ElectrochemicalLithiation Regulates the Active HydrogenSupply on Ru–Sn Nanowires for Hydrogen Evolution Toward theHigh-Performing Anion Exchange Membrane Water Electrolyzer

Designing a rational electrocatalyst/electrolyte interface with superb active hydrogen supply is of significant importance for the alkaline hydrogen evolution reaction (HER) and anion exchange membrane water electrolyzers (AEMWEs). Here, we propose a strategy to tune the interfacial active hydrogen supply via inducing dissoluble cation into electrocatalysts to boost HER in alkali, with electrochemical lithiated sub-2 nm RuSn<sub>0.8</sub> nanowires (NWs) as a proof of concept. It is found that a part of Li<sup>+</sup> could dissolve in situ from lithiated RuSn<sub>0.8</sub> NWs during HER, which tends to affect the interfacial structure and facilitate the proton transport. Among all the Li–Ru–Sn and Ru–Sn NWs, the best-performing Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs exhibit the lowest initial overpotential of 66 mV at 100 mA cm<sup>–2</sup> in 1.0 M KOH, which could be further reduced to 38 mV after the 30 000 cycles accelerated stability test (AST). In situ Raman spectroscopy and operando X-ray adsorption spectroscopy indicate that the pristine Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs are highly active toward water dissociation and the dissolved Li<sup>+</sup> during AST could further enhance the flexibility of the hydrogen bond network for proton transportation. Ab initio molecular dynamics simulations and density functional theory calculations disclose that the incorporation of Li into the Ru–Sn lattice is beneficial to lower the water dissociation barrier, while dissolved Li<sup>+</sup> at the interface significantly increases the population of interfacial water molecules, thereby providing sufficient active hydrogens for H<sub>2</sub> production. The AEMWE equipped with the Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs cathode delivers an extremely low cell voltage (1.689 V) at an industrial-scale current density (1 A cm<sup>–2</sup>) and outstanding stability (56 μV h<sup>–1</sup> loss at 1 A cm<sup>–2</sup> after 1000 h galvanostatic test), representing one of the best alkaline HER electrocatalysts ever reported.

Publication Details

Journal
Figshare
Published
2025-02-21
DOI
https://doi.org/10.1021/jacs.4c17373.s001
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

ElectrochemicalLithiation Regulates the Active HydrogenSupply on Ru–Sn Nanowires for Hydrogen Evolution Toward theHigh-Performing Anion Exchange Membrane Water Electrolyzer

Figshare
Electrocatalysts for Energy Conversion
article

ElectrochemicalLithiation Regulates the Active HydrogenSupply on Ru–Sn Nanowires for Hydrogen Evolution Toward theHigh-Performing Anion Exchange Membrane Water Electrolyzer

article en

Abstract

Designing a rational electrocatalyst/electrolyte interface with superb active hydrogen supply is of significant importance for the alkaline hydrogen evolution reaction (HER) and anion exchange membrane water electrolyzers (AEMWEs). Here, we propose a strategy to tune the interfacial active hydrogen supply via inducing dissoluble cation into electrocatalysts to boost HER in alkali, with electrochemical lithiated sub-2 nm RuSn<sub>0.8</sub> nanowires (NWs) as a proof of concept. It is found that a part of Li<sup>+</sup> could dissolve in situ from lithiated RuSn<sub>0.8</sub> NWs during HER, which tends to affect the interfacial structure and facilitate the proton transport. Among all the Li–Ru–Sn and Ru–Sn NWs, the best-performing Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs exhibit the lowest initial overpotential of 66 mV at 100 mA cm<sup>–2</sup> in 1.0 M KOH, which could be further reduced to 38 mV after the 30 000 cycles accelerated stability test (AST). In situ Raman spectroscopy and operando X-ray adsorption spectroscopy indicate that the pristine Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs are highly active toward water dissociation and the dissolved Li<sup>+</sup> during AST could further enhance the flexibility of the hydrogen bond network for proton transportation. Ab initio molecular dynamics simulations and density functional theory calculations disclose that the incorporation of Li into the Ru–Sn lattice is beneficial to lower the water dissociation barrier, while dissolved Li<sup>+</sup> at the interface significantly increases the population of interfacial water molecules, thereby providing sufficient active hydrogens for H<sub>2</sub> production. The AEMWE equipped with the Li<sub>3.0</sub>RuSn<sub>0.8</sub> NWs cathode delivers an extremely low cell voltage (1.689 V) at an industrial-scale current density (1 A cm<sup>–2</sup>) and outstanding stability (56 μV h<sup>–1</sup> loss at 1 A cm<sup>–2</sup> after 1000 h galvanostatic test), representing one of the best alkaline HER electrocatalysts ever reported.

Figshare
Clean water and sanitation
Openalex Percentile: Top 66%
Electrocatalysts for Energy Conversion
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.