Department of Energy Systems Engineering, Yasar University , 35100 Izmir, Turkey.
Laboratory for Physical Chemistry of Surfaces, Eindhoven University of Technology , 5600 MB Eindhoven, The Netherlands.
Langmuir. 2017 Oct 31;33(43):11919-11929. doi: 10.1021/acs.langmuir.7b02215. Epub 2017 Oct 19.
The adsorption and decomposition of acetaldehyde and acetic acid were studied on Rh(100) to gain insight into the interaction of aldehyde and carboxyl groups of biomass-derived molecules with the surface. Temperature-programmed reaction spectroscopy (TPRS) was used to monitor gaseous reaction products, whereas Reflection absorption infrared spectroscopy (RAIRS) was used to determine the nature of surface intermediates and reaction paths. The role of adsorbate interactions in oxygenate decomposition chemistry was also investigated by varying the surface coverage. Acetaldehyde adsorbs in an η(C, O) configuration for all coverages, where the carbonyl group binds to the surface via the C and O atoms. Decomposition occurs below room temperature (180-280 K) via C-H and C-C bond breaking, which releases CO, H, and CH species on the surface. At low coverage, CH dehydrogenation dominates and surface carbon is produced alongside H and CO. At high coverage, about 60% of the CH hydrogenates to form methane, whereas only 40% of the CH decomposes further to surface carbon. Acetic acid adsorbs dissociatively on the Rh(100) surface via O-H bond scission, forming a mixture of mono- and bidentate acetate. The decomposition of acetate proceeds via two different pathways: (i) deoxygenation via C-O and C-C bond scissions and (ii) decarboxylation via C-C bond scission. At low coverage, the decarboxylation pathway dominates, a process that occurs at slightly above room temperature (280-360 K) and produces CO and CH, where the latter decomposes further to surface carbon and H. At high coverage, both decarboxylation and deoxygenation occur, slightly, above room temperature (280-360 K). The resulting O adatoms produced in the deoxygenation path react with surface hydrogen or CO to form water and CO, respectively. The CH species dehydrogenate to surface carbon for all coverages. Our findings suggest that oxygenates with a C═O functionality and an alkyl end react on the Rh(100) surface to produce synthesis gas and small hydrocarbons whereas CO and synthesis gas are produced when oxygenates with a COOH functionality and an alkyl end react with the Rh(100) surface. For both cases, carbon accumulation occurs on the surface.
研究了 Rh(100) 上的乙醛和乙酸的吸附和分解,以深入了解生物质衍生分子的醛基和羧基与表面的相互作用。程序升温反应光谱(TPRS)用于监测气态反应产物,而反射吸收红外光谱(RAIRS)用于确定表面中间体和反应途径的性质。通过改变表面覆盖率,还研究了吸附物相互作用在含氧物分解化学中的作用。乙醛在所有覆盖度下都以η(C,O)构型吸附,其中羰基通过 C 和 O 原子与表面结合。在室温以下(180-280 K)通过 C-H 和 C-C 键断裂分解,在表面上释放 CO、H 和 CH 物种。在低覆盖度下,CH 脱氢占主导地位,同时生成表面碳、H 和 CO。在高覆盖度下,约 60%的 CH 加氢形成甲烷,而只有 40%的 CH 进一步分解形成表面碳。乙酸通过 O-H 键断裂在 Rh(100)表面上离解吸附,形成单和双齿乙酸的混合物。乙酸盐的分解通过两条不同的途径进行:(i) 通过 C-O 和 C-C 键断裂脱氧,(ii) 通过 C-C 键断裂脱羧。在低覆盖度下,脱羧途径占主导地位,该过程在略高于室温(280-360 K)下发生,产生 CO 和 CH,后者进一步分解形成表面碳和 H。在高覆盖度下,脱羧和脱氧都发生在略高于室温(280-360 K)的温度下。脱氧途径中生成的 O adatoms 与表面氢或 CO 反应分别形成水和 CO。所有覆盖度下的 CH 物种脱氢形成表面碳。我们的研究结果表明,具有 C═O 官能团和烷基末端的含氧物在 Rh(100)表面上反应生成合成气和小烃类,而具有 COOH 官能团和烷基末端的含氧物与 Rh(100)表面反应生成 CO 和合成气。在这两种情况下,碳都会在表面上积累。