2023
DOI: 10.1016/j.ceramint.2022.11.133
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Cu/Cu2O nanoparticles modified Ti3C2 MXene with in-situ formed TiO2-X for detection of hydrogen peroxide

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Cited by 13 publications
(4 citation statements)
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“…Owing to the least conductivity and absence of the synergy effect, CuMgAl LDH/GCE reveals lesser H 2 O 2 reducing capability than that of CuMgAl LDH/Ti 3 C 2 T x -3/GCE. The superb electrocatalytic activity of CuMgAl LDH/Ti 3 C 2 T x -3/GCE might have arisen due to various factors such as (i) superlattice formed by successful insertion of extremely conductive Ti 3 C 2 T x sheets in CuMgAl LDH layers, facilitating fast electron transport; (ii) the superlattice possessing large surface area; (iii) the porous surface of the heterostacked assembly responsible for rapid diffusion of the analyte; (iv) layer-by-layer morphology of Ti 3 C 2 T x and CuMgAl LDH providing more interfacial collaborations at the nanoscale interface; and (v) structural integration of charged nanosheets harvesting a plethora of surface active sites, further improving the redox reactions. ,, In the case of CuMgAl LDH/Ti 3 C 2 T x , the possible electrochemical reactions related to H 2 O 2 can be described as follows , Cu 2 normalO + 2 OH 2 normale 2 CuO + normalH 2 normalO 2 CuO + normalH 2 normalO + 2 normale Cu 2 normalO + 2 OH normalH 2 normalO 2 + 2 normale 2 OH 4 OH 4 normale normalO 2 + normalH <...…”
Section: Resultsmentioning
confidence: 99%
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“…Owing to the least conductivity and absence of the synergy effect, CuMgAl LDH/GCE reveals lesser H 2 O 2 reducing capability than that of CuMgAl LDH/Ti 3 C 2 T x -3/GCE. The superb electrocatalytic activity of CuMgAl LDH/Ti 3 C 2 T x -3/GCE might have arisen due to various factors such as (i) superlattice formed by successful insertion of extremely conductive Ti 3 C 2 T x sheets in CuMgAl LDH layers, facilitating fast electron transport; (ii) the superlattice possessing large surface area; (iii) the porous surface of the heterostacked assembly responsible for rapid diffusion of the analyte; (iv) layer-by-layer morphology of Ti 3 C 2 T x and CuMgAl LDH providing more interfacial collaborations at the nanoscale interface; and (v) structural integration of charged nanosheets harvesting a plethora of surface active sites, further improving the redox reactions. ,, In the case of CuMgAl LDH/Ti 3 C 2 T x , the possible electrochemical reactions related to H 2 O 2 can be described as follows , Cu 2 normalO + 2 OH 2 normale 2 CuO + normalH 2 normalO 2 CuO + normalH 2 normalO + 2 normale Cu 2 normalO + 2 OH normalH 2 normalO 2 + 2 normale 2 OH 4 OH 4 normale normalO 2 + normalH <...…”
Section: Resultsmentioning
confidence: 99%
“…Figure 4B As the amount of Ti 3 C 2 T x is increased more than the transitional ratio, aggregation takes place, which does not support the construction of heterostacked superlattice assembly, resulting in suppressing the charge-transferring channels, further reducing the electrocatalytic ability of CuMgAl LDH/Ti (v) structural integration of charged nanosheets harvesting a plethora of surface active sites, further improving the redox reactions. 22,30,31 In the case of CuMgAl LDH/Ti 3 C 2 T x , the possible electrochemical reactions related to H 2 O 2 can be described as follows 32,33 Cu O 2OH 2e 2CuO H O In this method, we started the assay by adding H 2 O 2 concentration even lower than 0.1 nM and then went on increasing it gradually from 0.05 nM to see the reduction current signal for H 2 O 2 . The detectable H 2 O 2 reduction current signal can be well noticed upon spiking 0.1 nM and 0.2 nM H 2 O 2 concentrations, so this is the real-time LOD.…”
Section: Electrocatalytic Properties Of Cumgal Ldh/ Ti 3 C 2 Tmentioning
confidence: 99%
“…Li et al used Cu-Cu O NPs on Ti C Tx MXene and used it for H O detection. This study can be extended for an MXene-based electrochemical sensor for glucose detection [ 84 ].…”
Section: 2dms In Electrochemical Sensing For Glucose Level In Bloodmentioning
confidence: 99%
“…There is a characteristic peak at Cu 2p 3/2 , belongs to Cu 0 /Cu + at 932.21 eV. There are two characteristic peaks at of Cu 2p 1/2 , [ 17 ] the peak at 953.3 eV belongs to Cu 0 /Cu + and the peak at 957.39 eV belongs to Cu 2+ . The high‐resolution energy spectrum of Ag is shown in Figure 4p, and contains two peaks, Ag 3d 5/2 and Ag 3d 3/2 , [ 18 ] with binding energies of 369.07 eV and 374.98 eV, respectively.…”
Section: Study Of the Physicochemical Propertiesmentioning
confidence: 99%