Making H2 from light and biomass-derived alcohols: the outstanding activity of newly designed hierarchical MWCNT/Pd@TiO2 hybrid catalysts

被引:39
作者
Beltram, A. [1 ]
Melchionna, M. [1 ]
Montini, T. [1 ,2 ]
Nasi, L. [3 ]
Fornasiero, P. [1 ,2 ]
Prato, M. [1 ,4 ,5 ]
机构
[1] Univ Trieste, INSTM, Dept Chem & Pharmaceut Sci, Via L Giorgieri 1, I-34127 Trieste, Italy
[2] ICCOM CNR Trieste, Via L Giorgieri 1, I-34127 Trieste, Italy
[3] CNR IMEM Inst, Parco Area Sci 37, I-43124 Parma, Italy
[4] CIC biomaGUNE, Nanobiotechnol Lab, Paseo de Miramon 182, San Sebastian 20009, Spain
[5] Ikerbasque, Basque Fdn Sci, Bilbao 48013, Spain
关键词
DOPED TIO2 ELECTRODES; CORE-SHELL CATALYSTS; CARBON NANOTUBES; TITANIUM-DIOXIDE; PHOTOCATALYTIC ACTIVITY; SELECTIVE HYDROGENATION; SOLAR-ENERGY; PD CATALYSTS; LIQUID-PHASE; NANOCOMPOSITES;
D O I
10.1039/c6gc01979j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen evolution is among the most investigated catalytic processes given the importance of H-2 from an industrial and an energy perspective. Achieving H-2 production through green routes, such as water splitting or more realistically photoreforming of alcohols, is particularly desirable. In this work, we achieve a remarkable H-2 productivity through photoreforming of either ethanol or glycerol as a sacrificial electron donor by employing a hybrid nanocatalyst where the properties of multi-walled carbon nanotubes (MWCNTs), Pd nanoparticles and crystalline TiO2 are optimally merged through appropriate engineering of the three components and an optimised synthetic protocol. Catalysts were very active both under UV (highest activity 25 mmol g(-1) h(-1)) and simulated solar light (1.5 mmol h(-1) g(-1)), as well as very stable. Critical to such high performance is the intimate contact of the three phases, each fulfilling a specific task synergistically with the other components.
引用
收藏
页码:2379 / 2389
页数:11
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