2020
DOI: 10.1007/s12274-020-3097-x
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A confinement strategy to in-situ prepare a peanut-like N-doped, C-wrapped TiO2 electrode with an enhanced desalination capacity and rate for capacitive deionization

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Cited by 31 publications
(20 citation statements)
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“…Ion intercalation or conversion reactions (charge-transfer materials) enable a much higher desalination capacity than possible for carbon-based electrodes because of the higher charge storage capacity and perm-selectivity; thereby, they enable facile desalination even at high molar strength. Currently, various charge-transfer materials for electrochemical desalination have been reported, such as transition metal oxides (MnO 2 , TiO 2 , V 2 O 5 , and ZnFe 2 O 4 ) [8][9][10][11], Prussian blue analogs (nickel hexacyanoferrate) [12][13][14], polyanionic phosphates (Na 3 V 2 (PO 4 ) 3 , Na 3 Ti 2 (PO 4 ) 3 ) [15][16][17], and two-dimensional materials (MXenes, MoS 2 , and TiS 2 ) [18][19][20][21][22]. Among these materials, metal oxides or hydroxides hold the advantages of easy preparation, facile morphological manipulation, element diversity, and promising desalination performance.…”
Section: Introductionmentioning
confidence: 99%
“…Ion intercalation or conversion reactions (charge-transfer materials) enable a much higher desalination capacity than possible for carbon-based electrodes because of the higher charge storage capacity and perm-selectivity; thereby, they enable facile desalination even at high molar strength. Currently, various charge-transfer materials for electrochemical desalination have been reported, such as transition metal oxides (MnO 2 , TiO 2 , V 2 O 5 , and ZnFe 2 O 4 ) [8][9][10][11], Prussian blue analogs (nickel hexacyanoferrate) [12][13][14], polyanionic phosphates (Na 3 V 2 (PO 4 ) 3 , Na 3 Ti 2 (PO 4 ) 3 ) [15][16][17], and two-dimensional materials (MXenes, MoS 2 , and TiS 2 ) [18][19][20][21][22]. Among these materials, metal oxides or hydroxides hold the advantages of easy preparation, facile morphological manipulation, element diversity, and promising desalination performance.…”
Section: Introductionmentioning
confidence: 99%
“…Liang et al, achieved in situ preparation of N-TiO 2 /C by a one-step hydrothermal reaction. [188] Researchers have also tried strategic experimental approaches to produce TiO 2 [114] Copyright 2017, Wiley-VCH. NPs efficiently contacted with in situ formed g-C 3 N 4 NSs, [187] or RGO, during the development of TiO 2 /C composites.…”
Section: Wwwadvmatde Wwwadvancedsciencenewscommentioning
confidence: 99%
“…Liang et al, achieved in situ preparation of N‐TiO 2 /C by a one‐step hydrothermal reaction. [ 188 ] Researchers have also tried strategic experimental approaches to produce TiO 2 NPs efficiently contacted with in situ formed g‐C 3 N 4 NSs, [ 187 ] or RGO, during the development of TiO 2 /C composites. [ 189 ] As demonstrated in Figure 24b, the TiO 2 /C/g‐C 3 N 4 or TiO 2 /RGO heterojunctions produced outstanding characteristics and enhanced functions.…”
Section: The Chemistry Of Mxene‐derived Oxidesmentioning
confidence: 99%
“…Instead of conventional static electrodes, the flow electrodes possess the several orders of magnitude active materials, which expands the electrosorption capacity dramatically. Most plate-type CDI units only explored the low concentration regime in the range of 20–50 mM NaCl. , Some studies have demonstrated that the FCDI system has the ability to treat the feed solution with a high total dissolved solid (TDS) content up to the level of seawater (∼35 000 mg L –1 ) . As opposed to plate-type CDI, the carbon slurry from the anodic and cathodic chambers is mixed in the electrode reservoir for in situ regeneration of the flow electrode, obtaining pseudoinfinite electrosorption capacity and continuous desalination without intermittent regeneration.…”
Section: Introductionmentioning
confidence: 99%