scholarly journals Improved Electrocatalytic Activity and Durability of Pt Nanoparticles Supported on Boron-Doped Carbon Black

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 862
Author(s):  
Rui Yao ◽  
Jun Gu ◽  
Haitong He ◽  
Tao Yu

A facile strategy is proposed to synthesize boron-doped ECP600 carbon black (B-ECP600), and the catalyst of Pt supported on boron-doped ECP600 (Pt/B-ECP600) shows smaller particle sizes and a higher electrochemical surface area (95.62 m2·gPt−1) and oxygen reduction reaction activity (0.286 A·mgPt−1 for mass activity; 0.299 mA·cm−2 for area specific activity) compared to the catalyst of Pt supported on ECP600 (Pt/ECP600). The results show that the boron doping of the carbon supports plays an important role in controlling the size and dispersion of Pt nanoparticles and the O2 adsorption/dissociation of the oxygen reduction reaction. A further accelerated durability test proves that boron doping can greatly enhance the stability of carbon support and thus improves the electrochemical performance of the catalyst during the long-time running. All these results suggest boron-doped carbon has great potential for application in fuel cells.

2017 ◽  
Vol 164 (9) ◽  
pp. F995-F1004 ◽  
Author(s):  
Dana Schonvogel ◽  
Julia Hülstede ◽  
Peter Wagner ◽  
Ivar Kruusenberg ◽  
Kaido Tammeveski ◽  
...  

Author(s):  
Sabarinathan Ravichandran ◽  
Narayanamoorthy Bhuvanendran ◽  
Weiqi Zhang ◽  
Qian Xu ◽  
Lindiwe Khotseng ◽  
...  

Abstract Platinum supported on carbon support (Pt/C) is currently the most common and practicable electrocatalyst for the real application of polymer electrolyte membrane fuel cells (PEMFCs). In this work, it was found that the nature of a reducing agent has noteworthy influence on Pt nanoparticles growth and distribution over acid-treated-Vulcan carbon support (Pt/AT-VC), which was employed to catalyze the oxygen reduction reaction (ORR) for PEMFC. Three distinct reducing agents, i.e., sodium borohydride (BH), sodium citrate (CA), and formaldehyde (FMY), were employed for Pt/AT-VC preparation through the impregnation-reduction approach. The impacts of the reducing agent on Pt nanoparticles size and its distribution over carbon support were scrutinized by X-ray diffraction (XRD) and high-resolution transmission electron microscopy (TEM) techniques. The electrocatalytic performance for ORR was subsequently studied by a three-electrode setup with rotating ring-disc electrode (RRDE) characterization and practical fuel cell operation. The ORR kinetics and mechanism were confirmed from RRDE, and it was well correlated with the durability test and single-cell results. Based on the results, the catalysts’ performances for practical PEMFC can be arranged in the order of Pt/AT-VC (BH) < Pt/AT-VC (CA) < Pt/AT-VC (FMY), implying the significance of selecting the reducing agent for the preparation of Pt/C for PEMFC real application.


2021 ◽  
Author(s):  
Kaneyuki Taniguchi ◽  
Jhon Lehman Cuya Huaman ◽  
Dausuke Iwata ◽  
Shun Yokoyama ◽  
Takatoshi Matsumoto ◽  
...  

Alloying Pt with transition elements as electrodes in fuel cells has been proposed to solve the CO poisoning effect besides cost-benefit. Consequently, the use of Ni-Pt nanoparticles (NPs) has been...


2016 ◽  
Vol 55 (24) ◽  
pp. 6842-6847 ◽  
Author(s):  
Tat Thang Vo Doan ◽  
Jingbo Wang ◽  
Kee Chun Poon ◽  
Desmond C. L. Tan ◽  
Bahareh Khezri ◽  
...  

2012 ◽  
Vol 22 (2) ◽  
pp. 390-395 ◽  
Author(s):  
Zhen-Huan Sheng ◽  
Hong-Li Gao ◽  
Wen-Jing Bao ◽  
Feng-Bin Wang ◽  
Xing-Hua Xia

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.


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