Mutual Self-Regulation of d-Electrons of Single Atoms and Adjacent Nanoparticles for Bifunctional Oxygen Electrocatalysis and Rechargeable Zinc-Air Batteries
Authors: Chandrasekaran, S., Hu, R., Yao, L., Sui, L., Liu, Y., Abdelkader, A., Li, Y., Ren, X. and Deng, L.
Journal: Nano-Micro Letters
Volume: 15
Issue: 1
eISSN: 2150-5551
ISSN: 2311-6706
DOI: 10.1007/s40820-023-01022-8
Abstract:Rechargeable zinc-air batteries (ZABs) are a promising energy conversion device, which rely critically on electrocatalysts to accelerate their rate-determining reactions such as oxygen reduction (ORR) and oxygen evolution reactions (OER). Herein, we fabricate a range of bifunctional M–N–C (metal-nitrogen-carbon) catalysts containing M–N x coordination sites and M/M xC nanoparticles (M = Co, Fe, and Cu) using a new class of γ-cyclodextrin (CD) based metal–organic framework as the precursor. With the two types of active sites interacting with each other in the catalysts, the obtained Fe@C-FeNC and Co@C-CoNC display superior alkaline ORR activity in terms of low half-wave (E 1/2) potential (~ 0.917 and 0.906 V, respectively), which are higher than Cu@C-CuNC (~ 0.829 V) and the commercial Pt/C (~ 0.861 V). As a bifunctional electrocatalyst, the Co@C-CoNC exhibits the best performance, showing a bifunctional ORR/OER overpotential (ΔE) of ~ 0.732 V, which is much lower than that of Fe@C-FeNC (~ 0.831 V) and Cu@C-CuNC (~ 1.411 V), as well as most of the robust bifunctional electrocatalysts reported to date. Synchrotron X-ray absorption spectroscopy and density functional theory simulations reveal that the strong electronic correlation between metallic Co nanoparticles and the atomic Co-N4 sites in the Co@C-CoNC catalyst can increase the d-electron density near the Fermi level and thus effectively optimize the adsorption/desorption of intermediates in ORR/OER, resulting in an enhanced bifunctional electrocatalytic performance. The Co@C-CoNC-based rechargeable ZAB exhibited a maximum power density of 162.80 mW cm−2 at 270.30 mA cm−2, higher than the combination of commercial Pt/C + RuO2 (~ 158.90 mW cm−2 at 265.80 mA cm−2) catalysts. During the galvanostatic discharge at 10 mA cm−2, the ZAB delivered an almost stable discharge voltage of 1.2 V for ~ 140 h, signifying the virtue of excellent bifunctional ORR/OER electrocatalytic activity. [Figure not available: see fulltext.].
https://eprints.bournemouth.ac.uk/38320/
Source: Scopus
Mutual Self-Regulation of d-Electrons of Single Atoms and Adjacent Nanoparticles for Bifunctional Oxygen Electrocatalysis and Rechargeable Zinc-Air Batteries.
Authors: Chandrasekaran, S., Hu, R., Yao, L., Sui, L., Liu, Y., Abdelkader, A., Li, Y., Ren, X. and Deng, L.
Journal: Nanomicro Lett
Volume: 15
Issue: 1
Pages: 48
eISSN: 2150-5551
DOI: 10.1007/s40820-023-01022-8
Abstract:Rechargeable zinc-air batteries (ZABs) are a promising energy conversion device, which rely critically on electrocatalysts to accelerate their rate-determining reactions such as oxygen reduction (ORR) and oxygen evolution reactions (OER). Herein, we fabricate a range of bifunctional M-N-C (metal-nitrogen-carbon) catalysts containing M-Nx coordination sites and M/MxC nanoparticles (M = Co, Fe, and Cu) using a new class of γ-cyclodextrin (CD) based metal-organic framework as the precursor. With the two types of active sites interacting with each other in the catalysts, the obtained Fe@C-FeNC and Co@C-CoNC display superior alkaline ORR activity in terms of low half-wave (E1/2) potential (~ 0.917 and 0.906 V, respectively), which are higher than Cu@C-CuNC (~ 0.829 V) and the commercial Pt/C (~ 0.861 V). As a bifunctional electrocatalyst, the Co@C-CoNC exhibits the best performance, showing a bifunctional ORR/OER overpotential (ΔE) of ~ 0.732 V, which is much lower than that of Fe@C-FeNC (~ 0.831 V) and Cu@C-CuNC (~ 1.411 V), as well as most of the robust bifunctional electrocatalysts reported to date. Synchrotron X-ray absorption spectroscopy and density functional theory simulations reveal that the strong electronic correlation between metallic Co nanoparticles and the atomic Co-N4 sites in the Co@C-CoNC catalyst can increase the d-electron density near the Fermi level and thus effectively optimize the adsorption/desorption of intermediates in ORR/OER, resulting in an enhanced bifunctional electrocatalytic performance. The Co@C-CoNC-based rechargeable ZAB exhibited a maximum power density of 162.80 mW cm-2 at 270.30 mA cm-2, higher than the combination of commercial Pt/C + RuO2 (~ 158.90 mW cm-2 at 265.80 mA cm-2) catalysts. During the galvanostatic discharge at 10 mA cm-2, the ZAB delivered an almost stable discharge voltage of 1.2 V for ~ 140 h, signifying the virtue of excellent bifunctional ORR/OER electrocatalytic activity.
https://eprints.bournemouth.ac.uk/38320/
Source: PubMed
Mutual Self-Regulation of d-Electrons of Single Atoms and Adjacent Nanoparticles for Bifunctional Oxygen Electrocatalysis and Rechargeable Zinc-Air Batteries
Authors: Chandrasekaran, S., Hu, R., Yao, L., Sui, L., Liu, Y., Abdelkader, A., Li, Y., Ren, X. and Deng, L.
Journal: NANO-MICRO LETTERS
Volume: 15
Issue: 1
eISSN: 2150-5551
ISSN: 2311-6706
DOI: 10.1007/s40820-023-01022-8
https://eprints.bournemouth.ac.uk/38320/
Source: Web of Science (Lite)
Mutual Self-Regulation of d-Electrons of Single Atoms and Adjacent Nanoparticles for Bifunctional Oxygen Electrocatalysis and Rechargeable Zinc-Air Batteries.
Authors: Chandrasekaran, S., Hu, R., Yao, L., Sui, L., Liu, Y., Abdelkader, A., Li, Y., Ren, X. and Deng, L.
Journal: Nano-micro letters
Volume: 15
Issue: 1
Pages: 48
eISSN: 2150-5551
ISSN: 2311-6706
DOI: 10.1007/s40820-023-01022-8
Abstract:Rechargeable zinc-air batteries (ZABs) are a promising energy conversion device, which rely critically on electrocatalysts to accelerate their rate-determining reactions such as oxygen reduction (ORR) and oxygen evolution reactions (OER). Herein, we fabricate a range of bifunctional M-N-C (metal-nitrogen-carbon) catalysts containing M-Nx coordination sites and M/MxC nanoparticles (M = Co, Fe, and Cu) using a new class of γ-cyclodextrin (CD) based metal-organic framework as the precursor. With the two types of active sites interacting with each other in the catalysts, the obtained Fe@C-FeNC and Co@C-CoNC display superior alkaline ORR activity in terms of low half-wave (E1/2) potential (~ 0.917 and 0.906 V, respectively), which are higher than Cu@C-CuNC (~ 0.829 V) and the commercial Pt/C (~ 0.861 V). As a bifunctional electrocatalyst, the Co@C-CoNC exhibits the best performance, showing a bifunctional ORR/OER overpotential (ΔE) of ~ 0.732 V, which is much lower than that of Fe@C-FeNC (~ 0.831 V) and Cu@C-CuNC (~ 1.411 V), as well as most of the robust bifunctional electrocatalysts reported to date. Synchrotron X-ray absorption spectroscopy and density functional theory simulations reveal that the strong electronic correlation between metallic Co nanoparticles and the atomic Co-N4 sites in the Co@C-CoNC catalyst can increase the d-electron density near the Fermi level and thus effectively optimize the adsorption/desorption of intermediates in ORR/OER, resulting in an enhanced bifunctional electrocatalytic performance. The Co@C-CoNC-based rechargeable ZAB exhibited a maximum power density of 162.80 mW cm-2 at 270.30 mA cm-2, higher than the combination of commercial Pt/C + RuO2 (~ 158.90 mW cm-2 at 265.80 mA cm-2) catalysts. During the galvanostatic discharge at 10 mA cm-2, the ZAB delivered an almost stable discharge voltage of 1.2 V for ~ 140 h, signifying the virtue of excellent bifunctional ORR/OER electrocatalytic activity.
https://eprints.bournemouth.ac.uk/38320/
Source: Europe PubMed Central
Mutual Self-Regulation of d-Electrons of Single Atoms and Adjacent Nanoparticles for Bifunctional Oxygen Electrocatalysis and Rechargeable Zinc-Air Batteries
Authors: Chandrasekaran, S., Hu, R., Yao, L., Sui, L., Liu, Y., Abdelkader, A., Li, Y., Ren, X. and Deng, L.
Journal: Nano-Micro Letters
Volume: 15
ISSN: 2311-6706
Abstract:Rechargeable zinc-air batteries (ZABs) are a promising energy conversion device, which rely critically on electrocatalysts to accelerate their rate-determining reactions such as oxygen reduction (ORR) and oxygen evolution reactions (OER). Herein, we fabricate a range of bifunctional M–N–C (metal-nitrogen-carbon) catalysts containing M–N x coordination sites and M/M xC nanoparticles (M = Co, Fe, and Cu) using a new class of γ-cyclodextrin (CD) based metal–organic framework as the precursor. With the two types of active sites interacting with each other in the catalysts, the obtained Fe@C-FeNC and Co@C-CoNC display superior alkaline ORR activity in terms of low half-wave (E 1/2) potential (~ 0.917 and 0.906 V, respectively), which are higher than Cu@C-CuNC (~ 0.829 V) and the commercial Pt/C (~ 0.861 V). As a bifunctional electrocatalyst, the Co@C-CoNC exhibits the best performance, showing a bifunctional ORR/OER overpotential (ΔE) of ~ 0.732 V, which is much lower than that of Fe@C-FeNC (~ 0.831 V) and Cu@C-CuNC (~ 1.411 V), as well as most of the robust bifunctional electrocatalysts reported to date. Synchrotron X-ray absorption spectroscopy and density functional theory simulations reveal that the strong electronic correlation between metallic Co nanoparticles and the atomic Co-N4 sites in the Co@C-CoNC catalyst can increase the d-electron density near the Fermi level and thus effectively optimize the adsorption/desorption of intermediates in ORR/OER, resulting in an enhanced bifunctional electrocatalytic performance. The Co@C-CoNC-based rechargeable ZAB exhibited a maximum power density of 162.80 mW cm−2 at 270.30 mA cm−2, higher than the combination of commercial Pt/C + RuO2 (~ 158.90 mW cm−2 at 265.80 mA cm−2) catalysts. During the galvanostatic discharge at 10 mA cm−2, the ZAB delivered an almost stable discharge voltage of 1.2 V for ~ 140 h, signifying the virtue of excellent bifunctional ORR/OER electrocatalytic activity. [Figure not available: see fulltext.].
https://eprints.bournemouth.ac.uk/38320/
Source: BURO EPrints