Abstract
SBA-15-loaded RuCo alloy nanoparticle catalysts (Ru(x)Co(y)/S15-SU) for the efficient catalysis of hydrogen storage by various liquid organic hydrogen carriers (LOHCs) were prepared via strong electrostatic adsorption (SEA)-ultrasonic in-situ reduction (UR) technology. The above prepared catalysts were subjected to a series of characterization, such as XPS, H(2)-TPD/TPR, N(2) adsorption-desorption, ICP, CO-chemisorption, FT-IR, XRD and TEM. Ru(3+) and Co(2+) were evenly anchored on the surface of SBA-15 by SEA, and ultrafine RuCo alloy nanoparticles were formed by UR without any chemical reducing or stabilizing agents. The addition of Co enhanced the dispersion and antioxidant capacity of the RuCo alloy NPs with an average particle size of 2.07 nm and increased the number of catalytically active sites. The synergistic effect of ultrafine particle size and electron transfer between Co and Ru improved the catalytic performance of monobenzyltoluene (MBT) for hydrogen storage. SEA-UR technology strengthened the coordination effect between RuCo alloy NPs and Si-OH, which enhanced the catalytic stability. H(2)-TPD and H(2)-TPR indicated that the addition of Co led to more activated H(2) to produce hydrogen overflow. For the hydrogenation of MBT, the produced Ru(2)Co(1)/S15-SU showed excellent catalytic performance. The hydrogen storage efficiency of MBT was 99.98 % under 110 °C and 6 MPa H(2) for 26 min, and the TOF was 145 min(-1), which is significantly superior to that of Ru/S15-SU catalyst and that reported in the literature. The hydrogen storage efficiency was still as high as 99.7 % after ten cycles, which was much better than that of Ru/S15-SU and commercial 5 wt% Ru/Al(2)O(3). Ru(2)Co(1)/S15-SU is also suitable for efficiently catalyzing hydrogen storage of N-ethylcarbazole, dibenzyltoluene and acenaphthene.