scholarly journals Ternary nickel–tungsten–copper alloy rivals platinum for catalyzing alkaline hydrogen oxidation

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Shuai Qin ◽  
Yu Duan ◽  
Xiao-Long Zhang ◽  
Li-Rong Zheng ◽  
Fei-Yue Gao ◽  
...  

AbstractOperating fuel cells in alkaline environments permits the use of platinum-group-metal-free (PGM-free) catalysts and inexpensive bipolar plates, leading to significant cost reduction. Of the PGM-free catalysts explored, however, only a few nickel-based materials are active for catalyzing the hydrogen oxidation reaction (HOR) in alkali; moreover, these catalysts deactivate rapidly at high anode potentials owing to nickel hydroxide formation. Here we describe that a nickel–tungsten–copper (Ni5.2WCu2.2) ternary alloy showing HOR activity rivals Pt/C benchmark in alkaline electrolyte. Importantly, we achieved a high anode potential up to 0.3 V versus reversible hydrogen electrode on this catalyst with good operational stability over 20 h. The catalyst also displays excellent CO-tolerant ability that Pt/C catalyst lacks. Experimental and theoretical studies uncover that nickel, tungsten, and copper play in synergy to create a favorable alloying surface for optimized hydrogen and hydroxyl bindings, as well as for the improved oxidation resistance, which result in the HOR enhancement.

ACS Catalysis ◽  
2021 ◽  
pp. 932-947
Author(s):  
Eliran R. Hamo ◽  
Ramesh K. Singh ◽  
John C. Douglin ◽  
Sian Chen ◽  
Mohamed Ben Hassine ◽  
...  

2013 ◽  
Vol 135 (21) ◽  
pp. 8016-8021 ◽  
Author(s):  
Junya Ohyama ◽  
Takuma Sato ◽  
Yuta Yamamoto ◽  
Shigeo Arai ◽  
Atsushi Satsuma

2021 ◽  
Author(s):  
Weiyan Ni ◽  
Teng Wang ◽  
Florent Heroguel ◽  
Anna Krammer ◽  
seunghwa lee ◽  
...  

The hydroxide exchange membrane fuel cell (HEMFC) is a promising energy conversion technology, but it is limited by the need of platinum-group-metal (PGM) electrocatalysts, especially for the hydrogen oxidation reaction (HOR). Here we report a Ni-based HOR catalyst that exhibits an electrochemical surface area-normalized exchange current density of 70 μA/cm2, the highest among PGM-free catalysts. The catalyst comprises of Ni nanoparticles embedded in a nitrogen-doped carbon support. According to X-ray and ultraviolet photoelectron spectroscopy as well as H2 chemisorption, the electronic interaction between the Ni nanoparticles and its support leads to an optimal hydrogen binding energy, which is the likely origin of its high activity. PGM-free HEMFCs employing this Ni HOR catalyst give a peak power density of 450 mW/cm2, up to 6 times higher than previous best-performing analogous. This work demonstrates the feasibility of efficient PGM-free HEMFCs.<br>


2020 ◽  
Vol 121 ◽  
pp. 106871
Author(s):  
Zhihang Zhou ◽  
Yuanjun Liu ◽  
Junhao Zhang ◽  
Huan Pang ◽  
Guoxing Zhu

2021 ◽  
Author(s):  
Weiyan Ni ◽  
Teng Wang ◽  
Florent Heroguel ◽  
Anna Krammer ◽  
seunghwa lee ◽  
...  

The hydroxide exchange membrane fuel cell (HEMFC) is a promising energy conversion technology, but it is limited by the need of platinum-group-metal (PGM) electrocatalysts, especially for the hydrogen oxidation reaction (HOR). Here we report a Ni-based HOR catalyst that exhibits an electrochemical surface area-normalized exchange current density of 70 μA/cm2, the highest among PGM-free catalysts. The catalyst comprises of Ni nanoparticles embedded in a nitrogen-doped carbon support. According to X-ray and ultraviolet photoelectron spectroscopy as well as H2 chemisorption, the electronic interaction between the Ni nanoparticles and its support leads to an optimal hydrogen binding energy, which is the likely origin of its high activity. PGM-free HEMFCs employing this Ni HOR catalyst give a peak power density of 450 mW/cm2, up to 6 times higher than previous best-performing analogous. This work demonstrates the feasibility of efficient PGM-free HEMFCs.<br>


2017 ◽  
Vol 727 ◽  
pp. 653-656 ◽  
Author(s):  
Run Fu Li ◽  
Hua Li ◽  
Hui Ying Chen ◽  
Jian Xin Xia ◽  
Chun Lin Long

Monodisperse nickel phosphide (Ni5P4) nanoparticles supported on carbon (Ni5P4@C) were in situ synthesized by one step solution-phase route, in which the mixture of trioctyloxide (TOPO) and trioctylphosphine (TOP) was used as solvent, capping agent and phosphor source. Ni5P4nanocrystals were in situ coupled by active carbon simply adding the carbon to the reaction solution. The as-prepared Pt-free Ni5P4 nanocrystals exhibit the enhanced electrocatalytic activity toward hydrogen oxidation reaction (HOR) compared to pure commercial Ni nanoparticles. Therefore, the obtained Ni5P4@C nanocatalyst appears to be promising non precious metal electrocatalysts for HOR.


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