Engineering the electronic structure of sub-nanometric Ru clusters via Pt single-atom modification for highly efficient electrocatalytic hydrogen evolution.

Developing electrocatalysts with high activity toward the hydrogen evolution reaction (HER) is a prerequisite for hydrogen fuel generation and sustainable development, but current Pt-based catalysts usually suffer from high cost and unsatisfactory performance in non-acidic media. In this work, we report an environmentally friendly and pyrolysis-free synthesis strategy to prepare an efficient catalyst, CNT-NPA-PtRu, with Pt single-atom engineered sub-nanometric Ru clusters anchored at phytic acid-modified carbon nanotubes for electrochemical HER at all pH conditions. The electronic structure of active sub-nanometric Ru clusters was optimized, which further enhanced the HER activity. The synthesized CNT-NPA-PtRu catalyst presents superior performance, reaching the current density of 10 mA cm-2 with only 18.3, 18.7 and 15 mV overpotential in alkaline, acidic and neutral electrolyte, respectively. Experimental results and theoretical calculations reveal that the single Pt atom on the sub-nanometric Ru cluster surface could modulate the electronic structure of Ru and subsequently optimize the adsorption of reaction intermediates, thus promoting HER performance. These findings underscore the importance of engineering the electronic structure of sub-nanometric clusters and offer an effective approach for the generation of high-performance electrocatalysts for HER.

Oxygen-rich ligands tailored for novel metal-organic gel electrocatalyst to promote two-electron selectivity electrocatalysis.

More extensive attention has been garnered about the H2O2 electroproduction via two-electron oxygen reduction reaction (2e- ORR). Aiming to develop a more active, more selective and more stable catalyst, herein we reported an unconventional raw metal-organic gels (MOGs) toward this process. This pioneering work, by ingeniously designing and altering the precursor ligands, achieving precisely controlling the number of oxygen groups (OGs). By elaborately comparing more than 70 samples, uncovered the significance that OGs could sufficiently promote the selectivity for H2O2 electrochemical synthesis through the two-electron pathway (realizing enhancement more than 20% in this work). The most potential Fe0.1Co0.9 MOG (H6L), performing an onset potential of 0.76 V (low overpotential), a high selectivity up to 93% ranging 0.15 V to 0.65 V (large voltage window) and 2.1 electron transfer number (implying the 2e- process dominate). This study, unlike other oxidation treatment, through the precise regulation of precursors, further confirmed the feasibility of oxygen-containing functional groups (OGs) tailoring strategy, providing a possibility for low-cost and efficient potential candidate of 2e- ORR.