“…CB [6], which could protect alloy NPs against agglomeration and overgrowth, contributes to more uniform alloy NPs distribution in smaller sizes for different alloy compositions by steric hindrance and charge restriction. 29,32 In the inset in Figure 1b, the interplanar spacing of the CB[6]-Cu 0.33 Ir 0.67 alloy measured from the HR-TEM image is 0.21 nm, which is consistent with the lattice spacing of CuIr {111} facets. The energy dispersive X-ray spectroscopy (EDS) mapping profile (Figures 1f and 1g Next, the OER catalytic activity of all the catalysts is measured by linear sweep voltammetry (LSV) in O 2 -saturated 0.5 M H 2 SO 4 aqueous solution.…”
supporting
confidence: 63%
“…Additionally, the size measurements suggest that the series of CB[6]-Cu x Ir (1– x ) hybrids in different alloy compositions present similar sizes of ∼2.0 ± 0.3 nm (Figures S3, S4, and S5 in the Supporting Information). CB[6], which could protect alloy NPs against agglomeration and overgrowth, contributes to more uniform alloy NPs distribution in smaller sizes for different alloy compositions by steric hindrance and charge restriction. , In the inset in Figure b, the interplanar spacing of the CB[6]-Cu 0.33 Ir 0.67 alloy measured from the HR-TEM image is 0.21 nm, which is consistent with the lattice spacing of CuIr {111} facets. The energy dispersive X-ray spectroscopy (EDS) mapping profile (Figures f and g) shows that the bimetallic Cu–Ir NPs are composed of elements Cu and Ir.…”
Designing applicable high activity over long-term operation Ir-based alloy oxygen evolution reaction (OER) catalysts plays an important role in the development of the water-splitting process under acidic conditions. Herein, we report that cucurbit[6]uril-supported copper−iridium alloy (CB[6]-CuIr) hybrid with the enhancement of activity and stability for OER. The CB[6]-Cu 0.33 Ir 0.67 shows a current density of 11.68 mA/cm 2 , which is 8.4 times greater than that of Ir black at η = 280 mV. CB[6]-Cu 0.33 Ir 0.67 exhibits superior stability without activity loss after 10 h of continuous operation at 10 mA/cm 2 , while the CuIr alloy stabilized by carbon or polyvinylpyrrolidone is deactivated within 1 and 4 h, respectively. X-ray absorption fine structure (XAFS) and electron energy loss spectroscopy (EELS) confirm the interaction between the Cu 0.33 Ir 0.67 alloy and CB[6] that can avoid the formation of dissoluble CuIr oxides. This is the first report on using CB[6] to make binary nanoalloys, providing insights into the application of the supramolecules in functionalizing nanomaterials.
“…CB [6], which could protect alloy NPs against agglomeration and overgrowth, contributes to more uniform alloy NPs distribution in smaller sizes for different alloy compositions by steric hindrance and charge restriction. 29,32 In the inset in Figure 1b, the interplanar spacing of the CB[6]-Cu 0.33 Ir 0.67 alloy measured from the HR-TEM image is 0.21 nm, which is consistent with the lattice spacing of CuIr {111} facets. The energy dispersive X-ray spectroscopy (EDS) mapping profile (Figures 1f and 1g Next, the OER catalytic activity of all the catalysts is measured by linear sweep voltammetry (LSV) in O 2 -saturated 0.5 M H 2 SO 4 aqueous solution.…”
supporting
confidence: 63%
“…Additionally, the size measurements suggest that the series of CB[6]-Cu x Ir (1– x ) hybrids in different alloy compositions present similar sizes of ∼2.0 ± 0.3 nm (Figures S3, S4, and S5 in the Supporting Information). CB[6], which could protect alloy NPs against agglomeration and overgrowth, contributes to more uniform alloy NPs distribution in smaller sizes for different alloy compositions by steric hindrance and charge restriction. , In the inset in Figure b, the interplanar spacing of the CB[6]-Cu 0.33 Ir 0.67 alloy measured from the HR-TEM image is 0.21 nm, which is consistent with the lattice spacing of CuIr {111} facets. The energy dispersive X-ray spectroscopy (EDS) mapping profile (Figures f and g) shows that the bimetallic Cu–Ir NPs are composed of elements Cu and Ir.…”
Designing applicable high activity over long-term operation Ir-based alloy oxygen evolution reaction (OER) catalysts plays an important role in the development of the water-splitting process under acidic conditions. Herein, we report that cucurbit[6]uril-supported copper−iridium alloy (CB[6]-CuIr) hybrid with the enhancement of activity and stability for OER. The CB[6]-Cu 0.33 Ir 0.67 shows a current density of 11.68 mA/cm 2 , which is 8.4 times greater than that of Ir black at η = 280 mV. CB[6]-Cu 0.33 Ir 0.67 exhibits superior stability without activity loss after 10 h of continuous operation at 10 mA/cm 2 , while the CuIr alloy stabilized by carbon or polyvinylpyrrolidone is deactivated within 1 and 4 h, respectively. X-ray absorption fine structure (XAFS) and electron energy loss spectroscopy (EELS) confirm the interaction between the Cu 0.33 Ir 0.67 alloy and CB[6] that can avoid the formation of dissoluble CuIr oxides. This is the first report on using CB[6] to make binary nanoalloys, providing insights into the application of the supramolecules in functionalizing nanomaterials.
“…Furthermore, one-dimensional (1D) N-doped carbon nanotubes (CNTs) may provide a fast charge transfer pathway for the rapid migration of electrons-ions during the electrochemical process. [23][24][25] Also, constructing the heterostructured catalyst by interfacial electronic engineering between two or more components has been reported to be an effective strategy to enhance electrocatalytic HER activity. 26,27 Therefore, it is highly desirable to design a novel material system which can anchor a Ni 3 ZnC 0.7 /Ni heterostructure on such 1D CNTs for the improvement of catalytic HER efficiency.…”
Bimetallic carbide electrocatalysts have great potential to outperformed the well-completed single metal ones for the electrochemical hydrogen evolution reaction (HER). However, the lack of regulation tactics of electronic structures largely...
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