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用于聚合物电解质膜燃料电池的高性能无铂氧还原反应和氢氧化反应催化剂。

High-performance Platinum-free oxygen reduction reaction and hydrogen oxidation reaction catalyst in polymer electrolyte membrane fuel cell.

作者信息

Chandran Priji, Ghosh Arpita, Ramaprabhu Sundara

机构信息

Alternative Energy and Nanotechnology Laboratory (AENL), Nano-Functional Materials and Technology Centre (NFMTC), Department of Physics, Indian Institute of Technology Madras, Chennai, Tamil Nadu, 600036, India.

出版信息

Sci Rep. 2018 Feb 26;8(1):3591. doi: 10.1038/s41598-018-22001-9.

DOI:10.1038/s41598-018-22001-9
PMID:29483545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5827662/
Abstract

The integration of polymer electrolyte membrane fuel cell (PEMFC) stack into vehicles necessitates the replacement of high-priced platinum (Pt)-based electrocatalyst, which contributes to about 45% of the cost of the stack. The implementation of high-performance and durable Pt metal-free catalyst for both oxygen reduction reaction (ORR) and hydrogen oxidation reaction (HOR) could significantly enable large-scale commercialization of fuel cell-powered vehicles. Towards this goal, a simple, scalable, single-step synthesis method was adopted to develop palladium-cobalt alloy supported on nitrogen-doped reduced graphene oxide (PdCo/NG) nanocomposite. Rotating ring-disk electrode (RRDE) studies for the electrochemical activity towards ORR indicates that ORR proceeds via nearly four-electron mechanism. Besides, the mass activity of PdCo/NG shows an enhancement of 1.6 times compared to that of Pd/NG. The full fuel cell measurements were carried out using PdCo/NG at the anode, cathode in conjunction with Pt/C and simultaneously at both anode and cathode. A maximum power density of 68 mW/cm is accomplished from the simultaneous use of PdCo/NG as both anode and cathode electrocatalyst with individual loading of 0.5 mg/cm at 60 °C without any backpressure. To the best of our knowledge, the present study is the first of its kind of a fully non-Pt based PEM full cell.

摘要

将聚合物电解质膜燃料电池(PEMFC)电堆集成到车辆中需要替换高价的铂(Pt)基电催化剂,该催化剂约占电堆成本的45%。开发用于氧还原反应(ORR)和氢氧化反应(HOR)的高性能且耐用的无Pt金属催化剂能够显著推动燃料电池驱动车辆的大规模商业化。为实现这一目标,采用了一种简单、可扩展的单步合成方法来制备负载在氮掺杂还原氧化石墨烯(PdCo/NG)纳米复合材料上的钯钴合金。旋转环盘电极(RRDE)对ORR的电化学活性研究表明,ORR通过近四电子机制进行。此外,PdCo/NG的质量活性比Pd/NG提高了1.6倍。全燃料电池测量是在阳极和阴极使用PdCo/NG结合Pt/C进行的,同时在阳极和阴极都使用PdCo/NG。在60°C且无任何背压的情况下,同时使用PdCo/NG作为阳极和阴极电催化剂,单个负载量为0.5 mg/cm²时,实现了68 mW/cm²的最大功率密度。据我们所知,本研究是首个全非Pt基PEM全电池的此类研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/4eb31d444f63/41598_2018_22001_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/e3b3c9747f60/41598_2018_22001_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/4ad034f7bf45/41598_2018_22001_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/1f5855d108e0/41598_2018_22001_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/5414c65747c6/41598_2018_22001_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/184e43a41295/41598_2018_22001_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/4eb31d444f63/41598_2018_22001_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/e3b3c9747f60/41598_2018_22001_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/4ad034f7bf45/41598_2018_22001_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/1f5855d108e0/41598_2018_22001_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/5414c65747c6/41598_2018_22001_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/184e43a41295/41598_2018_22001_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f30a/5827662/4eb31d444f63/41598_2018_22001_Fig6_HTML.jpg

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