scholarly journals Enhanced Electrocatalytic Activity and Stability toward the Oxygen Reduction Reaction with Unprotected Pt Nanoclusters

Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 955 ◽  
Author(s):  
Jing Liu ◽  
Jiao Yin ◽  
Bo Feng ◽  
Tao Xu ◽  
Fu Wang

The Pt particles within diameters of 1–3 nm known as Pt nanoclusters (NCs) are widely considered to be satisfactory oxygen reduction reaction (ORR) catalysts due to higher electrocatalytic performance and cost effectiveness. However, the utilization of such smaller Pt NCs is always limited by the synthesis strategies, stability and methanol tolerance of Pt. Herein, unprotected Pt NCs (~2.2 nm) dispersed on carbon nanotubes (CNTs) were prepared via a modified top-down approach using liquid Li as a solvent to break down the bulk Pt. Compared with the commercial Pt/C, the resultant Pt NCs/CNTs catalyst (Pt loading: 10 wt.%) exhibited more desirable ORR catalytic performance in 0.1 M HClO4. The specific activity (SA) and mass activity (MA) at 0.9 V for ORR over Pt NCs/CNTs were 2.5 and 3.2 times higher than those over the commercial Pt/C (Pt loading: 20 wt.%). Meanwhile, the Pt NCs/CNTs catalyst demonstrated more satisfactory stability and methanol tolerance. Compared with the obvious loss (~69%) of commercial Pt/C, only a slight current decrease (~10%) was observed for Pt NCs/CNTs after the chronoamperometric measurement for 2 × 104 s. Hence, the as-prepared Pt NCs/CNTs material displays great potential as a practical ORR catalyst.

2017 ◽  
Vol 19 (31) ◽  
pp. 21003-21011 ◽  
Author(s):  
Zhanwei Xu ◽  
Xiaoli Fan ◽  
Hejun Li ◽  
Hao Fu ◽  
Woon Ming Lau ◽  
...  

Graphene fragments prepared using a wet-grinding method show high catalytic performance for the oxygen reduction reaction.


2019 ◽  
Vol 10 ◽  
pp. 1251-1269
Author(s):  
Stéphane Louisia ◽  
Yohann R J Thomas ◽  
Pierre Lecante ◽  
Marie Heitzmann ◽  
M Rosa Axet ◽  
...  

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) Pt3M (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 H2O2 generated during the oxygen reduction reaction (ORR) have been evaluated in a rotating ring disk electrode experiment. The Pt3M/N-CNT catalysts revealed excellent electrochemical properties compared to a commercial Pt3Co/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 Pt3Co > Pt3Ni, whereas on the annealed N-CNT support, the order was reversed.


2011 ◽  
Vol 306-307 ◽  
pp. 155-158
Author(s):  
Chia Ying Hsieh ◽  
Yi Shiuan Huang ◽  
Jing Shan Do

The mesoporous carbon (MC) synthesized by a one-step method with tetraethyl ortho- silicate (TEOS) as silicon source, sucrose as carbon source and phosphoric acid as active agent, respectively, is used as the support to prepare Pt/MC electrocatalysts. The pore characteristics and the graphitic extend of MC can be adjusted by controlling the carbonation temperature (Tc). The maximum surface area of home-made MC is confirmed and analyzed by BET to be 860.20 m2g-1 with Tc = 900 °C, and the main pore size of MC is 8.70 nm. The maximum mass activity (MA) and specific activity (SA) of the oxygen reduction reaction (ORR) on Pt/MC (P/Si = 0.5, Tc = 900 °C) are experimentally found to be 15.54 A g-1 and 18.05 mA cm-2, respectively.


Materials ◽  
2020 ◽  
Vol 13 (14) ◽  
pp. 3142
Author(s):  
Ruyue Shi ◽  
Ying Huang ◽  
Miaoran Li ◽  
Ying Zhu ◽  
Xuexia He ◽  
...  

Electrocatalysts play an important role in oxygen reduction reaction (ORR) in promoting the reaction process. Although commercial Pt/C exhibits excellent performance in ORR, the low duration, high cost, and poor methanol tolerance seriously restrict its sustainable development and application. TinO2n−1 (3 ≤ n ≤ 10) is a series of titanium sub-oxide materials with excellent electrical conductivity, electrochemical activity, and stability, which have been widely applied in the field of energy storage and catalysis. Herein, we design and synthesize Ti4O7/Ti3O5 (T4/T3) dual-phase nanofibers with excellent ORR catalytic performance through hydrothermal growth, which is followed by a precisely controlled calcination process. The H2Ti3O7 precursor with uniform size can be first obtained by optimizing the hydrothermal growth parameters. By precisely controlling the amount of reducing agent, calcination temperature, and holding time, the T4/T3 dual-phase nanofibers with uniform morphology and coherent interfaces can be obtained. The orientation relationships between T4 and T3 are confirmed to be [ 001 ] T 3 / / [ 031 ] T 4 , ( 100 ) T 3 / / ( 92 6 ¯ ) T 4 , and ( 010 ) T 3 / / ( 1 2 ¯ 6 ) T 4 , respectively, based on comprehensive transmission electron microscopy (TEM) investigations. Furthermore, such dual-phase nanofibers exhibit the onset potential and half-wave potential of 0.90 V and 0.75 V as the ORR electrocatalysts in alkaline media, respectively, which illustrates the excellent ORR catalytic performance. The rotating ring-disk electrode (RRDE) experiment confirmed the electron transfer number of 3.0 for such catalysts, which indicates a mixture of two electron and four electron transfer reaction pathways. Moreover, the methanol tolerance and cycling stability of the catalysts are also investigated accordingly.


2021 ◽  
Vol 23 (7) ◽  
pp. 4454-4454
Author(s):  
Kunran Yang ◽  
Jeremie Zaffran ◽  
Bo Yang

Correction for ‘Fast prediction of oxygen reduction reaction activity on carbon nanotubes with a localized geometric descriptor’ by Kunran Yang et al., Phys. Chem. Chem. Phys., 2020, 22, 890–895, DOI: 10.1039/C9CP04885E.


2019 ◽  
Vol 4 (36) ◽  
pp. 10863-10867
Author(s):  
Yanping Huang ◽  
Weifang Liu ◽  
Shuting Kan ◽  
Penggao Liu ◽  
Hongtao Liu ◽  
...  

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