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- Publisher Website: 10.1002/aenm.202304065
- Scopus: eid_2-s2.0-85184420513
- WOS: WOS:001159110900001
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Article: Energy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling
| Title | Energy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling |
|---|---|
| Authors | |
| Keywords | Chlorine resistance Cooperative catalyst Hydrogen evolution PET waste upcycling Seawater splitting |
| Issue Date | 8-Feb-2024 |
| Publisher | Wiley |
| Citation | Advanced Energy Materials, 2024, v. 14, n. 17 How to Cite? |
| Abstract | Direct seawater electrolysis presents a promising route for grid-scale green hydrogen (H2) production without reliance on scarce freshwater. However, it is severely hampered by high energy consumption (> 4.3–5.73 kWh m−3 H2) and harmful chlorine corrosion. Herein, an energy-saving and chlorine-free H2 production system by coupling seawater splitting and upcycling of polyethylene terephthalate (PET) waste into value-added glycolic acid (GA) over a Pd─CuCo2O4 catalyst is reported. An ultra-low potential of 1.15 V versus RHE is required to achieve an industry-level current density of 600 mA cm−2, which reduces electricity cost to 2.45 kWh m−3 H2. Notably, this system maintains 1.6 A for longer than 100 h, demonstrating excellent stability. Experimental and theoretical results unveil that 1) the specific adsorption of PET-derived ethylene glycol (EG) on Pd enhances the catalytic performance, and the downshifted d-band center of Pd accelerates the desorption of GA to prevent over-oxidation; 2) the strong adsorption of OH− on CuCo2O4 synergistically promotes EG electrooxidation (EGOR) and forms a negative charge layer that effectively repels Cl− by electrostatic repulsion, thus preventing chlorine corrosion. This work may provide new opportunities for H2 production and value-added GA from vast marine resources and PET waste. |
| Persistent Identifier | http://hdl.handle.net/10722/347363 |
| ISSN | 2023 Impact Factor: 24.4 2023 SCImago Journal Rankings: 8.748 |
| ISI Accession Number ID |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Liu, Kesheng | - |
| dc.contributor.author | Gao, Xutao | - |
| dc.contributor.author | Liu, Chu Xuan | - |
| dc.contributor.author | Shi, Rui | - |
| dc.contributor.author | Tse, Edmund C.M. | - |
| dc.contributor.author | Liu, Fulai | - |
| dc.contributor.author | Chen, Yong | - |
| dc.date.accessioned | 2024-09-21T00:31:31Z | - |
| dc.date.available | 2024-09-21T00:31:31Z | - |
| dc.date.issued | 2024-02-08 | - |
| dc.identifier.citation | Advanced Energy Materials, 2024, v. 14, n. 17 | - |
| dc.identifier.issn | 1614-6832 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/347363 | - |
| dc.description.abstract | <p>Direct seawater electrolysis presents a promising route for grid-scale green hydrogen (H2) production without reliance on scarce freshwater. However, it is severely hampered by high energy consumption (> 4.3–5.73 kWh m−3 H2) and harmful chlorine corrosion. Herein, an energy-saving and chlorine-free H2 production system by coupling seawater splitting and upcycling of polyethylene terephthalate (PET) waste into value-added glycolic acid (GA) over a Pd─CuCo2O4 catalyst is reported. An ultra-low potential of 1.15 V versus RHE is required to achieve an industry-level current density of 600 mA cm−2, which reduces electricity cost to 2.45 kWh m−3 H2. Notably, this system maintains 1.6 A for longer than 100 h, demonstrating excellent stability. Experimental and theoretical results unveil that 1) the specific adsorption of PET-derived ethylene glycol (EG) on Pd enhances the catalytic performance, and the downshifted d-band center of Pd accelerates the desorption of GA to prevent over-oxidation; 2) the strong adsorption of OH− on CuCo2O4 synergistically promotes EG electrooxidation (EGOR) and forms a negative charge layer that effectively repels Cl− by electrostatic repulsion, thus preventing chlorine corrosion. This work may provide new opportunities for H2 production and value-added GA from vast marine resources and PET waste.</p> | - |
| dc.language | eng | - |
| dc.publisher | Wiley | - |
| dc.relation.ispartof | Advanced Energy Materials | - |
| dc.subject | Chlorine resistance | - |
| dc.subject | Cooperative catalyst | - |
| dc.subject | Hydrogen evolution | - |
| dc.subject | PET waste upcycling | - |
| dc.subject | Seawater splitting | - |
| dc.title | Energy-Saving Hydrogen Production by Seawater Splitting Coupled with PET Plastic Upcycling | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1002/aenm.202304065 | - |
| dc.identifier.scopus | eid_2-s2.0-85184420513 | - |
| dc.identifier.volume | 14 | - |
| dc.identifier.issue | 17 | - |
| dc.identifier.eissn | 1614-6840 | - |
| dc.identifier.isi | WOS:001159110900001 | - |
| dc.identifier.issnl | 1614-6832 | - |
