Assisted deprotonation of formic acid on Cu(111) and self-assembly of 1D chains

被引:37
作者
Baber, Ashleigh E. [1 ]
Mudiyanselage, Kumudu [1 ]
Senanayake, Sanjaya D. [1 ]
Beatriz-Vidal, Alba [1 ]
Luck, Kyle A. [1 ]
Sykes, E. Charles H. [2 ]
Liu, Ping [3 ]
Rodriguez, Jose A. [1 ]
Stacchiola, Dario J. [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Tufts Univ, Dept Chem, Medford, MA 02155 USA
[3] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
GAS SHIFT REACTION; TEMPERATURE-PROGRAMMED DESORPTION; SCANNING-TUNNELING-MICROSCOPY; METHANOL SYNTHESIS; STRUCTURE SENSITIVITY; THERMAL-DESORPTION; CO2; HYDROGENATION; COPPER SURFACES; ACTIVE-SITE; FORMATE;
D O I
10.1039/c3cp51533h
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
Formic acid (HCOOH) deprotonates on the open surfaces of Cu(110) and Cu(100) when exposed at 300 K. However, this does not occur on the close-packed surface of clean Cu(111). In this study, we show that the deprotonation of formic acid on atomically flat Cu(111) surfaces can be induced by pre-adsorbing polymeric formic acid clusters at low temperatures, and then annealing the system to break the acidic O-H bond of HCOOH adsorbed on the edges of the polymeric clusters. The thermal activation of HCOOH to bidentate formate was studied using a combination of infrared reflection absorption spectroscopy, scanning tunneling microscopy, X-ray photoelectron spectroscopy, and near edge X-ray absorption fine structure spectroscopy. Extended 1D formate structures self-assemble due to a templating effect introduced by the formation of long alpha-polymeric formic acid chains commensurate with the substrate.
引用
收藏
页码:12291 / 12298
页数:8
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