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Metal-Free Single Atom Catalyst for N2 Fixation Driven by Visible Light.

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TLDR
In this article, a metal-free photocatalyst for solar-driven nitrogen reduction was proposed by using extensive first-principles calculations, which showed that gas phase N2 can be efficiently reduced into ammonia using B/g-C3N4 through the enzymatic mechanism with a record low onset potential (0.20 V).
Abstract
Solar nitrogen (N2) fixation is the most attractive way for the sustainable production of ammonia (NH3), but the development of a highly active, long-term stable and low-cost catalyst remains a great challenge. Current research efforts for N2 reduction mainly focus on the metal-based catalysts using the electrochemical approach, while metal-free or solar-driven catalysts have been rarely explored. Herein, on the basis of a concept of electron "acceptance-donation", a metal-free photocatalyst, namely, boron (B) atom, decorated on the optically active graphitic-carbon nitride (B/g-C3N4), for the reduction of N2 is proposed by using extensive first-principles calculations. Our results reveal that gas phase N2 can be efficiently reduced into NH3 on B/g-C3N4 through the enzymatic mechanism with a record low onset potential (0.20 V). Moreover, the B-decorated g-C3N4 can significantly enhance the visible light absorption, rendering them ideal for solar-driven reduction of N2. Importantly, the as-designed catalyst is further demonstrated to hold great promise for synthesis due to its extremely high stability. Our work is the first report of metal-free single atom photocatalyst for N2 reduction, offering cost-effective opportunities for advancing sustainable NH3 production.

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Citations
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Journal ArticleDOI

Building Up a Picture of the Electrocatalytic Nitrogen Reduction Activity of Transition Metal Single-Atom Catalysts.

TL;DR: A two-step strategy is proposed for improving the eNNR activity of TM-SACs, which involves selection of the most promising family of SACs and further improvement of the activity of the best candidate in the aforementioned family via tuning the adsorption strength of the key intermediates.
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Tackling the Activity and Selectivity Challenges of Electrocatalysts toward the Nitrogen Reduction Reaction via Atomically Dispersed Biatom Catalysts

TL;DR: By means of large-scale density functional theory (DFT) computations, a descriptor-based design principle is reported to explore the large composition space of two-dimensional (2D) bi-atom catalysts (BACs) and identify three homonuclear and 28 heteronuclear BACs which could break the metal-based activity benchmark towards efficient NRR.
Journal ArticleDOI

Single-Atom Catalysts across the Periodic Table.

TL;DR: A compositional encyclopedia of SACs is provided, celebrating the 10th anniversary of the introduction of this term, and examines the coordination structures and associated properties accessed through distinct single-atom-host combinations and relate them to their main applications in thermo-, electro-, and photocatalysis.
Journal ArticleDOI

Single-boron catalysts for nitrogen reduction reaction

TL;DR: Single boron atoms supported on graphene and substituted into h-MoS2 are identified as the most promising NRR catalysts, offering excellent energy efficiency and selectivity against hydrogen evolution reaction.
Journal ArticleDOI

Highly Efficient and Selective Generation of Ammonia and Hydrogen on a Graphdiyne-Based Catalyst.

TL;DR: An atom catalyst with atomically dispersed zerovalent molybdenum atoms on graphdiyne with a high mass content of Mo atoms that was synthesized via a facile and scalable process and is the first bifunctional AC for highly efficient and selective ammonia and hydrogen generation.
References
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Journal ArticleDOI

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Atoms, molecules, solids, and surfaces: Applications of the generalized gradient approximation for exchange and correlation.

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