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Electrochemistry allows for the simultaneous conversion of hydrogen sulfide (HS) to hydrogen (H) and sulfur, achieving atomic economy, and is a sustainable and cost-effective method. At the same time, an electrolyte with high conductivity and HS absorption that can effectively capture HS in an electrochemical process is essential. An ionic liquid electrolyte system for the absorption and electrolysis of HS was constructed using the guanidine salt ionic liquid with amine-based functional groups as the carrier electrolyte, water as the solvent, and NaOH as the HS absorber. The prepared electrolyte ([TMG][IM]-AE-30) showed a strong absorption of HS with an equilibrium solubility of 100.82 g L. Under constant potential electrolysis at 1.0 V . RHE, the maximum hydrogen production rate reaches 2919.97 μmol h and the Faraday efficiency reaches 99%, and the anodic product is α-sulfur with a production of 0.881 g after electrolysis for 8 h; the current density and hydrogen production rate are still higher than those of the AE systems after three cycles. Overall, the system has good hydrogen sulfide absorption and electrolysis performances, and [TMG][IM] can effectively improve the HS absorption and electrolysis efficiencies.
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http://dx.doi.org/10.1039/d5cp01911g | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, National Center for International Research on Catalytic Technology, School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080, P. R. China.
Seawater electrolysis offers a sustainable pathway for green hydrogen production, but chloride-induced side reactions, particularly chlorine evolution (ClER), limit the stability and efficiency of catalysts. Based on an interface-engineering strategy, a bifunctional CoP-MXene electrocatalyst was designed and fabricated, in which electrons are transferred from the Ti sites of the MXene support to the adjacent Co active centers of CoP. This directional electron donation modulates the Co electronic structure, generating electron-rich Co sites that effectively suppress Cl adsorption via electronic repulsion while preserving the OH reaction pathways through favorable proton-electron coupling.
View Article and Find Full Text PDFNano Lett
September 2025
School of Electrical Engineering, Southwest Jiaotong University, Chengdu 610032, People's Republic of China.
Precise modulation of the electronic structure in transition metals, particularly the d-band center position and spin state, remains a critical challenge to expediting hydrogen evolution reaction (HER) kinetics. Herein, we report a NiPt/Ni-heterostructured catalyst enabling simultaneous optimization of the d-band electronic structure and spin state of Ni through regulation of the NiPt and Ni bridge sites. Combining operando spectroscopy, X-ray absorption spectroscopy, density functional theory, and ab initio molecular dynamics simulations, we establish that the coordination environment and spin states of Ni at the bridge sites were effectively modulated by altering the Pt content, achieving a transition of Ni centers from the low-spin to high-spin state, and optimized intermediate adsorption/desorption behaviors.
View Article and Find Full Text PDFSmall Methods
September 2025
School of Chemical Engineering, Yeungnam University, Gyeongsan, 38541, South Korea.
Constructing robust electrocatalysts and shedding light on the processes of surface reconstruction is crucial for sustained hydrogen production and a deeper understanding of catalytic behavior. Here, a novel ZIF-67-derived lanthanum- and phosphorus-co-doped CoO catalyst (La, P-CoO) has been reported. X-ray absorption spectroscopy (XAS) confirms that the La and P co-doping reduces the coordination number (CN), improves oxygen vacancies (O), and leads to lattice distortion.
View Article and Find Full Text PDFNat Chem
September 2025
Department of Interface Science, Fritz-Haber Institute of the Max Planck Society, Berlin, Germany.
The sluggish kinetics of the oxygen evolution reaction are an energetic bottleneck for green hydrogen production via water electrolysis. The reaction proceeds over a surface that undergoes (frustrated) phase transitions to accommodate bias-dependent excess charge. Here we perform Arrhenius analysis of common catalysts and correlate the activation energy and pre-exponential factor with the oxide's structural adaptation via operando X-ray absorption spectroscopy and high-energy X-ray diffraction.
View Article and Find Full Text PDFChemSusChem
September 2025
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Motooka 744, Nishi-ku, Fukuoka, 819-0395, Japan.
Engineering the local chemical environment is an emerging strategy to enhance the performance of electrochemical CO reduction reactions (CORR). Bismuth-zirconium composite catalysts (Bi-Zr-KB, where KB = Ketjen Black) are developed to leverage Zr incorporation to modulate the local CO microenvironment in an alkaline flow-cell system. Among the catalysts synthesized with various Bi/Zr ratios, the Bi-Zr-KB sample with a Bi/Zr ratio of 2 demonstrated the highest performance, achieving a current density of -176 mA cm and a formate Faradaic efficiency of 88% at -0.
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