Interfacial Functionalization of TiO2 with Smart Polymers: pH-Controlled Switching of Photocurrent Direction

被引:32
作者
Chen, Da [1 ,2 ]
Li, Jinghong [2 ]
机构
[1] China Jiliang Univ, Coll Mat Sci & Engn, Hangzhou 310018, Peoples R China
[2] Tsinghua Univ, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
POLY(ACRYLIC ACID); LIGHT-DRIVEN; SEMICONDUCTOR ELECTRODES; CATHODIC PHOTOCURRENTS; GOLD NANOPARTICLES; IONIC-STRENGTH; ACRYLIC-ACID; THIN-FILMS; SURFACE; TEMPERATURE;
D O I
10.1021/jp100969a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
TiO2/P(NIPAM-AA) nanocomposites were successfully obtained by the incorporation of TiO2 nanoparticles (P25, commercial TiO2 nanoparticles from Degussa) with pH-stimuli responsive smart polymer [poly(N-isopropylacrylamide-co-acrylic acid), P(NIPAM-AA)]. Compared with the pure TiO2 nanoparticles, the incorporation of TiO2 nanoparticles with smart polymer P(NIPAM-AA) produced a significant effect on its photocurrent activities. The photocurrent behavior of TiO2/P(NIPAM) nanocomposites photoelectrode was tunable in response to pH stimuli. It was found that the nanocomposites photoelectrode produced an anodic photocurrent at pH 3.0, whereas it generated a relatively small cathodic photocurrent at pH 10.0. The pH-dependent swelling behavior of smart polymer played an important role in the pH-induced photocurrent switching, which actually was an intrinsic feature resulting from a specific electronic structure of the surface-modified semiconductor with smart polymer. The combination of the photoelectrochemical properties of inorganic semiconductor nanoparticles with external stimuli-responsive properties of organic smart polymers provides a new opportunity for controllable photocurrent switching.
引用
收藏
页码:10478 / 10483
页数:6
相关论文
共 42 条
[1]   A hybrid semiconductor electrode for wavelength-controlled switching of the photocurrent direction [J].
Beranek, Radim ;
Kisch, Horst .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (07) :1320-1322
[2]   Equilibrium and kinetic aspects of the uptake of poly(ethylene oxide) by copolymer microgel particles of N-isopropylacrylamide and acrylic acid [J].
Bradley, M ;
Ramos, J ;
Vincent, B .
LANGMUIR, 2005, 21 (04) :1209-1215
[3]   Microchannel DNA sequencing matrices with a thermally controlled "viscosity switch" [J].
Buchholz, BA ;
Doherty, EAS ;
Albarghouthi, MN ;
Bogdan, FM ;
Zahn, JM ;
Barron, AE .
ANALYTICAL CHEMISTRY, 2001, 73 (02) :157-164
[4]   Preparation and enhanced photoelectrochemical performance of coupled bicomponent ZnO-TiO2 nanocomposites [J].
Chen, Da ;
Zhang, Hao ;
Hu, Song ;
Li, Jinghong .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (01) :117-122
[5]   Surface tailoring for controlled photoelectrochemical properties:: Effect of patterned TiO2 microarrays [J].
Chen, Da ;
Gao, Yanfang ;
Wang, Geng ;
Zhang, Hao ;
Lu, Wu ;
Li, Jinghong .
JOURNAL OF PHYSICAL CHEMISTRY C, 2007, 111 (35) :13163-13169
[6]   Negatively thermoresponsive membranes with functional gates driven by zipper-type hydrogen-bonding interactions [J].
Chu, LY ;
Li, Y ;
Zhu, JH ;
Chen, WM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (14) :2124-2127
[7]   Settling characteristics of composites of PNIPAM microgels and TiO2 nanoparticles [J].
Coutinho, Cecil A. ;
Harrinauth, Reshma K. ;
Gupta, Vinay K. .
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2008, 318 (1-3) :111-121
[8]   Layer-by-layer structured films of TiO2 nanoparticles and poly(acrylic acid) on electrospun nanofibres [J].
Ding, B ;
Kim, J ;
Kimura, E ;
Shiratori, S .
NANOTECHNOLOGY, 2004, 15 (08) :913-917
[9]   Mott-Schottky analysis of nanoporous semiconductor electrodes in dielectric state deposited on SnO2(F) conducting substrates [J].
Fabregat-Santiago, F ;
Garcia-Belmonte, G ;
Bisquert, J ;
Bogdanoff, P ;
Zaban, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (06) :E293-E298
[10]  
Garay MT, 1997, POLYMER, V38, P5091