Abstract:A facile route to synthesize hydrophilically or hydrophobically grafted graphitic carbon nitride (g-CN) is reported. For this purpose, functionalized olefinic molecules with a low polymerization tendency are utilized for grafting onto the surface to preserve the features of g-CN while improving its dispersibility. One-pot, visible light-induced grafting yields highly dispersible g-CNs either in aqueous or organic media. Moreover, functional groups such as amines can be introduced, which yields pH-dependent dis… Show more
“…Sulfonic acid functionalized g‐CN (g‐CN‐AHPA) was synthesized via cyanuric acid‐melamine complex and surface modification as reported in literature . Modification of g‐CN with AHPA was confirmed via elemental analysis and zeta potential (Table S1, Supporting Information), as well as transmission electron microscopy (Figure S1, Supporting Information), energy‐dispersive X‐ray spectroscopy mapping in scanning electron microscopy (SEM) (Figure S2, Supporting Information) and spectroscopy (Figure S3, Supporting Information).…”
Section: Methodsmentioning
confidence: 95%
“…It was shown that g‐CN sheets act as reinforcer and photoinitiator in radical mediated hydrogel formation with surface charge being one of the important parameters regarding hydrogel strength . Our group recently developed a one pot grafting method to anchor functional groups on the surface of g‐CN, showing excellent dispersions in aqueous and organic media . In such a way, 3‐allyloxy‐2‐hydroxy‐1‐propanesulfonic acid (AHPA) groups can be grafted onto the g‐CN surface (g‐CN‐AHPA) for enhanced dispersibility in water and lower surface zeta potential, which may lead to the formation of strong hydrogels.…”
Extremely compressible hydrogels are fabricated in one pot via sulfonic‐acid‐modified graphitic carbon nitride (g‐CN‐AHPA) as a visible light photoinitiator and reinforcer. The hydrogels show unusual compressibility upon applied stress up to 12 MPa, presenting temporary physical deformation, and remain undamaged after stress removal despite their high water content (90 wt%). Cyclic compressibility proves the fatigue resistance of the covalently and electrostatically reinforced system that possesses tissue adhesive properties, shock resistance, cut resistance, and little to no toxicity.
“…Sulfonic acid functionalized g‐CN (g‐CN‐AHPA) was synthesized via cyanuric acid‐melamine complex and surface modification as reported in literature . Modification of g‐CN with AHPA was confirmed via elemental analysis and zeta potential (Table S1, Supporting Information), as well as transmission electron microscopy (Figure S1, Supporting Information), energy‐dispersive X‐ray spectroscopy mapping in scanning electron microscopy (SEM) (Figure S2, Supporting Information) and spectroscopy (Figure S3, Supporting Information).…”
Section: Methodsmentioning
confidence: 95%
“…It was shown that g‐CN sheets act as reinforcer and photoinitiator in radical mediated hydrogel formation with surface charge being one of the important parameters regarding hydrogel strength . Our group recently developed a one pot grafting method to anchor functional groups on the surface of g‐CN, showing excellent dispersions in aqueous and organic media . In such a way, 3‐allyloxy‐2‐hydroxy‐1‐propanesulfonic acid (AHPA) groups can be grafted onto the g‐CN surface (g‐CN‐AHPA) for enhanced dispersibility in water and lower surface zeta potential, which may lead to the formation of strong hydrogels.…”
Extremely compressible hydrogels are fabricated in one pot via sulfonic‐acid‐modified graphitic carbon nitride (g‐CN‐AHPA) as a visible light photoinitiator and reinforcer. The hydrogels show unusual compressibility upon applied stress up to 12 MPa, presenting temporary physical deformation, and remain undamaged after stress removal despite their high water content (90 wt%). Cyclic compressibility proves the fatigue resistance of the covalently and electrostatically reinforced system that possesses tissue adhesive properties, shock resistance, cut resistance, and little to no toxicity.
“…In aktuellen Arbeiten wurden auch kohlenstoffbasierte Nanomaterialien wie graphitisches Kohlenstoffnitrid (g-C 3 N 4 )und C-Dots (CDs) in photobiokatalytischen Anwendungen eingesetzt. [38,39] C-Dots sind quasi-sphärische Partikel mit einem Durchmesser von weniger als 10 nm. [36] g-C 3 N 4 ist ein metallfreier polymerer Photokatalysator mit starker Absorption im Bereich sichtbaren Lichts und einer Bandlücke von etwa 2.7 eV.…”
Biokatalytische Umsetzungen rücken aufgrund der Vielfältigkeit der Enzyme, ihrer hohen katalytischen Aktivität und Spezifität und der milden Reaktionsbedingungen zunehmend in den Fokus einer “grünen” Synthesechemie. Der Ansatz, Sonnenenergie durch Kombination von Photokatalyse und Biokatalyse für die chemische Synthese nutzbar zu machen, bietet eine Möglichkeit, diesen “grünen” Prozess noch nachhaltiger zu gestalten. Oxidoreduktasen katalysieren die Umsetzung verschiedener Substrate durch den Austausch von Elektronen am aktiven Zentrum des Enzyms, meist mithilfe von Elektronenmediatoren. Aktuelle Fortschritte auf diesem Gebiet zeigen, dass photoinduzierter Elektronentransfer unter Einsatz organischer (oder anorganischer) Photosensibilisatoren ein breites Spektrum von Redoxenzymen aktivieren kann, welche in Folge wichtige Brennstoffe liefern (z. B. H2‐Bildung, CO2‐Reduktion) oder synthetisch relevante Reduktionen vermitteln (z. B. asymmetrische Reduktionen, Oxygenierungen, Hydroxylierungen, Epoxidierungen, Bayer‐Villiger‐Oxidation). Dieser Aufsatz gibt einen Überblick über aktuelle Entwicklungen auf dem Gebiet der Photoaktivierung von Redoxenzymen mittels direkter oder indirekter Übertragung photoinduzierter Elektronen.
“…The reason lies on the poor dispersibility of most CNs in common solvents, which make them almost non‐processable for (photo)electronic applications . Without ignoring the great progress in this field, mainly by the introduction of new exfoliation methods, the improvement of their dispersibility and more specifically allowing the easy and scalable preparation of well‐dispersed CN materials with enhanced and tunable electronic and light‐harvesting properties is still highly required …”
A general and straightforward synthesis of a series of solution‐processable carbon nitride polymers is described with excellent and tunable optical and electronic properties. The high dispersibility of carbon nitride polymers functionalized with polycyclic aromatic hydrocarbons (PAH‐CNs) in common solvents permits their facile processing into thin films utilizing routine methods such as spin‐coating and drop‐casting. Moreover, altering the PAH group within the CN scaffold enables great tunability of their optical and electronic properties as well as a range of functionalities. This is illustrated by a variety of photoelectrochemical properties, electropolymerization ability, and photoswitching properties for the different PAH‐CNs. The easy processing and tunable properties allow the construction of advanced electronic structures, such as a heterojunction, which significantly improves the photoelectrochemical performance. The versatility of this solution‐processable platform holds promise for the applicability of CNs in new photoelectronic devices.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.