Xu Chenxi, Fan Chanchan, Zhang Xiaole, Chen Haotian, Liu Xiaoteng, Fu Zhaoming, Wang Ranran, Hong Tao, Cheng Jigui
School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009, Anhui, P. R. China.
School of Physics, Henan Normal University, Xinxiang 453007, Henan, P. R. China.
ACS Appl Mater Interfaces. 2020 Apr 29;12(17):19539-19546. doi: 10.1021/acsami.0c02446. Epub 2020 Apr 16.
The metal-support interaction offers electronic, compositional, and geometric effects that could enhance catalytic activity and stability. Herein, a high corrosion resistance and an excellent electrical conductivity MXene (TiCT) hybrid with a carbon nanotube (CNT) composite material is developed as a support for Pt. Such a composite catalyst enhances durability and improved oxygen reduction reaction activity compared to the commercial Pt/C catalyst. The mass activity of Pt/CNT-MXene demonstrates a 3.4-fold improvement over that of Pt/C. The electrochemical surface area of Pt/CNT-TiCT (1:1) catalysts shows only 6% drop with respect to that in Pt/C of 27% after 2000 cycle potential sweeping. Furthermore, the Pt/CNT-TiCT (1:1) is used as a cathode catalyst for single cell and stack, and the maximum power density of the stack reaches 138 W. The structure distortion of the Pt cluster induced by MXene is disadvantageous to the desorption of O atoms. This issue can be solved by adding CNT on MXene to stabilize the Pt cluster. These remarkable catalytic performances could be attributed to the synergistic effect between Pt and CNT-TiCT.
金属-载体相互作用提供了电子、组成和几何效应,这些效应可以提高催化活性和稳定性。在此,开发了一种具有高耐腐蚀性和优异导电性的MXene(TiCT)与碳纳米管(CNT)的复合材料作为Pt的载体。与商业Pt/C催化剂相比,这种复合催化剂提高了耐久性并改善了氧还原反应活性。Pt/CNT-MXene的质量活性比Pt/C提高了3.4倍。经过2000次循环电势扫描后,Pt/CNT-TiCT(1:1)催化剂的电化学表面积相对于Pt/C仅下降了6%,而Pt/C下降了27%。此外,Pt/CNT-TiCT(1:1)被用作单电池和电池堆的阴极催化剂,电池堆的最大功率密度达到138 W。MXene引起的Pt簇结构畸变不利于O原子的解吸。通过在MXene上添加CNT来稳定Pt簇,可以解决这个问题。这些显著的催化性能可归因于Pt与CNT-TiCT之间的协同效应。