{"title":"通过熔融碱活化优化碳化废咖啡渣的表面特性和孔隙率,以增强锌超级电池的性能","authors":"Ishioma Laurene Egun , Yang Hou , Zhengfei Chen","doi":"10.1016/j.ces.2025.121404","DOIUrl":null,"url":null,"abstract":"<div><div>Zinc Supercapatteries (ZnSCs) are promising, low-cost and environmentally friendly electrochemical energy storage devices, with biomass-derived carbon showing promising results as its positrode active material. However, achieving sustainable biomass-derived carbon via a simple, single-stage and low-temperature process with properties for optimum electrochemical performance is still a challenge. In this study, we show that ultramicroporous and self-doped carbon which are critical electrode properties can be obtained from wet waste coffee grounds via a single-stage thermal process termed molten base carbonization and activation. The process integrates carbonization, in-situ activation and self-doping in one thermal step, driven by the catalytic reactivity of intercalated potassium ion within various components. Temperature control during the process resulted to changes in the microstructure, hierarchical porosity, oxygen and nitrogen functionalities affecting electrochemical performance. The carbon obtained at 700 °C (CGZ-700) as positive electrode active material in Zinc supercapattery achieved specific capacity of 361 mAh g<sup>−1</sup>, specific capacitance of 204F g<sup>−1</sup> at 0.1 A g<sup>−1</sup>, alongside a specific energy and power of 91.99 Wh kg<sup>−1</sup> and 89.99 W kg<sup>−1</sup>. At 1.0 A g<sup>−1</sup>, it achieved a coulombic efficiency of 99.8 % and 78 % capacity retention after 10,000 cycles. This study offers a facile, low temperature single-stage thermal conversion process for low-cost waste biomass, advancing the application of waste-derived carbon in ZnSCs and sustainable energy storage devices.</div></div>","PeriodicalId":271,"journal":{"name":"Chemical Engineering Science","volume":"308 ","pages":"Article 121404"},"PeriodicalIF":4.3000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimizing surface properties and porosity of carbonized waste coffee grounds via molten base activation for enhanced zinc supercapattery performance\",\"authors\":\"Ishioma Laurene Egun , Yang Hou , Zhengfei Chen\",\"doi\":\"10.1016/j.ces.2025.121404\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Zinc Supercapatteries (ZnSCs) are promising, low-cost and environmentally friendly electrochemical energy storage devices, with biomass-derived carbon showing promising results as its positrode active material. However, achieving sustainable biomass-derived carbon via a simple, single-stage and low-temperature process with properties for optimum electrochemical performance is still a challenge. In this study, we show that ultramicroporous and self-doped carbon which are critical electrode properties can be obtained from wet waste coffee grounds via a single-stage thermal process termed molten base carbonization and activation. The process integrates carbonization, in-situ activation and self-doping in one thermal step, driven by the catalytic reactivity of intercalated potassium ion within various components. Temperature control during the process resulted to changes in the microstructure, hierarchical porosity, oxygen and nitrogen functionalities affecting electrochemical performance. The carbon obtained at 700 °C (CGZ-700) as positive electrode active material in Zinc supercapattery achieved specific capacity of 361 mAh g<sup>−1</sup>, specific capacitance of 204F g<sup>−1</sup> at 0.1 A g<sup>−1</sup>, alongside a specific energy and power of 91.99 Wh kg<sup>−1</sup> and 89.99 W kg<sup>−1</sup>. At 1.0 A g<sup>−1</sup>, it achieved a coulombic efficiency of 99.8 % and 78 % capacity retention after 10,000 cycles. This study offers a facile, low temperature single-stage thermal conversion process for low-cost waste biomass, advancing the application of waste-derived carbon in ZnSCs and sustainable energy storage devices.</div></div>\",\"PeriodicalId\":271,\"journal\":{\"name\":\"Chemical Engineering Science\",\"volume\":\"308 \",\"pages\":\"Article 121404\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Engineering Science\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0009250925002271\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Engineering Science","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009250925002271","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/19 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
摘要
锌超级电容器(ZnSCs)是一种极具发展前景的低成本、环保的电化学储能装置,其正极活性材料是生物质碳。然而,通过简单、单阶段和低温工艺实现可持续的生物质衍生碳,并具有最佳的电化学性能仍然是一个挑战。在这项研究中,我们证明了超微孔和自掺杂碳是关键的电极性能,可以通过被称为熔融碱碳化和活化的单阶段热过程从湿的废咖啡渣中获得。该工艺将炭化、原位活化和自掺杂在一个热步骤中,由插层钾离子在各种成分中的催化反应性驱动。过程中的温度控制会导致微观结构、分层孔隙度、氧和氮功能的变化,从而影响电化学性能。在700 °C (cgc -700)下获得的碳作为锌超级电池的正极活性材料,比容量为361 mAh g−1,比电容为204F g−1,比能量和比功率分别为91.99 Wh kg−1和89.99 W kg−1。在1.0 A g−1时,库仑效率为99.8 %,循环10000次后容量保持率为78 %。本研究为低成本的废生物质提供了一种简单、低温的单阶段热转化工艺,推进了废碳在ZnSCs和可持续储能装置中的应用。
Optimizing surface properties and porosity of carbonized waste coffee grounds via molten base activation for enhanced zinc supercapattery performance
Zinc Supercapatteries (ZnSCs) are promising, low-cost and environmentally friendly electrochemical energy storage devices, with biomass-derived carbon showing promising results as its positrode active material. However, achieving sustainable biomass-derived carbon via a simple, single-stage and low-temperature process with properties for optimum electrochemical performance is still a challenge. In this study, we show that ultramicroporous and self-doped carbon which are critical electrode properties can be obtained from wet waste coffee grounds via a single-stage thermal process termed molten base carbonization and activation. The process integrates carbonization, in-situ activation and self-doping in one thermal step, driven by the catalytic reactivity of intercalated potassium ion within various components. Temperature control during the process resulted to changes in the microstructure, hierarchical porosity, oxygen and nitrogen functionalities affecting electrochemical performance. The carbon obtained at 700 °C (CGZ-700) as positive electrode active material in Zinc supercapattery achieved specific capacity of 361 mAh g−1, specific capacitance of 204F g−1 at 0.1 A g−1, alongside a specific energy and power of 91.99 Wh kg−1 and 89.99 W kg−1. At 1.0 A g−1, it achieved a coulombic efficiency of 99.8 % and 78 % capacity retention after 10,000 cycles. This study offers a facile, low temperature single-stage thermal conversion process for low-cost waste biomass, advancing the application of waste-derived carbon in ZnSCs and sustainable energy storage devices.
期刊介绍:
Chemical engineering enables the transformation of natural resources and energy into useful products for society. It draws on and applies natural sciences, mathematics and economics, and has developed fundamental engineering science that underpins the discipline.
Chemical Engineering Science (CES) has been publishing papers on the fundamentals of chemical engineering since 1951. CES is the platform where the most significant advances in the discipline have ever since been published. Chemical Engineering Science has accompanied and sustained chemical engineering through its development into the vibrant and broad scientific discipline it is today.