Louisia Stéphane, Thomas Yohann R J, Lecante Pierre, Heitzmann Marie, Axet M Rosa, Jacques Pierre-André, Serp Philippe
LCC-CNRS, Université de Toulouse, CNRS, INPT, Toulouse, France.
Université Grenoble Alpes, CEA-LITEN/DEHT, 17 rue des martyrs 38000 Grenoble, France.
Beilstein J Nanotechnol. 2019 Jun 21;10:1251-1269. doi: 10.3762/bjnano.10.125. eCollection 2019.
Sulfur- (S-CNT) and nitrogen-doped (N-CNT) carbon nanotubes have been produced by catalytic chemical vapor deposition (c-CVD) and were subject to an annealing treatment. These CNTs were used as supports for small (≈2 nm) PtM (M = Co or Ni) alloyed nanoparticles that have a very homogeneous size distribution (in spite of the high metal loading of ≈40 wt % Pt), using an ionic liquid as a stabilizer. The electrochemical surface area, the activity for the oxygen reduction reaction and the amount of HO generated during the oxygen reduction reaction (ORR) have been evaluated in a rotating ring disk electrode experiment. The PtM/N-CNT catalysts revealed excellent electrochemical properties compared to a commercial PtCo/Vulcan XC-72 catalyst. The nature of the carbon support plays a key role in determining the properties of the metal nanoparticles, on the preparation of the catalytic layer, and on the electrocatalytic performance in the ORR. On N-CNT supports, the specific activity followed the expected order PtCo > PtNi, whereas on the annealed N-CNT support, the order was reversed.
通过催化化学气相沉积(c-CVD)制备了硫掺杂(S-CNT)和氮掺杂(N-CNT)的碳纳米管,并对其进行了退火处理。这些碳纳米管被用作小尺寸(≈2 nm)的PtM(M = Co或Ni)合金纳米颗粒的载体,这些纳米颗粒具有非常均匀的尺寸分布(尽管Pt的金属负载量高达≈40 wt%),使用离子液体作为稳定剂。在旋转环盘电极实验中评估了电化学表面积、氧还原反应活性以及氧还原反应(ORR)过程中产生的HO量。与商业PtCo/Vulcan XC-72催化剂相比,PtM/N-CNT催化剂表现出优异的电化学性能。碳载体的性质在决定金属纳米颗粒的性质、催化层的制备以及ORR中的电催化性能方面起着关键作用。在N-CNT载体上,比活性遵循预期顺序PtCo > PtNi,而在退火的N-CNT载体上,顺序相反。