Amino-terminated diamond surfaces: Photoelectron emission and photocatalytic properties

被引:29
|
作者
Zhu, Di [1 ]
Bandy, Jason A. [1 ]
Li, Shuo [1 ]
Hamers, Robert J. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
Diamond; Photocatalysis; Amine; Amino; Electron emission; Solvated electrons; NEGATIVE-ELECTRON-AFFINITY; DOPED DIAMOND; SOLVATED ELECTRONS; HYDROXYL RADICALS; RATE CONSTANTS; WATER; SEMICONDUCTOR; OXYGEN; METAL; FILM;
D O I
10.1016/j.susc.2016.01.003
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
We report a new approach to making stable negative electron-affinity diamond surfaces by terminating diamond with amino groups (also known as amine groups, -NH2). Previous studies have shown that negative electron affinity can be induced by terminating diamond surfaces with hydrogen, creating a surface dipole favorable toward electron emission. Here, we demonstrate that covalent tethering of positive charges in the form of protonated amino groups, -NH3+, also leads to negative electron affinity (NEA) and facile electron emission into vacuum and into water. Amino-terminated diamond was prepared using a very mild plasma discharge. Valence-band photoemission studies of the amino-terminated diamond samples show a characteristic "NEA" peak, demonstrating that the amino-terminated surface has NEA. Diamond's ability to emit electrons into water was evaluated using photochemical conversion of N-2 to NH3. Time-resolved surface photovoltage studies were used to characterize charge separation at the diamond interface, and Mott-Schottky measurements were performed to characterize band-bending at the diamond-water interface. XPS studies show that the amino-terminated surfaces provide increased chemical resistance to oxidation compared with H-terminated diamond when illuminated with ultraviolet light. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:295 / 301
页数:7
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