Department of Chemistry, Indian Institute of Technology Ropar, Rupnagar 140001, Punjab, India.
ACS Appl Mater Interfaces. 2023 Jun 14;15(23):27845-27852. doi: 10.1021/acsami.3c01318. Epub 2023 May 30.
The electrocatalytic decomposition of HS is a promising technology for H production as well as for targeting environmental pollution. But due to the lack of low-cost and efficient electrocatalysts, this technology for H production is not being explored much. Moreover, the highly toxic and copious waste HS released from industries is rarely encountered in the scientific domain. Herein, we have designed a highly efficient electrocatalyst, i.e., CoCd()S, as an anode catalyst for sulfide oxidation reaction (SOR). This optimized catalyst could drive the anode reaction at an onset potential of 0.25 V vs reversible hydrogen electrode (RHE), which was 1.27 V lower than that required for the water oxidation reaction. Moreover, we have achieved 98% H Faradaic efficiency with remarkable stability of 120 h. Thus, this method paves a path to high-value utilization of hazardous waste HS and demonstrates its great potential for hydrogen production and sulfur toward sustainable energy applications.
HS 的电化学分解是一种很有前途的制氢技术,同时也可以用于解决环境污染问题。但是,由于缺乏低成本、高效率的电催化剂,这种制氢技术还没有得到广泛的探索。此外,工业中产生的剧毒且大量的 HS 废物在科学界很少被提及。在此,我们设计了一种高效的电催化剂,即 CoCd()S,作为用于硫化物氧化反应 (SOR) 的阳极催化剂。这种优化后的催化剂可以在相对于可逆氢电极 (RHE) 为 0.25 V 的起始电势下驱动阳极反应,这比水氧化反应所需的电势低 1.27 V。此外,我们还实现了 98%的 H 法拉第效率,具有显著的 120 小时稳定性。因此,这种方法为高价值利用危险废物 HS 开辟了道路,并展示了其在可持续能源应用中制氢和硫的巨大潜力。