Abstract:A natural self-regeneration step for urea derived graphitic carbon nitride with platinum nanoparticles is found by simply opening the system to air in the dark under ambient conditions, following its solar-driven hydrogen production. The produced peroxides deactivate the graphitic carbon nitride. Release of weakly bound peroxides on the polymeric semiconductor surface is a crucial process for regeneration.
“…[ 12 ] In addition to the poor photocatalytic activity, the g-C 3 N 4 has demonstrated a two-electron favored charge exchange in the electroreduction of O 2 , [ 13 ] as well as the distinct H 2 O 2 generation during the photocatalytic H 2 generation. [ 5 ] Herein, we report a novel carbon nitride nanowire bundles (CN NWBs) evolved from g-C 3 N 4 sheets that undergo processes of iodine doping, oxidative cleavage into carbon nitride quantum dots (CNQDs), and restacking of the CNQDs. The resultant restacked CN NWBs could extend the light-absorption ability to a broader wavelength region due to structural distortion and enhance charge separation by the 1D structure compared with that of individual CNQDs; therefore a simple restacking process could induce a stable and novel secondary structure with a narrower bandgap.…”
A stepwise four‐electron reaction significantly alleviates the thermodynamics reaction barrier for overall water splitting. Regenerated 1D carbon nitride nanowire bundles from tailoring and reassembly of 2D g‐C3N4 produce novel physicochemical and optoelectronic properties, which well realize the stepwise four‐electron reaction along with a quantum efficiency of 5.2‰ at 420 nm.
“…[ 12 ] In addition to the poor photocatalytic activity, the g-C 3 N 4 has demonstrated a two-electron favored charge exchange in the electroreduction of O 2 , [ 13 ] as well as the distinct H 2 O 2 generation during the photocatalytic H 2 generation. [ 5 ] Herein, we report a novel carbon nitride nanowire bundles (CN NWBs) evolved from g-C 3 N 4 sheets that undergo processes of iodine doping, oxidative cleavage into carbon nitride quantum dots (CNQDs), and restacking of the CNQDs. The resultant restacked CN NWBs could extend the light-absorption ability to a broader wavelength region due to structural distortion and enhance charge separation by the 1D structure compared with that of individual CNQDs; therefore a simple restacking process could induce a stable and novel secondary structure with a narrower bandgap.…”
A stepwise four‐electron reaction significantly alleviates the thermodynamics reaction barrier for overall water splitting. Regenerated 1D carbon nitride nanowire bundles from tailoring and reassembly of 2D g‐C3N4 produce novel physicochemical and optoelectronic properties, which well realize the stepwise four‐electron reaction along with a quantum efficiency of 5.2‰ at 420 nm.
“…Because nanostructural g-C 3 N 4 possesses larger number of active sites and exhibits smaller mass transfer resistance in the course of photocatalytic reaction compared with bulk g-C 3 N 4 . Other researchers tried to deposit noble metals on the surface of g-C 3 N 4 for capturing photoexcited electrons, thereby decreasing the photogenerated electron (e − )-hole (h + ) pair recombination probability [21][22][23]. Unfortunately, some problems exist in the above modification methods: first, the procedure for the nanostructure design is complex and toxic solvents are used in the preparation process.…”
“…Since then g-C 3 N 4 has attracted intense interest due to its high thermal stability and low product cost [19,20]. g-C 3 N 4 was reported to have a band gap of about 2.7 eV, and can absorb visible light up to 460 nm [18,21].…”
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