Highly Durable and Efficient Seawater Electrolysis Enabled by Defective Graphene-Confined Nanoreactor.

Direct seawater electrolysis is a promising technology for massive green hydrogen production but is limited by the lack of durable and efficient electrocatalysts toward the oxygen evolution reaction (OER). Herein, we develop a core-shell nanoreactor as a high-performance OER catalyst consisting of NiFe alloys encapsulated within defective graphene layers (NiFe@DG) by a facile microwave shocking strategy. This catalyst needs overpotentials of merely 218 and 276 mV in alkalized seawater to deliver current densities of 10 and 100 mA cm-2, respectively, and operates continuously for 2000 h with negligible activity decay (1.0%), making it one of the best OER catalysts reported to date. Detailed experimental and theoretical analyses reveal that the excellent durability of NiFe@DG originates from the formation of the built-in electric field triggered by the defective graphene coating against chloride ions at the electrode/electrolyte interface, thus protecting the active NiFe alloys at the core from dissolution and aggregation under harsh operation conditions. Further, a highly stable and efficient seawater electrolyzer is assembled with the NiFe@DG anode and the Pt/C cathode to demonstrate the practicability of the catalysts.

Engineering the Morphology and Microenvironment of a Graphene-Supported Co-N-C Single-Atom Electrocatalyst for Enhanced Hydrogen Evolution.

Graphene-supported single-atom catalysts (SACs) are promising alternatives to precious metals for catalyzing the technologically important hydrogen evolution reaction (HER), but their performances are limited by the low intrinsic activity and insufficient mass transport. Herein, a highly HER-active graphene-supported Co-N-C SAC is reported with unique design features in the morphology of the substrate and the microenvironment of the single metal sites: i) the crumpled and scrolled morphology of the graphene substrate circumvents the issues encountered by stacked nanoplatelets, resulting in improved exposure of the electrode/electrolyte interfaces (≈10 times enhancement); ii) the in-plane holes in graphene preferentially orientate the Co atoms at the edge sites with low-coordinated Co-N3 configuration that exhibits enhanced intrinsic activity (≈2.6 times enhancement compared to the conventional Co-N4 moiety), as evidenced by detailed experiments and density functional theory calculations. As a result, this catalyst exhibits significantly improved HER activity with an overpotential (η) of merely 82 mV at 10 mA cm-2 , a small Tafel slope of 59.0 mV dec-1 and a turnover frequency of 0.81 s-1 at η = 100 mV, ranking it among the best Co-N-C SACs.

Electronic Structure Regulation of Single-Atom Catalysts for Electrochemical Oxygen Reduction to H2 O2.

Electrochemical synthesis of hydrogen peroxide (H2 O2 ) via the 2-electron oxygen reduction reaction (ORR) has emerged as a promising alternative to the energy-intensive anthraquinone process and catalysts combining high selectivity with superior activity are crucial for enhancing the efficiency of H2 O2 electrosynthesis. In recent years, single-atom catalysts (SACs) with the merits of maximum atom utilization efficiency, tunable electronic structure, and high mass activity have attracted extensive attention for the selective reduction of O2 to H2 O2 . Although considerable improvements are made in the performance of SACs toward the 2-electron ORR process, the principles for modulating the catalytic properties of SACs by adjusting the electronic structure remain elusive. In this review, the regulation strategies for optimizing the 2-electron ORR activity and selectivity of SACs by different methods of electronic structure tuning, including the altering of the central metal atoms, the modulation of the coordinated atoms, the substrate effect, and alloy engineering are summarized. Finally, the challenges and future prospects of advanced SACs for H2 O2 electrosynthesis via the 2-electron ORR process are proposed.

Iodine-Doping-Induced Electronic Structure Tuning of Atomic Cobalt for Enhanced Hydrogen Evolution Electrocatalysis.

The development of strategies for tuning the electronic structure of the metal sites in single-atom catalysts (SACs) is the key to optimizing their activity. Herein, we report that iodine doping within the carbon matrix of a cobalt-nitrogen-carbon (Co-N-C) catalyst can effectively modulate its electronic structure and catalytic activity toward the hydrogen evolution reaction (HER). The iodine-doped Co-N-C catalyst shows exceptional HER activity in acid with an overpotential of merely 52 mV at 10 mA cm-2, a small Tafel slope of 56.1 mV dec-1, making it among the best SACs based on both precious and nonprecious metals. Moreover, this catalyst possesses a high turnover frequency (TOF) value of 1.88 s-1 (η = 100 mV), which is about 1 order of magnitude larger than that (0.2 s-1) of the iodine-free counterpart. Experimental and theoretical studies demonstrate that the introduction of iodine dopants lowers the chemical oxidation state of the Co sites, resulting in the optimized hydrogen adsorption and facilitated HER kinetics. This work provides an alternative strategy to regulate the electronic structure of SACs for improved performance.

Design of Aligned Porous Carbon Films with Single-Atom Co-N-C Sites for High-Current-Density Hydrogen Generation.

Metal- and nitrogen-doped carbon (M-N-C) materials as a unique class of single-atom catalysts (SACs) have increasingly attracted attention as the replacement of platinum for the hydrogen evolution reaction (HER); however, their employment as HER electrodes at high current densities of industrial level remains a grand challenge. Herein, an aligned porous carbon film embedded with single-atom Co-N-C sites of exceptional activity and stability at high current densities is designed. Within the film, the atomic CoNx moieties exhibit high intrinsic activity, while the multiscale porosity of the carbon frameworks with vertically aligned microchannels afford facilitated mass transfer under the conditions of high production rate and ultrathick electrodes. Moreover, the superwetting properties of the film promote electrolyte wetting and ensure the timely removal of the evolving H2 gas bubbles. The as-designed film can work as an efficient HER electrode to deliver 500 and 1000 mA cm-2 in acid at overpotentials of 272 and 343 mV, respectively, and can operate uninterruptedly and stably at 1000 mA cm-2 for at least 32 h under static conditions. These findings pave the road toward the rational design of SACs with improved activity and stability at high current densities in gas-evolving electrocatalytic processes.