Yen-Zen Wang , Ko-Shan Ho , Yu-Chang Huang , Yu-Wei Cheng , Chia-Long Miao , Pei-Ying Yeh
{"title":"煅烧共螯合、亚胺交联壳聚糖作为阴离子交换膜燃料电池的ORR催化剂","authors":"Yen-Zen Wang , Ko-Shan Ho , Yu-Chang Huang , Yu-Wei Cheng , Chia-Long Miao , Pei-Ying Yeh","doi":"10.1016/j.cartre.2024.100444","DOIUrl":null,"url":null,"abstract":"<div><div>Cobalt-chelating imine-crosslinked chitosan (Co-ICCA) is synthesized via Schiff base condensation of terephthalaldehyde and chitosan in the presence of cobalt chloride. Co-ICCA transforms into Co, N-co-doped carbon cathode catalysts (Co-N-Cs) upon calcination. The successful synthesis is confirmed using Fourier Transform Infrared Spectroscopy. The porous morphologies of the calcined Co-ICCA are characterized by transmission electron microscopy, high-resolution transmission electron microscopy, and field-emission scanning electron microscopy. The Co-N-Cs exhibit a high specific surface area (433 m²/g) and porosity, as analyzed by a BET analyzer. X-ray diffraction patterns reveal sharp graphite diffraction peaks and feature peaks of Co-crystal with an FCC lattice when the calcination temperature exceeds 800 °C, indicating high crystallinity.</div><div>Meanwhile, Raman spectra show a higher G-band intensity compared to the D-band. The performance of Co-N-Cs as cathode catalysts, particularly in the oxygen reduction reaction, is evaluated through current-voltage and linear sweep voltammetry curves and compared to commercial Pt/C catalysts. Single-cell using the Co-N-C catalyst as the cathode reaches a high maximum power density of 221 mW cm<sup>-2</sup>, close to the 285 mW cm<sup>-</sup>² achieved with Pt/C as the cathode catalyst.</div></div>","PeriodicalId":52629,"journal":{"name":"Carbon Trends","volume":"18 ","pages":"Article 100444"},"PeriodicalIF":3.1000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Calcined Co-chelating, imine-crosslinking chitosan as the ORR catalyst of an anion exchange membrane fuel cell\",\"authors\":\"Yen-Zen Wang , Ko-Shan Ho , Yu-Chang Huang , Yu-Wei Cheng , Chia-Long Miao , Pei-Ying Yeh\",\"doi\":\"10.1016/j.cartre.2024.100444\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cobalt-chelating imine-crosslinked chitosan (Co-ICCA) is synthesized via Schiff base condensation of terephthalaldehyde and chitosan in the presence of cobalt chloride. Co-ICCA transforms into Co, N-co-doped carbon cathode catalysts (Co-N-Cs) upon calcination. The successful synthesis is confirmed using Fourier Transform Infrared Spectroscopy. The porous morphologies of the calcined Co-ICCA are characterized by transmission electron microscopy, high-resolution transmission electron microscopy, and field-emission scanning electron microscopy. The Co-N-Cs exhibit a high specific surface area (433 m²/g) and porosity, as analyzed by a BET analyzer. X-ray diffraction patterns reveal sharp graphite diffraction peaks and feature peaks of Co-crystal with an FCC lattice when the calcination temperature exceeds 800 °C, indicating high crystallinity.</div><div>Meanwhile, Raman spectra show a higher G-band intensity compared to the D-band. The performance of Co-N-Cs as cathode catalysts, particularly in the oxygen reduction reaction, is evaluated through current-voltage and linear sweep voltammetry curves and compared to commercial Pt/C catalysts. Single-cell using the Co-N-C catalyst as the cathode reaches a high maximum power density of 221 mW cm<sup>-2</sup>, close to the 285 mW cm<sup>-</sup>² achieved with Pt/C as the cathode catalyst.</div></div>\",\"PeriodicalId\":52629,\"journal\":{\"name\":\"Carbon Trends\",\"volume\":\"18 \",\"pages\":\"Article 100444\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbon Trends\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667056924001238\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Trends","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667056924001238","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Calcined Co-chelating, imine-crosslinking chitosan as the ORR catalyst of an anion exchange membrane fuel cell
Cobalt-chelating imine-crosslinked chitosan (Co-ICCA) is synthesized via Schiff base condensation of terephthalaldehyde and chitosan in the presence of cobalt chloride. Co-ICCA transforms into Co, N-co-doped carbon cathode catalysts (Co-N-Cs) upon calcination. The successful synthesis is confirmed using Fourier Transform Infrared Spectroscopy. The porous morphologies of the calcined Co-ICCA are characterized by transmission electron microscopy, high-resolution transmission electron microscopy, and field-emission scanning electron microscopy. The Co-N-Cs exhibit a high specific surface area (433 m²/g) and porosity, as analyzed by a BET analyzer. X-ray diffraction patterns reveal sharp graphite diffraction peaks and feature peaks of Co-crystal with an FCC lattice when the calcination temperature exceeds 800 °C, indicating high crystallinity.
Meanwhile, Raman spectra show a higher G-band intensity compared to the D-band. The performance of Co-N-Cs as cathode catalysts, particularly in the oxygen reduction reaction, is evaluated through current-voltage and linear sweep voltammetry curves and compared to commercial Pt/C catalysts. Single-cell using the Co-N-C catalyst as the cathode reaches a high maximum power density of 221 mW cm-2, close to the 285 mW cm-² achieved with Pt/C as the cathode catalyst.