B. Sc. Ángel Chávez-Hernández, Dr. Carlos M. Ramos-Castillo, Prof. Amelia Olivas, Dr. Anabel D. Delgado, Prof. Minerva Guerra-Balcázar, Prof. Lorena Álvarez-Contreras, Dr. Noé Arjona
{"title":"Surface Engineering of N-Doped Carbon Derived from Polyaniline for Primary Zinc-Air Batteries","authors":"B. Sc. Ángel Chávez-Hernández, Dr. Carlos M. Ramos-Castillo, Prof. Amelia Olivas, Dr. Anabel D. Delgado, Prof. Minerva Guerra-Balcázar, Prof. Lorena Álvarez-Contreras, Dr. Noé Arjona","doi":"10.1002/cnma.202400361","DOIUrl":null,"url":null,"abstract":"<p>Zinc-air batteries (ZABs) with metal-free cathodes are considered environmentally friendly and cost-effective. However, more active and durable catalysts are required for this purpose. Herein, polyaniline (PANI)-derived carbon materials were obtained to boost the oxygen reduction reaction (ORR) and, consequently, the performance of a primary ZAB. The developed porous N-doped carbon (NDC) materials were engineered by varying the polymerization time and calcination temperature (500–900 °C). SEM micrographs and BET surface areas showed that the polymerization of aniline under cold conditions (5 °C) at 6, 8, or 24 h did not have a significant effect on the morphology or surface area. The fibrous structure of PANI was engineered by temperature, resulting in a progressive increase in the surface area until a three-dimensional porous structure was achieved at 900 °C with the highest area of 601.9 m<sup>2</sup> g<sup>−1</sup>. The surface doping of nitrogen species shifted from PANI-rich N species to enriched graphitic N from 12.69 % (500 °C) to 24.26 % at 900 °C. The NDC 900 °C presented a voltage of 1.4 V and power density of 56 mW cm<sup>−2</sup> (only 7 mW cm<sup>−2</sup> lower than that of Pt/C). The results demonstrate that this material is an excellent candidate for high-performance primary ZABs.</p>","PeriodicalId":54339,"journal":{"name":"ChemNanoMat","volume":"10 10","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemNanoMat","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cnma.202400361","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Zinc-air batteries (ZABs) with metal-free cathodes are considered environmentally friendly and cost-effective. However, more active and durable catalysts are required for this purpose. Herein, polyaniline (PANI)-derived carbon materials were obtained to boost the oxygen reduction reaction (ORR) and, consequently, the performance of a primary ZAB. The developed porous N-doped carbon (NDC) materials were engineered by varying the polymerization time and calcination temperature (500–900 °C). SEM micrographs and BET surface areas showed that the polymerization of aniline under cold conditions (5 °C) at 6, 8, or 24 h did not have a significant effect on the morphology or surface area. The fibrous structure of PANI was engineered by temperature, resulting in a progressive increase in the surface area until a three-dimensional porous structure was achieved at 900 °C with the highest area of 601.9 m2 g−1. The surface doping of nitrogen species shifted from PANI-rich N species to enriched graphitic N from 12.69 % (500 °C) to 24.26 % at 900 °C. The NDC 900 °C presented a voltage of 1.4 V and power density of 56 mW cm−2 (only 7 mW cm−2 lower than that of Pt/C). The results demonstrate that this material is an excellent candidate for high-performance primary ZABs.
ChemNanoMatEnergy-Energy Engineering and Power Technology
CiteScore
6.10
自引率
2.60%
发文量
236
期刊介绍:
ChemNanoMat is a new journal published in close cooperation with the teams of Angewandte Chemie and Advanced Materials, and is the new sister journal to Chemistry—An Asian Journal.