A dual-acetate synchronous catalysis-activation strategy towards regulable porous graphitic carbon for high-energy supercapacitor with acetate water-in-salt electrolyte

超级电容器 电解质 化学工程 碳纤维 无机化学 材料科学 电化学 活性炭 水溶液 储能 盐(化学) 化学 电极 有机化学 复合材料 冶金 功率(物理) 物理 物理化学 吸附 量子力学 复合数 工程类
作者
Huanxi Liao,Longsheng Zhong,Hejun Zeng,Yanhe Xiao,Baochang Cheng,Shuijin Lei
出处
期刊:Carbon [Elsevier]
卷期号:213: 118305-118305 被引量:12
标识
DOI:10.1016/j.carbon.2023.118305
摘要

Supercapacitors are one of the most extensively studied energy storage devices due to their many unique advantages. The design of electrode material and electrolyte is the key to building high-performance supercapacitors. In this work, high-energy aqueous supercapacitors are constructed by optimizing these two factors. On the one hand, a dual-acetate (nickel/potassium acetates) synchronous catalysis-activation strategy is developed for the first time to prepare porous graphitic carbon from commercial super absorbent polymer as electrode material. Compared with the porous carbon activated by potassium acetate alone and the graphitic carbon catalyzed by nickel acetate alone, the porous graphitic carbon shows much more remarkable electrochemical performance. On the other hand, the impacts of water-in-salt and salt-in-water electrolytes of aqueous potassium acetate on energy storage properties of supercapacitors are investigated comparatively. The water-in-salt electrolyte of 22 M potassium acetate has a significant effect in broadening voltage window up to 2.95 V. When the operating voltage window is extended from 1.6 to 2.2 V, the energy density can be increased from 17.1 to 40.6 Wh kg−1. Moreover, both the porous graphitic carbon electrode and potassium acetate water-in-salt electrolyte are conducive to the slow self-discharge capability.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI5应助SCI采纳,获得10
刚刚
dling02完成签到 ,获得积分10
刚刚
刚刚
是天使呢完成签到,获得积分10
刚刚
1秒前
1秒前
内向秋寒发布了新的文献求助10
1秒前
cc发布了新的文献求助10
1秒前
ding应助zhui采纳,获得10
2秒前
drwang120完成签到 ,获得积分10
2秒前
坨坨西州完成签到,获得积分10
3秒前
海绵体宝宝应助Louise采纳,获得20
3秒前
小马甲应助lichaoyes采纳,获得10
3秒前
3秒前
4秒前
4秒前
坨坨西州发布了新的文献求助10
5秒前
彬彬发布了新的文献求助10
5秒前
大模型应助Abao采纳,获得10
5秒前
sfw驳回了苏照杭应助
6秒前
dingdong发布了新的文献求助10
6秒前
别拖延了要毕业啊完成签到,获得积分10
7秒前
7秒前
7秒前
Rrr发布了新的文献求助10
7秒前
dingdong发布了新的文献求助10
8秒前
8秒前
9秒前
9秒前
9秒前
10秒前
yuan发布了新的文献求助10
10秒前
11秒前
cc完成签到,获得积分10
11秒前
11秒前
11秒前
12秒前
12秒前
一一发布了新的文献求助10
12秒前
领导范儿应助Chridy采纳,获得10
12秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Social media impact on athlete mental health: #RealityCheck 1020
Ensartinib (Ensacove) for Non-Small Cell Lung Cancer 1000
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Bacterial collagenases and their clinical applications 800
El viaje de una vida: Memorias de María Lecea 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3527849
求助须知:如何正确求助?哪些是违规求助? 3107938
关于积分的说明 9287239
捐赠科研通 2805706
什么是DOI,文献DOI怎么找? 1540033
邀请新用户注册赠送积分活动 716893
科研通“疑难数据库(出版商)”最低求助积分说明 709794