Xia Yuzhen, Lei Hangwei, Sun Chuanfu, Wen Xiaohao, Wang Zichen, Hu Guilin, Fang Baizeng
School of Mechanical and Energy Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, China.
Department of Chemical and Biological Engineering, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
Micromachines (Basel). 2022 Oct 26;13(11):1825. doi: 10.3390/mi13111825.
Chemical functionalization of carbon support for Pt catalysts is a promising way to enhance the performance of catalysts. In this study, Pt/C catalysts grafted with various amounts of phenylsulfonic acid groups were prepared under mild conditions. The influence of sulfonic acid groups on the physiochemical characteristics and electrochemical activities of the modified catalysts were studied using X-ray diffraction, X-ray photoelectron spectroscopy, a transmission electron microscope, and cyclic voltammetry (CV). The presence of the chemical groups enhanced the hydrogen adsorption onto/desorption off the Pt surface during the CV cycling. In contrast, the hydrogen peaks of the grafted catalysts increased after 500 CV cycles, especially for Pt (111) facets. The highest electrochemical surface area (ECSA) after the aging test was obtained for the catalyst with 18.0 wt.% graft, which was ca. 87.3% higher than that of the non-functionalized Pt catalyst. In the density functional theory (DFT) calculation, it was proven that SO3H adsorption on the crystalline was beneficial for Pt stability. The adsorption energy and bond distance of the adsorbed SO3H on Pt (110), (100), and (111) surfaces were calculated. All the stable configurations were obtained when O from S-O single bond or S was bound to the Pt surface, with the adsorption energy following the trend of (111)F > (100)H > (110)H. This result was consistent with the ECSA experiment, which explained the high electrochemical stability of the sulfonic acid groups-grafted Pt/C catalyst.
对用于铂催化剂的碳载体进行化学功能化是提高催化剂性能的一种很有前景的方法。在本研究中,在温和条件下制备了接枝有不同量苯磺酸基团的Pt/C催化剂。使用X射线衍射、X射线光电子能谱、透射电子显微镜和循环伏安法(CV)研究了磺酸基团对改性催化剂的物理化学特性和电化学活性的影响。在CV循环过程中,化学基团的存在增强了氢在铂表面的吸附/脱附。相比之下,接枝催化剂的氢峰在500次CV循环后增加,特别是对于Pt(111)晶面。老化试验后,接枝量为18.0 wt.%的催化剂获得了最高的电化学表面积(ECSA),比未功能化的铂催化剂高约87.3%。在密度泛函理论(DFT)计算中,证明了SO3H在晶体上的吸附有利于铂的稳定性。计算了吸附在Pt(110)、(100)和(111)表面的SO3H的吸附能和键距。当S-O单键中的O或S与铂表面结合时,均获得了所有稳定构型,吸附能遵循(111)F > (100)H > (110)H的趋势。该结果与ECSA实验一致,解释了磺酸基团接枝的Pt/C催化剂的高电化学稳定性。