Investigation on the Edge Doping Process of Nitrogen-Doped Carbon Materials by In Situ Pyrolysis Mass Spectrometry and Laser-Induced Acoustic Desorption Mass Spectrometry

Author:

Jiang Yihuang1,Shi Zaifa1,Zeng Qingjie1,Zhang Jiangle1,Deng Zefeng1,Wang Qiaolin23,Yang Jing1,Yu Jingxiong4,Qin Zhengbo2ORCID,Tang Zichao1

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China

2. Anhui Province Key Laboratory of Optoelectric Materials Science and Technology, School of Physics and Electronic Information, Anhui Normal University, Wuhu 241002, China

3. Key Laboratory of High Power Laser and Physics, Chinese Academy of Sciences, Shanghai 201800, China

4. Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China

Abstract

Nitrogen-doped carbon materials demonstrate high performance as electrodes in fuel cells and higher oxygen reduction reactivity than traditional Pt-based electrodes. However, the formation process of nitrogen-doped carbon materials has long been a mystery. In this study, the formation mechanism of nitrogen-doped carbon materials from polyaniline (PANI) pyrolysis was studied by the combination of in situ pyrolysis vacuum ultraviolet photoionization time-of-flight mass spectrometry (Py-VUVPI-TOF MS) and substrate-enhanced, laser-induced acoustic desorption source time-of-flight mass spectrometry (SE-LIAD-TOF MS). The initial pyrolysis species, including free radicals and intermediates, were investigated via in situ Py-VUVPI-TOF MS during the temperature-programmed desorption process (within tens of microseconds). The pyrolysis residues were collected and further investigated via SE-LIAD-TOF MS, revealing the product information of the initial pyrolysis products. The results show that the edge doping of carbon materials depends on free radical reactions rather than the direct substitution of carbon atoms by nitrogen atoms. Meanwhile, pyrrole nitrogen and pyridine nitrogen are formed by the free radical cyclization reaction and the amino aromatization reaction at the initial stage of pyrolysis, while the formation of graphitic nitrogen depends on the further polymerization reaction of pyrrole nitrogen and pyridine nitrogen.

Funder

National Key Research and Development Program of China

National Science Foundation of China

National Natural Science Foundation of China Youth Science Fund

University Cooperation and Innovation Program of Anhui

Open Foundation of Key Laboratory of High Power Laser and Physics, Chinese Academy of Sciences

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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