Aqueous phase reforming of methanol (APRM) is simple, inexpensive and provides a high hydrogen gravimetric density of 18.8 wt%, and so is superior to traditional gas-phase reactions performed at relatively… Click to show full abstract
Aqueous phase reforming of methanol (APRM) is simple, inexpensive and provides a high hydrogen gravimetric density of 18.8 wt%, and so is superior to traditional gas-phase reactions performed at relatively high temperatures. In the present work, the interface between Pt nanoparticles and a TiN support was modified using a highly dispersed amorphous LaO x phase. The resulting Pt/LaO x /TiO(N) exhibited enhanced activity and long-term stability during the APRM reaction under base-free conditions compared with Pt catalysts supported on unmodified TiN or crystalline La2O3. The interfacial amorphous LaO x phase promoted the deposition of small Pt nanoparticles having a narrow size distribution, and also generated electron-deficient Pt. An assessment of kinetic isotope data and theoretical investigations demonstrated that the cationic Pt nanoparticles facilitated the cleavage of O-H and C-H bonds in methanol while the amorphous LaO x enhanced the dissociation of water, thus enabling the water-gas shift reaction under mild conditions.
               
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