Abstract
Consuming a substantial quantum of energy (~165 TW h), the chlor-alkali industry garners considerable scholarly and industrial interest, with the anode reaction involving the oxidation of chloride ions being a paramount determinant of reaction rates. While the dimensionally stable anode (DSA) displays commendable catalytic activity and longevity, they rely on precious metals and exhibit a non-negligible side reaction in sodium hypochlorite (NaClO) production, underscoring the appeal of metal-free alternatives. However, the molecules and systems currently available are characterized by intricate complexity and are not amenable to large-scale production. Herein, we have successfully developed an economical and highly efficient molecular catalyst, demonstrating superior performance compared with the former organic molecules in the chloride ion oxidation process (COP) for the production of both chlorine gas (Cl2) and NaClO. The molecule of 2N only needs 92 mV to reach a current density of 1000 mA cm−2, with a small cost of only 0.002 $ g−1. Furthermore, we propose a novel mechanism underpinned by non-covalent interactions, serving as the foundation for an innovative approach to the design of efficient anodes for the COP. © 2024 Wiley-VCH GmbH.
| Original language | English |
|---|---|
| Article number | e202406883 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 63 |
| Issue number | 32 |
| Online published | 24 May 2024 |
| DOIs | |
| Publication status | Published - 5 Aug 2024 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 9 Industry, Innovation, and Infrastructure
Research Keywords
- chlor-related industry
- chlorine evolution reaction
- molecule catalyst
- organo-electrocatalysis
- organocatalysts
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