首页> 外文期刊>Coordination chemistry reviews >Recent progress on metalloporphyrin-based hydrogen evolution catalysis
【24h】

Recent progress on metalloporphyrin-based hydrogen evolution catalysis

机译:基于金属卟啉的氢化催化催化的最新进展

获取原文
获取原文并翻译 | 示例
       

摘要

Designing an energy-efficient and cost-effective system for hydrogen (H-2) generation from water or proton source remains as a challenge. Precious and rare earth metals such as platinum as well as iron-dependent hydrogenase enzymes showed high activities and efficiencies for H-2 generation at low overpotential. However, Pt-based catalysts are non-affordable for large-scale applications due to limited reserves on earth and high cost. Moreover, hydrogenase enzymes have high molecular weight and relative instability under aerobic conditions. Thus, systematic strategy to design stable molecular catalysts that utilize cheap and earth-abundant transition metals with likely driving force is an attractive approach toward the H-2 economy. Accordingly, various transition metal complexes of macrocycles have been extensively reported as catalysts for H-2 generation. Metalloporphyrin macrocycles are among the most fascinating organic molecules, which have been employed in the fields of chemistry, materials science and energy relevant catalysis. Most importantly, they have been reported as potential catalysts for H-2 generation either in organic solvents or in aqueous solution. Though several porphyrin-based systems have been reported as catalysts under electrochemical or photochemical conditions over decades, there is no an inclusive review and perspective report on the application of metalloporphyrins as catalysts for H-2 production. Hence, here in we report the recent progress in potential application of metalloporphyrins as catalysts for H-2 evolution under electrochemical and photochemical conditions in aqueous solution or in organic solvents with use of organic acids as proton sources. Moreover, the methods to determine catalytic performance and mechanism of catalysis are discussed in this review. (C) 2020 Elsevier B.V. All rights reserved.
机译:为来自水或质子源产生的能量效率和成本效益的系统(H-2)产生仍然是一个挑战。珍贵和稀土金属如铂和依赖性氢酶酶,在低过电位下的H-2产生高活性和效率。然而,由于地球上的储备有限和高成本,PT基催化剂是非实惠的。此外,氢酶酶在有氧条件下具有高分子量和相对不稳定性。因此,系统策略设计利用具有可能驱动力的廉价和土木过渡金属的稳定分子催化剂是对H-2经济的有吸引力的方法。因此,宏细胞的各种过渡金属配合物已被广泛地报告为H-2代的催化剂。金属卟啉宏杂种是最迷人的有机分子中,这些有机分子是在化学,材料科学和能源相关催化领域中使用的。最重要的是,它们已被报告为在有机溶剂或水溶液中的H-2代的潜在催化剂。几十年来,虽然几种基于卟啉的系统被报告为电化学或光化学条件下的催化剂,但没有关于将金属卟啉作为H-2生产催化剂的应用的包容性审查和观点报告。因此,在我们中,我们在水溶液中的电化学和光化学条件下或在有机溶剂中报告了近期金属卟啉作为H-2演化的催化剂的催化剂的近期进展。此外,在本综述中讨论了确定催化性能和催化机制的方法。 (c)2020 Elsevier B.v.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号