Addition of a single chemical functional group to a polymer surface with a mass-separated low-energy ion beam

被引:21
作者
Nowak, P
McIntyre, NS
Hunter, DH
Bello, I
Lau, WM
机构
[1] UNIV WESTERN ONTARIO,DEPT CHEM & SURFACE SCI WESTERN,LONDON,ON N6A 5B7,CANADA
[2] UNIV WESTERN ONTARIO,DEPT MAT ENGN,LONDON,ON N6A 5B9,CANADA
关键词
D O I
10.1002/sia.740231304
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
A mass-separated low-energy ion beam system was used to deliver pure OH+ and NH+ to 15 nm thick polystyrene films on silicon in ultrahigh vacuum. This was done in an effort to produce specific surface chemical functional groups, X-ray photoelectron spectroscopy showed that when the bombardment energy of OH+ exceeded 10 eV, or the dose was higher than 1 x 10(16) ions cm(-2), a mixture of C-OH, C-C=O and C-COOH groups was produced, along with severe damage to the aromatic rings. However, for bombardment at 10 eV with a dose of 1 x 10(16) ions cm(-2), only C-OH (or COR) groups were found, Similarly, bombardment with NH+ at 10 eV and a dose 1 x 10(16) ions cm(-2) induced incorporation of a single nitrogen-containing functionality, The C 1s data indicated that the major chemical functionality on such surfaces in a C-NH2 (or C-NHR) group with a minor component of C-(NH2)(2). Hence, surface functionality can indeed be controlled by altering the molecular nature, energy and dose of the bombarding species.
引用
收藏
页码:873 / 878
页数:6
相关论文
共 24 条
[1]  
Beamson G., 1992, HIGH RESOLUTION XPS, DOI 10.1021/ED070PA25.5
[2]   STUDIES OF REACTIVE ION ETCHING USING COLUTRON HOT-FILAMENT DC PLASMA ION SOURCES [J].
BELLO, I ;
CHANG, WH ;
FENG, XH ;
LAU, WM .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS, 1993, 80-1 :1002-1005
[3]  
BELLO I, 1985, RADIAT EFF, V89, P180
[4]  
BELLO I, 1992, SURF SCI, V271, P468
[5]   POLYMER SURFACE REACTIVITY ENHANCEMENT BY ULTRAVIOLET ARF LASER IRRADIATION - AN X-RAY PHOTOELECTRON-SPECTROSCOPY STUDY OF POLYTETRAFLUOROETHYLENE AND POLYETHYLENETEREPHTHALATE ULTRAVIOLET TREATED SURFACES [J].
CHTAIB, M ;
ROBERFROID, EM ;
NOVIS, Y ;
PIREAUX, JJ ;
CAUDANO, R ;
LUTGEN, P ;
FEYDER, G .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS, 1989, 7 (06) :3233-3237
[6]   THERMAL RECONSTRUCTION OF SURFACE-FUNCTIONALIZED POLY(CHLOROTRIFLUOROETHYLENE) [J].
CROSS, EM ;
MCCARTHY, TJ .
MACROMOLECULES, 1990, 23 (17) :3916-3922
[7]   INTRODUCTION OF CARBOXYLIC-ACID, ALDEHYDE, AND ALCOHOL FUNCTIONAL-GROUPS ONTO THE SURFACE OF POLY(CHLOROTRIFLUOROETHYLENE) [J].
DIAS, AJ ;
MCCARTHY, TJ .
MACROMOLECULES, 1987, 20 (09) :2068-2076
[8]   REMOTE NITROGEN PLASMA TREATMENT OF POLYMERS - POLYETHYLENE, NYLON 6,6, POLY(ETHYLENE VINYL ALCOHOL), AND POLY(ETHYLENE-TEREPHTHALATE) [J].
FOERCH, R ;
HUNTER, DH .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1992, 30 (02) :279-286
[9]   OXIDATION OF POLYETHYLENE SURFACES BY REMOTE PLASMA DISCHARGE - A COMPARISON STUDY WITH ALTERNATIVE OXIDATION METHODS [J].
FOERCH, R ;
MCINTYRE, NS ;
HUNTER, DH .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1990, 28 (01) :193-204
[10]  
FOERCH R, 1991, KUNSTST PLAST MUNICH, V81, P47