Electro- and Solar-Driven Fuel Synthesis with First Row Transition Metal Complexes.

Chem Rev

Christian Doppler Laboratory for Sustainable SynGas Chemistry, Department of Chemistry , University of Cambridge, Lensfield Road , Cambridge CB2 1EW , United Kingdom.

Published: February 2019

AI Article Synopsis

  • The synthesis of renewable fuels from water or CO is crucial for sustainable energy storage, with a focus on using nonprecious metal catalysts in solid-state materials.
  • The review examines 3D metal-based molecular catalysts, their immobilization on solid supports, and various applications in electro-, photo-, and photoelectrocatalytic processes for fuel synthesis in aqueous environments.
  • It discusses the efficiency and stability of these hybrid systems, while also addressing future challenges in expanding catalytic methods to produce higher-value carbon-based products beyond traditional uses.

Article Abstract

The synthesis of renewable fuels from abundant water or the greenhouse gas CO is a major step toward creating sustainable and scalable energy storage technologies. In the last few decades, much attention has focused on the development of nonprecious metal-based catalysts and, in more recent years, their integration in solid-state support materials and devices that operate in water. This review surveys the literature on 3d metal-based molecular catalysts and focuses on their immobilization on heterogeneous solid-state supports for electro-, photo-, and photoelectrocatalytic synthesis of fuels in aqueous media. The first sections highlight benchmark homogeneous systems using proton and CO reducing 3d transition metal catalysts as well as commonly employed methods for catalyst immobilization, including a discussion of supporting materials and anchoring groups. The subsequent sections elaborate on productive associations between molecular catalysts and a wide range of substrates based on carbon, quantum dots, metal oxide surfaces, and semiconductors. The molecule-material hybrid systems are organized as "dark" cathodes, colloidal photocatalysts, and photocathodes, and their figures of merit are discussed alongside system stability and catalyst integrity. The final section extends the scope of this review to prospects and challenges in targeting catalysis beyond "classical" H evolution and CO reduction to C products, by summarizing cases for higher-value products from N reduction, C products from CO utilization, and other reductive organic transformations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396143PMC
http://dx.doi.org/10.1021/acs.chemrev.8b00392DOI Listing

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