Catalyst characterizationBrunauer−Emmet−Teller (BET) surface areas (S BET ) and pore volumes (Vp) of catalysts were measured using a ASIQMO002-2 analyzer (Quantachrome, US) by nitrogen adsorption at liquid nitrogen temperature. The sample (~100 mg) was heated at 200 °C for 6 h to remove the adsorbed gases before test. The chemical composition of catalysts was detected by AXIOSmAX-PETRO XRF (X-ray fluorescence) (PANalytical, Netherlands). The structural parameters and chemical composition of these catalysts are shown in Table S1.Temperature programmed reduction (TPR) studies were carried out in the ChemBET Pulsar-1 automated chemisorption analyzer (Quantachrome, US). The sample was pre-treated by Ar at 120 °C for 120 min. After the sample was cooled to 30 °C, the reduction gas of 5.1 vol% H 2 /Ar was fed into the reactor and temperature was increased linearly to 600 °C at heating rate of 5 °C/min. The consumed gas was monitored by thermal conductivity detector (TCD). The H 2 -TPR profiles of these catalysts are shown in Figure S1. X-ray diffraction (XRD) patterns were obtained with a Rigaku X' pert Pro diffractrometer (PANalytical, Netherlands) with Cu Kα radiation (λ = 0.15418 nm) to investigate the phase composition of fresh catalysts. The measurement conditions was in the 2θ range of 20° -80° with a scanning rate of 0.02 °/step in air at room temperature. The XRD patterns of these catalysts are shown in Figure S2.