Synthesis of unused-wood-derived C-Fe-N catalysts for oxygen reduction reaction by heteroatom doping during hydrothermal carbonization and subsequent carbonization in nitrogen atmosphere

Author(s):  
Yasuto Goto ◽  
Yuta Nakayasu ◽  
Hiroya Abe ◽  
Yuto Katsuyama ◽  
Takashi Itoh ◽  
...  

There is an urgent need to develop renewable sources of energy and use existing resources in an efficient manner. In this study, in order to improve the utilization of unused biomass and develop green processes and sustainable technologies for energy production and storage, unused Douglas fir sawdust (SD) was transformed into catalysts for the oxygen reduction reaction. Fe and N were doped into SD during hydrothermal carbonization, and the N- and Fe-doped wood-derived carbon (Fe/N/SD) was carbonized in a nitrogen atmosphere. After the catalyst had been calcined at 800°C, its showed the highest current density (−5.86 mAcm −2 at 0.5 V versus reversible hydrogen electrode or RHE) and E onset value (0.913 V versus RHE). Furthermore, its current density was higher than that of Pt/C (20 wt% Pt) (−5.66 mA cm −2 @0.5 V versus RHE). Finally, after 50 000 s, the current density of sample Fe/N/SD (2 : 10 : 10) remained at 79.3% of the initial value. Thus, the synthesized catalysts, which can be produced readily at a low cost, are suitable for use in various types of energy generation and storage devices, such as fuel cells and air batteries. This article is part of the theme issue ‘Bio-derived and bioinspired sustainable advanced materials for emerging technologies (part 2)’.

2016 ◽  
Vol 18 (38) ◽  
pp. 26572-26578 ◽  
Author(s):  
He Feng ◽  
Lei Wang ◽  
Lu Zhao ◽  
Chungui Tian ◽  
Peng Yu ◽  
...  

The exploration of low-cost and highly efficient non-platinum electrocatalysts for the oxygen reduction reaction (ORR) is vital for renewable systems.


Author(s):  
M. Daarain Haider ◽  
Naseem Iqbal ◽  
Syed Aun M. Rizvi ◽  
Tayyaba Noor ◽  
Saadia Hanif ◽  
...  

Abstract In the present study, the catalytic activity of copper-loaded cobalt-based metal–organic framework (ZIF-67) composites was studied for their electrochemical oxygen reduction reaction (ORR). The Cu-ZIF-67 composite was prepared by the solvothermal method. After pyrolysis under argon atmosphere at 700 °C, the composite was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FTIR). The electrochemical activity of the composites was tested for ORR in 0.1 M alkaline media using the three-electrode system by cyclic voltammetry (CV), Tafel plots, and electrochemical impedance spectroscopy (EIS). The composites showed variable activity with a current density of 1.32 mA cm−2 at 0.71 V (versus reversible hydrogen electrode (RHE)) onset potential for 70 wt% Cu-ZIF-67, 7.5 mA cm−2 at 0.82 V (versus RHE) onset potential for 50 wt% Cu-ZIF-67, and 11.85 mA cm−2 at 0.85 V (versus RHE) for 30% Cu-ZIF-67. The increasing ratio of the ZIF-67 effect can be attributed to the increased activity of ZIF-67 with the synergistic effect of Cu toward increased current density.


2021 ◽  
pp. 2102974
Author(s):  
Jingyu Feng ◽  
Rongsheng Cai ◽  
Emanuele Magliocca ◽  
Hui Luo ◽  
Luke Higgins ◽  
...  

2020 ◽  
Vol 9 (1) ◽  
pp. 843-852
Author(s):  
Hunan Jiang ◽  
Jinyang Li ◽  
Mengni Liang ◽  
Hanpeng Deng ◽  
Zuowan Zhou

AbstractAlthough Fe–N/C catalysts have received increasing attention in recent years for oxygen reduction reaction (ORR), it is still challenging to precisely control the active sites during the preparation. Herein, we report FexN@RGO catalysts with the size of 2–6 nm derived from the pyrolysis of graphene oxide and 1,1′-diacetylferrocene as C and Fe precursors under the NH3/Ar atmosphere as N source. The 1,1′-diacetylferrocene transforms to Fe3O4 at 600°C and transforms to Fe3N and Fe2N at 700°C and 800°C, respectively. The as-prepared FexN@RGO catalysts exhibited superior electrocatalytic activities in acidic and alkaline media compared with the commercial 10% Pt/C, in terms of electrochemical surface area, onset potential, half-wave potential, number of electrons transferred, kinetic current density, and exchange current density. In addition, the stability of FGN-8 also outperformed commercial 10% Pt/C after 10000 cycles, which demonstrates the as-prepared FexN@RGO as durable and active ORR catalysts in acidic media.


2018 ◽  
Vol 42 (3) ◽  
pp. 2081-2088 ◽  
Author(s):  
Man Zhang ◽  
Wei Hong ◽  
Ruinan Xue ◽  
Lingzhi Li ◽  
Guanbo Huang ◽  
...  

At present, low-cost and efficient electrocatalysts for accelerating the oxygen reduction reaction in fuel cells are highly desired.


RSC Advances ◽  
2017 ◽  
Vol 7 (89) ◽  
pp. 56375-56381 ◽  
Author(s):  
Xinxin Jin ◽  
Yu Jiang ◽  
Qi Hu ◽  
Shaohua Zhang ◽  
Qike Jiang ◽  
...  

Low-cost dual transition metal (Fe and Co) based non-noble metal electrocatalysts (NNMEs) with large surface area and porous structure boost oxygen reduction reaction (ORR) performance in alkaline solution.


2021 ◽  
Author(s):  
Fengjiao Yu ◽  
Qi Ying ◽  
Shaofeng Ni ◽  
Chenxue Li ◽  
Daxiang Xue ◽  
...  

Large-scale application of rechargeable Zn-air batteries requires low-cost electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as alternatives to noble metals. Herein, FeCo nanoparticles embedded in N-doped...


2020 ◽  
Vol 45 (11) ◽  
pp. 6994-7004 ◽  
Author(s):  
Chengdong Wang ◽  
Songlin Zhang ◽  
Mingxun Zheng ◽  
Ruoyu Shu ◽  
Shengxu Gu ◽  
...  

Nanomaterials ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 742 ◽  
Author(s):  
Seonghee Kim ◽  
Shuhei Kato ◽  
Takahiro Ishizaki ◽  
Oi Lun Li ◽  
Jun Kang

Metal-air batteries are attracting increasing attention as a superior renewable energy conversion device due to their high performance and strong potential. However, the high cost and low stability of the current Pt catalyst is the main obstacle preventing wide industrial application. In this work, we applied a plasma process to fabricate aniline and a transition metals electrode (Fe, Co, Ni) as the carbon-nitrogen and the metal nanoparticle (NP) precursors, respectively, for selective metal/amino-N-doped carbon catalysts. All three as-synthesized catalysts exhibited dominant amino-N as the major C–N bonding state. In electrochemical testing, Co/amino-N-doped carbon showed positive E1/2 potential (0.83 V vs. Reversible Hydrogen Electrode (RHE)). In addition, the calculated electron transfer number (n) of Co/amino-N-doped carbon at 0.5 V vs. RHE was 3.81, which was only slightly less than that of commercial Pt/C (3.97). This superior performance of transition metal/amino-N-doped carbon promotes it as an economical oxygen reduction reaction (ORR) electrocatalyst to replace expensive Pt/C in metal-air batteries.


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