吸附%Au-TiO_2复合薄膜%光电化学性质%交流阻抗谱
低溫吸附%Au-TiO_2複閤薄膜%光電化學性質%交流阻抗譜
저온흡부%Au-TiO_2복합박막%광전화학성질%교류조항보
low-temperature adsorption%Au-TiO_2 nanocomposite film%photoelectrochemical properties%electrochemical impendence spectroscopy
在低温条件下将预先合成的Au溶胶吸附到TiO_2薄膜上以制备纳米Au-TiO_2复合薄膜,以超高分辨率场发射扫描电镜(FESEM)、X射线衍射(XRD)及X射线光电子能谱(XPS)表征Au-TiO_2膜,并在UV辐照下测定了Au-TiO_2薄膜电极的光电化学性质.纳米Au呈金属态,平均粒径为(4.3±1.2)nm,负载量高,均匀地沉积于TiO_2薄膜表面.光电化学测试表明,沉积纳米Au后,TiO_2电极的光生电流提高近5倍,光生电压明显向负值增大,说明纳米Au可增强光生载流子的分离效率,促进电荷在电极与溶液界面间的转移.Au-TiO_2电极的电荷传递法拉第阻抗(R_α)是TiO_2电极的一半,说明负载的纳米Au粒抑制了光生电子-空穴的复合,提高了电极中载流子浓度.
在低溫條件下將預先閤成的Au溶膠吸附到TiO_2薄膜上以製備納米Au-TiO_2複閤薄膜,以超高分辨率場髮射掃描電鏡(FESEM)、X射線衍射(XRD)及X射線光電子能譜(XPS)錶徵Au-TiO_2膜,併在UV輻照下測定瞭Au-TiO_2薄膜電極的光電化學性質.納米Au呈金屬態,平均粒徑為(4.3±1.2)nm,負載量高,均勻地沉積于TiO_2薄膜錶麵.光電化學測試錶明,沉積納米Au後,TiO_2電極的光生電流提高近5倍,光生電壓明顯嚮負值增大,說明納米Au可增彊光生載流子的分離效率,促進電荷在電極與溶液界麵間的轉移.Au-TiO_2電極的電荷傳遞法拉第阻抗(R_α)是TiO_2電極的一半,說明負載的納米Au粒抑製瞭光生電子-空穴的複閤,提高瞭電極中載流子濃度.
재저온조건하장예선합성적Au용효흡부도TiO_2박막상이제비납미Au-TiO_2복합박막,이초고분변솔장발사소묘전경(FESEM)、X사선연사(XRD)급X사선광전자능보(XPS)표정Au-TiO_2막,병재UV복조하측정료Au-TiO_2박막전겁적광전화학성질.납미Au정금속태,평균립경위(4.3±1.2)nm,부재량고,균균지침적우TiO_2박막표면.광전화학측시표명,침적납미Au후,TiO_2전겁적광생전류제고근5배,광생전압명현향부치증대,설명납미Au가증강광생재류자적분리효솔,촉진전하재전겁여용액계면간적전이.Au-TiO_2전겁적전하전체법랍제조항(R_α)시TiO_2전겁적일반,설명부재적납미Au립억제료광생전자-공혈적복합,제고료전겁중재류자농도.
Au-TiO_2 nanocomposite films were prepared by adsorbing prefabricated Au colloids on TiO_2 films at low temperature. The Au-TiO_2 films were characterized with ultra-high resolution FESEM, XRD and XPS, and their photoelectrochemical properties were measured under UV illumination. Au nanoparticles with an average diameter of (4.3±1.2) nm were homogeneously dispersed on the TiO_2 films with high loading. The photoelectrochemical measurements showed that the photocurrent of TiO_2/Ti electrode was improved about 5 folds, and the photovoltage significantly increased to more negative values after depositing Au nanoparticles. It indicates that Au nanoparticles have the beneficial role in improving the photoinduced charge separation efficiency and promoting the charge transfer at the interface between the electrode and electrolyte. The electrochemical impendence spectroscopy (EIS) analyses revealed that the resistance of charge transfer(R_α) of Au-TiO_2/Ti electrode was reduced to half of that of TiO_2/Ti, indicating that the carrier density in the Au-TiO_2/Ti electrode is increased by suppressing the recombination of photogenerated hole-electron pairs.