2016
DOI: 10.1016/j.carbon.2016.01.027
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Engineering monomer structure of carbon nitride for the effective and mild photooxidation reaction

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Cited by 68 publications
(35 citation statements)
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“…Latterly, various types of monomer precursors with cyano and/or amino groups have been developed for integrating organic molecules with different functional groups into the CN frameworks. 919 However, after modification by the organic molecular doping method, the valence band (VB) position of g-C 3 N 4 was sharply shifted toward the negative potential position, which was detrimental to its applications in the organic pollutant degradation by dramatically decreasing the oxidizability of the organic-molecule-doped g-C 3 N 4 . 19,29 Therefore, it is highly desired to develop a novel strategy to maintain or enhance the reducibility and oxidizability of the organic-molecule-doped g-C 3 N 4 .…”
Section: Introductionmentioning
confidence: 99%
“…Latterly, various types of monomer precursors with cyano and/or amino groups have been developed for integrating organic molecules with different functional groups into the CN frameworks. 919 However, after modification by the organic molecular doping method, the valence band (VB) position of g-C 3 N 4 was sharply shifted toward the negative potential position, which was detrimental to its applications in the organic pollutant degradation by dramatically decreasing the oxidizability of the organic-molecule-doped g-C 3 N 4 . 19,29 Therefore, it is highly desired to develop a novel strategy to maintain or enhance the reducibility and oxidizability of the organic-molecule-doped g-C 3 N 4 .…”
Section: Introductionmentioning
confidence: 99%
“…Since Wang et al reported graphitic carbon nitride( g-C 3 N 4 ), am etal-free polymer semiconductor that is able to produce hydrogen or oxygen by splitting water under visible-light irradiation, [17] g-C 3 N 4 has attracted more and more attention for its application in supercapacitors, [18] lithiumion batteries, [19] photodegradation of pollutants, [20,21] and especially in photocatalytic hydrogen production. [26] Up to now,s everal approaches have been explored to improve the visible-light utilization of g-C 3 N 4 to achieve high photocatalytic activity,i ncluding doping with metal and/or nonmetal ions, [27][28][29][30][31][32] construction of heterojunctions with other semiconductors, [20,21,25,[33][34][35] copolymerization with organic molecules, [35][36][37][38][39] modification with carbon materials, [40][41][42] co-catalyst deposition, [43,44] thin-film fabrication, [45] and photosensitization with dyes. However, pristine g-C 3 N 4 exhibits limited photocatalytic activity owing to its small specific surface area, poor visible-light utilization, and fast recombination of photogenerated electrons and holes.…”
Section: Introductionmentioning
confidence: 99%
“…Up to now, several approaches have been explored to improve the visible‐light utilization of g‐C 3 N 4 to achieve high photocatalytic activity, including doping with metal and/or nonmetal ions, construction of heterojunctions with other semiconductors, copolymerization with organic molecules, modification with carbon materials, co‐catalyst deposition, thin‐film fabrication, and photosensitization with dyes . Among these methods, nonmetal doping has been demonstrated to be an effective way to incorporate external impurities into g‐C 3 N 4 to modulate its electronic structure to achieve high photocatalytic performance.…”
Section: Introductionmentioning
confidence: 99%
“…Similar to S,N-codoped photocatalysts, the N,P-dual-doped carbonaceousp hotocatalysts, also called P-doped g-C 3 N 4 ,h ave also gained great interest. [284][285][286][287][288][289][304][305][306][307][308] From Ta ble7,t he copolymerization of N-containing precursor like melamine, dicyandiamide or guanidiniumh ydrochloridew ith the Pp recursor like 1-butyl-3-methylimidazolium hexa fluorophosphate (BMIMPF 6 ), hydroxyethylide dediphosphonic acid (HEDP) or 2aminoethyl phosphonic acid (AEP) is ag eneral method for pre-aring P-doped g-C 3 N 4 . [284][285][286] In addition, the combination methods including the coploymerization followed by exfoliation, [287] milling followed by annealing, [288] preorganization followed by thermal condensation, [289] were employed to fabricating P-doped g-C 3 N 4 nano/micro structuresw ith diverse morphologies and prysicochemical properties.…”
Section: Nitrogen and Phosphorus Dual-doped Carbonaceous Photocatalystsmentioning
confidence: 99%
“…Similar to S, N ‐codoped photocatalysts, the N,P‐dual‐doped carbonaceous photocatalysts, also called P‐doped g‐C 3 N 4 , have also gained great interest . From Table , the copolymerization of N ‐containing precursor like melamine, dicyandiamide or guanidinium hydrochloride with the P precursor like 1‐butyl‐3‐methylimidazolium hexa fluorophosphate (BMIMPF 6 ), hydroxyethylide dediphosphonic acid (HEDP) or 2‐aminoethyl phosphonic acid (AEP) is a general method for prearing P‐doped g‐C 3 N 4 .…”
Section: Heteroatoms Co‐doped Carbonaceous Photocatalystsmentioning
confidence: 99%