Abstract:SiO2 and γ‐Al2O3 impregnation with nominal 10 and 20% of cobalt was examined using wet impregnation method starting with Co(NO3)2·6H2O. The samples were dried and analyzed by XPS prior to calcination to study the surface species in the solids and the role of the support in the processing of supported cobalt catalysts. The results showed that cobalt introduction alters the few top nanometers of the support materials as there are significant changes recorded in the XPS spectra. Most importantly, there is a remar… Show more
“…The spectrum showed two distinct peaks at 75.3 and 72.3 eV corresponding to the Al 2p core level of Al-O and Li-Al-O bonds on the surface, respectively. [49,50] These results confirm the high uniformity of the Zr/Y doping and Al 2 O 3 coating in Zr 25 Y 15 -NCM@Al 20 , without a large population of agglomerates for any of the five elements. Furthermore, the analysis by inductively coupled plasma atomic emission spectroscopy (ICP-AES) shows that the measured values were well matched with the target composition of the samples (Table S1, Supporting Information).…”
High Ni-layered oxides are promising cathode candidates for lithium-ion batteries (LIBs) owing to their high-specific capacity, high energy density, and low cost. However, their thermal and cycling performances often suffer from the inevitable interfacial reactions, oxygen loss, transition metal dissolution, and irreversible H2-H3 lattice distortion. Herein, small doses of Zr/Y codoped and Al 2 O 3 coated single-crystal high-Ni NCM (LiNi 0.83 Co 0.12 Mn 0.05 O 2 ) materials (ZrY-NCM@Al) are synthesized via a facile high-temperature solidstate reaction. The Al 2 O 3 surface coating works as a protective layer to inhibit the side reaction on the interface between electrodes and electrolytes. The Zr/Y co-doping improves the structural stability of the NCM and suppresses the irreversible structure transition from H2 to H3. When ZrY-NCM@Al is used as a cathode, the square-aluminum-shell full battery with artificial graphite anode exhibits a high capacity of 50 Ah and a high energy density of 230 Wh kg −1 . After 1000 cycles at 45 °C and 1 C constant current and constant voltage (CCCV), the battery retained 89.2% of its capacity and an energy density of 204 Wh kg −1 , demonstrating excellent thermal and cycling performances. This study paves a novel route to the fabrication of high-Ni cathode materials for LIBs with excellent cycling and thermal stability.
“…The spectrum showed two distinct peaks at 75.3 and 72.3 eV corresponding to the Al 2p core level of Al-O and Li-Al-O bonds on the surface, respectively. [49,50] These results confirm the high uniformity of the Zr/Y doping and Al 2 O 3 coating in Zr 25 Y 15 -NCM@Al 20 , without a large population of agglomerates for any of the five elements. Furthermore, the analysis by inductively coupled plasma atomic emission spectroscopy (ICP-AES) shows that the measured values were well matched with the target composition of the samples (Table S1, Supporting Information).…”
High Ni-layered oxides are promising cathode candidates for lithium-ion batteries (LIBs) owing to their high-specific capacity, high energy density, and low cost. However, their thermal and cycling performances often suffer from the inevitable interfacial reactions, oxygen loss, transition metal dissolution, and irreversible H2-H3 lattice distortion. Herein, small doses of Zr/Y codoped and Al 2 O 3 coated single-crystal high-Ni NCM (LiNi 0.83 Co 0.12 Mn 0.05 O 2 ) materials (ZrY-NCM@Al) are synthesized via a facile high-temperature solidstate reaction. The Al 2 O 3 surface coating works as a protective layer to inhibit the side reaction on the interface between electrodes and electrolytes. The Zr/Y co-doping improves the structural stability of the NCM and suppresses the irreversible structure transition from H2 to H3. When ZrY-NCM@Al is used as a cathode, the square-aluminum-shell full battery with artificial graphite anode exhibits a high capacity of 50 Ah and a high energy density of 230 Wh kg −1 . After 1000 cycles at 45 °C and 1 C constant current and constant voltage (CCCV), the battery retained 89.2% of its capacity and an energy density of 204 Wh kg −1 , demonstrating excellent thermal and cycling performances. This study paves a novel route to the fabrication of high-Ni cathode materials for LIBs with excellent cycling and thermal stability.
“…2f shows the presence of O, the combination of the three fitted peaks at 530.5, 531.2, and 531.6 eV, which can be attributed to the typical bands of metal hydroxyl (M–OH), carbonate (CO 3 ), and C–OH bonds, respectively. 59 The electrode morphologies were examined by SEM. The nanostructures of the binary and ternary electrodes were uniformly grown on a Ni foam substrate, as shown in Fig.…”
“…In Figure 4e, the spectrum of Al 2p was fitted into one sub‐peak, Al 3+ 2p at 75.23 eV. [ 49 ] The Al element in Al 2 O 3 , AlCl 3 , KAlCl 4 , and K 3 AlCl 6 were all present as Al 3+ . The Sn 3d spectrum in Figure 4f was fitted into four sub‐peaks, Sn3d 5/2 at 484.65 eV and Sn3d 3/2 at 493.12 eV, Sn 4+ 3d 5/2 at 487.43 eV and Sn 4+ 3d 3/2 at 495.90 eV.…”
The further applications of liquid metals (LMs) are limited by their common shortcoming of silver‐white physical appearance, which deviates from the impose stringent requirements for color and aesthetics. Herein, a concept is proposed for constructing fluorescent core–shell structures based on the components and properties of LMs, and metal halides. The metal halides endow LMs with polychromatic and stable fluorescence characteristics. As a proof‐of‐concept, LMs‐Al obtained by mixing of LMs with aluminum (Al) is reported. The surface of LMs‐Al is transformed directly from Al to a multi‐phase metal halide of K3AlCl6 with double perovskites structure, via redox reactions with KCl + HCl solution in a natural environment. The formation of core–shell structure from the K3AlCl6 and LMs is achieved, and the shell with different phases can emit a cyan light by the superimposition of the polychromatic spectrum. Furthermore, the LMs can be directly converted into a fluorescent shell without affecting their original features. In particular, the luminescence properties of shells can be regulated by the components in LMs. This study provides a new direction for research in spontaneous interfacial modification and fluorescent functionalization of LMs and promises potential applications, such as lighting and displays, anti‐counterfeiting measures, sensing, and chameleon robots.
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