电容去离子
结晶度
无定形固体
材料科学
电极
化学工程
海水淡化
层状结构
相(物质)
纳米技术
膜
电化学
化学
复合材料
结晶学
有机化学
生物化学
工程类
物理化学
作者
Jie Jin,Man Li,Meng‐Ting Tang,Yang Li,Yangyang Liu,Hui Cao,Feihu Li
标识
DOI:10.1021/acssuschemeng.0c04101
摘要
Hybrid capacitive deionization (HCDI) is an emerging and promising technology for water desalination and has been extensively explored in recent years. Designing a structure-tailorable electrode material has been proved to be a valid strategy for achieving a higher salt adsorption capacity (SAC). In this study, MnO2 materials with tailorable phase compositions and crystallinities were prepared hydrothermally and then evaluated as electrodes for removal of ions from a NaCl solution in a membrane-free HCDI cell. MnO2 electrode materials tested in the HCDI system include poorly crystalline δ-MnO2 along with abundant amorphous phases (MnO2-1h); crystalline δ-MnO2 with plentiful amorphous MnO2 (MnO2-2h); MnO2 mixtures of α-, δ-, and amorphous MnO2 (MnO2-5h); and α-MnO2 nanowires with minor amorphous MnO2 (MnO2-12h). Our results revealed that the phase composition and the crystallinity of MnO2 materials govern their specific capacitances and thus the SAC values. When the cell voltage is 1.2 V, the lamellar-structured poorly crystalline MnO2-1h electrode with the lowest crystallinity demonstrates the highest SACs of 13.84 mg g–1 in 100 mg L–1 NaCl (1.71 mM) and 21.32 mg g–1 in 500 mg L–1 NaCl (8.56 mM) solutions, respectively. The desalination efficiencies of the MnO2−1h electrode are remarkable and much greater than other MnO2-based electrodes under similar conditions (e.g., NaCl concentrations, cell voltage, etc.). This study sheds light on the significance of understanding the fundamentals of both the phase composition and crystallinity in defining the desalination performance of MnO2 electrodes.
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