Li Jinrong,Yu Xianghui,Sun Qi,Peng Yong,Cao Shuang,Hou Chun-Chao,Xu Qiang
PtCo nanoalloys (NAs) deposited on carbon black are emerging as robust electrocatalysts for addressing the sluggish kinetic issue of oxygen reduction reaction (ORR). However, developing a simple and low-cost method to synthesize PtCo/C with excellent performance is still a great challenge. In this work, a one-pot method was used to successfully obtain the PtCo NAs on commercial carbon supports of acetylene black and Ketjenblack ECP600JD, respectively. Compared with those grown on Ketjenblack ECP600JD, the PtCo NAs grown on acetylene black exhibited higher electrochemical surface area (ECSA) and mass activity (MA), which may be attributed to the different particle sizes of PtCo NAs, distinct hydrophilicity, electroconductivity and charge distribution between the carbon supports and PtCo NAs. Our study provides valuable insights into the optimal design of carbon-supported ORR electrocatalysts with exceptional activity and durability.
Background Compared to propane dehydrogenation (PDH) technology, propane oxidative dehydrogenation (ODHP) technology represents an effective approach to overcoming thermodynamic limitations. Supported boron oxide catalysts demonstrate promising potential by co-producing high-value ethylene while enhancing olefin selectivity. However, the critical challenge impeding the development of boron-based catalysts lies in the evaporation-induced loss of active components (boron oxide) under calcination process. Methods BO x −M ( M = SnO 2 , SiO 2 , MgO, CaO, MgSO 4 , CaSO 4 ) catalysts with 10 wt% boron trioxide loading were prepared by simple co-impregnation method using different supports. Significant findings Compared with other catalysts, the BO x -SnO 2 , BO x -CaSO 4 , and BO x −MgSO 4 systems featuring covalent oxygen-containing supports demonstrated superior catalytic performance, achieving propane conversions of 50.1 %, 49.4 %, and 48.9 %, respectively. Analysis revealed that the covalently bonded oxygen in the support forms covalent bridges with the active BO 3 species, thereby enhancing the stable interactions between the support and active components. This effectively mitigates the loss of active species during calcination and improves the catalytic activity. These findings provide a feasible pathway for developing high-performance catalytic systems for ODHP.
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