Biomass-based N/P co-doped hierarchical porous carbon fabricated by a facile dual physico-chemical activation strategy for efficient capacitive deionization

电容去离子 材料科学 化学工程 比表面积 杂原子 热解 海水淡化 碳纤维 碳酸钾 超级电容器 纳米技术 电化学 电极 化学 有机化学 催化作用 复合材料 物理化学 工程类 复合数 戒指(化学) 生物化学
作者
Hua Qiang,Mingxing Shi,Fengyun Wang,Mingzhu Xia
出处
期刊:Separation and Purification Technology [Elsevier]
卷期号:333: 125915-125915 被引量:45
标识
DOI:10.1016/j.seppur.2023.125915
摘要

The preparation of heteroatom-doped hierarchical porous carbons (HPCs) possessing both high-performance and cost-effective is advantageous for the advancement of capacitive deionization (CDI). Biomass, which is abundant and inexpensive, has been widely utilized as a precursor for carbon electrodes. However, the simple pyrolysis of a single biomass typically leads to insufficient porosity with narrow surface area, along with poor wettability and conductivity, thereby resulting in limited desalination performance. Therefore, we employ ammonium dihydrogen phosphate (NH4H2PO4) and potassium carbonate (K2CO3) as chemical and physical activators, respectively, to co-activate lotus petiole (LP) for the preparation of N/P co-doped hierarchical porous carbon (NPHPC). In comparison with conventional single K2CO3 activation, NPHPC prepared through dual physico-chemical activation exhibits exceptional specific surface area (SBET, 2170.00 m2/g), excellent pore volume (Vpore, 1.16 cm3/g), outstanding mesoporosity (Vmeso/Vpore, 72.41 %), superior hydrophilic performance (contact angle: 39°), high specific capacitance (221.86F/g), moderate N-doping (3.1 %) and P-doping (0.4 %). When assembled for desalination, the synthesized materials demonstrate a fabulous electroadsorption capacity of 21.85 mg/g together with notable cycling stability, highlighting their excellent application prospects. In summary, this work presents innovative ideas in proposing a facile synthesis of high-performance heteroatom-doped HPCs for CDI desalination.
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