Controlling phase transfer of molybdenum carbides by various metals for highly efficient hydrogen production

The a phase Mo carbide has been widely investigated recently for its high activity in hydrogen production from water gas shift (WGS) reaction. However, high loading of noble metals as well as high economic and environmental cost derived from high-temperature ammonification and carbonization process will lead to high cost of hydrogen production. Thus, the efficient controlling of phase transfer is promising. Herein, metals (Au, Pt, Rh, Cu) with a wide range of loadings were impregnated on flame spray pyrolysis (FSP) made MoO3 to produce Mo carbides by one-step carbonization. A breakthrough high metal-normalized hydrogen production rate of 213 mmol H-2.g(metal)(-1).s(-1) was achieved on 0.025 wt% Rh/MoCx, which was much higher than Pt and Au based Mo carbides ever reported. The addition of trace Rh induced direct MoO3 transformation to high purity alpha-MoC1-x in one-step carbonization instead of two-steps ammonification and carbonization process. In comparison to Rh, the addition of Pt, Au and Cu tend to transfer MoO3 into beta-Mo2C at the same conditions. Besides, the one with 2 wt% Rh exhibited high stability in WGS reaction even at high temperature (300 degrees C) due to its inhibition on carbides oxidation induced by H2O. We demonstrate that it is feasible to control phase transfer of Mo carbides even by trace amount of metals to simplify the production process of catalysts. The catalytic performance improved by Rh in aspects of both activity and stability provides a guide for producing more stable Mo carbides catalysts. (C) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

Automated summary

Recently, α-phase Mo carbide has attracted attention for its high activity in the water gas shift reaction. By impregnating metals (Au, Pt, Rh, Cu) on MoO3 made by flame spray pyrolysis, Mo carbides were successfully produced in one-step carbonization process. The addition of trace Rh led to direct transformation of MoO3 to α-MoC1-x and exhibited high stability in the WGS reaction even at high temperatures.