功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2015年
5期
5052-5057
,共6页
林治顺%余林%叶飞%孙明
林治順%餘林%葉飛%孫明
림치순%여림%협비%손명
光电催化%石墨烯%TiO2%复合材料
光電催化%石墨烯%TiO2%複閤材料
광전최화%석묵희%TiO2%복합재료
photoelectrocatalytic%graphene%TiO2%composite
对 Hummers 方法进行改进,制备出氧化石墨烯。采用氧化石墨烯和 Ti(SO4)2作为初始反应物,利用Ti(SO4)2水解,在氧化石墨烯层间成核生长纳米TiO2颗粒,制得TiO2/氧化石墨烯复合材料,再通过水合肼进行还原,制得 TiO2/石墨烯复合材料。通过XRD、FE-SEM、HR-TEM、TGA、UV-Vis、BET 和电化学性能测试等测试手段对复合材料进行表征。以复合材料为工作电极,铂电极为对电极,饱和甘汞电极为参比电极,在可见光照射(λ>420 nm)下,通过光电催化降解含偶氮化学健的酸性红 B,对复合材料的催化性能进行研究。结果表明,复合材料对可见光响应良好;在外加电极电压的条件下,复合材料的催化活性得到进一步增强。
對 Hummers 方法進行改進,製備齣氧化石墨烯。採用氧化石墨烯和 Ti(SO4)2作為初始反應物,利用Ti(SO4)2水解,在氧化石墨烯層間成覈生長納米TiO2顆粒,製得TiO2/氧化石墨烯複閤材料,再通過水閤肼進行還原,製得 TiO2/石墨烯複閤材料。通過XRD、FE-SEM、HR-TEM、TGA、UV-Vis、BET 和電化學性能測試等測試手段對複閤材料進行錶徵。以複閤材料為工作電極,鉑電極為對電極,飽和甘汞電極為參比電極,在可見光照射(λ>420 nm)下,通過光電催化降解含偶氮化學健的痠性紅 B,對複閤材料的催化性能進行研究。結果錶明,複閤材料對可見光響應良好;在外加電極電壓的條件下,複閤材料的催化活性得到進一步增彊。
대 Hummers 방법진행개진,제비출양화석묵희。채용양화석묵희화 Ti(SO4)2작위초시반응물,이용Ti(SO4)2수해,재양화석묵희층간성핵생장납미TiO2과립,제득TiO2/양화석묵희복합재료,재통과수합정진행환원,제득 TiO2/석묵희복합재료。통과XRD、FE-SEM、HR-TEM、TGA、UV-Vis、BET 화전화학성능측시등측시수단대복합재료진행표정。이복합재료위공작전겁,박전겁위대전겁,포화감홍전겁위삼비전겁,재가견광조사(λ>420 nm)하,통과광전최화강해함우담화학건적산성홍 B,대복합재료적최화성능진행연구。결과표명,복합재료대가견광향응량호;재외가전겁전압적조건하,복합재료적최화활성득도진일보증강。
Graphene oxide was prepared by the modified Hummers method.Using the graphene oxide and Ti (SO4 )2 as the initial reactants,TiO2/graphene oxide composite was prepared by nucleation growth of TiO2 nan-oparticles in the graphene oxide interlayer after Ti(SO4 )2 hydrolysis.Then,TiO2/graphene composite was pre-pared through reduction by hydrazine hydrate.The composite was characterized by XRD,FE-SEM,HR-TEM, TGA,UV-Vis,TBE and the electrochemical measurements.Under visible light irradiation(λ>420 nm),using the composite as working electrode,platinum electrode as counter electrode,and saturated calomel electrode as reference electrode,the photoelectrocatalytic activity of the composite for the decomposition of acid red B which contains azo chemical health was studied.The results showed that the composite has a good response to the visi-ble light,and the catalytic activity of the composite was increased under the condition of increased electrode voltage.