Reductive Supramolecular In Situ Construction of Nano‐Platinum Effectively Couples Cathodic Hydrogen Evolution and Anodic Alcohol Oxidation DOI Creative Commons
Rui Bai,

Qiao Ye,

Cuiyu Li

и другие.

Advanced Science, Год журнала: 2025, Номер unknown

Опубликована: Апрель 3, 2025

The deployment of high-performance catalysts and the acceleration anodic reaction kinetics are key measures to achieve maximum energy efficiency in overall water electrolysis hydrogen production systems. Here, an innovative strategy is developed by directly constructing a supramolecular framework embedded with boron clusters cucurbituril as reducing agent. This approach enabled situ conversion Pt⁴⁺ into highly dispersed, small-sized nano-platinum, which subsequently distributed on boron-carbon-nitrogen (BCN) matrix. resulting Pt/BNHCSs catalyst demonstrates ability facilitate electrocatalytic splitting for across multiple scenarios while simultaneously accelerating methanol oxidation kinetics, significantly outperforming commercial Pt/C various aspects. cathodic evolution-anodic coupling system constructed using greatly reduces consumption system. In attenuated total reflection Fourier transform infrared online differential electrochemical mass spectrometry reveals that interface enhances H₂O adsorption promotes CH₃OH→CO process, density functional theory calculations indicated BCN support facilitated evolution H₂ CH₃OH CO, elucidating mechanism promoted oxidation.

Язык: Английский

Hard Lewis acid induced chloride repulsion for durable neutral seawater electrolysis DOI

Suyang Feng,

Gai Li, Qingyi Wei

и другие.

Nano Energy, Год журнала: 2025, Номер unknown, С. 110714 - 110714

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Research progress of Ce-based electrocatalysts in hydrogen evolution reaction DOI
D. Cao,

Meiwen Tie,

Guangrui Zhang

и другие.

Journal of Rare Earths, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

Stabilizing Bulk Lattice Oxygen Via the Enhancement of Ir/Ru–O Bonds for Stable Oxidation Catalysts in Acidic Media DOI
Han Wang,

xiaohua chen,

Yubin Chen

и другие.

Опубликована: Янв. 1, 2025

Язык: Английский

Процитировано

0

High-entropy heterostructure electrocatalyst with built-in electric field regulation for efficient oxygen evolution reaction DOI

Xuehao Li,

Peng Wang, Mang Niu

и другие.

Applied Surface Science, Год журнала: 2025, Номер unknown, С. 162626 - 162626

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Advances in the Energy‐Saving Electro‐Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Furandicarboxylic Acid DOI Open Access

Yujie Ren,

Shilin Fan,

Yu Xiao

и другие.

Advanced Sustainable Systems, Год журнала: 2025, Номер unknown

Опубликована: Фев. 5, 2025

Abstract As a pivotal bio‐based building block, 2,5‐furandicarboxylic acid (FDCA) holds immense and broad application potential in the chemistry industry. Its polymeric derivative, polyethylene furandicarboxylate (PEF), emerges as an appealing alternative to conventional petroleum‐based terephthalate (PET). The electrochemical route for oxidizing 5‐hydroxymethylfurfural (HMF) into FDCA presents significant advantages over thermochemical processes, without requirements of high temperature, pressure, chemical oxidants, precious metal catalysts, featuring higher energy efficiency. Furthermore, electrosynthesis at anode can be synergistically integrated with selective reduction reactions cathode, enabling simultaneous production two desirable value‐added products further enhancing overall utilization This work reviews advancements electrocatalytic HMF (EHTF), encompassing catalyst design, reaction mechanisms, coupling strategies, reactor configurations. It also indicates challenges opportunities EHTF provides insights future development directions.

Язык: Английский

Процитировано

0

Balancing the competitive adsorption of urea and OH− over V-NiCo@NC for enhancing urea electrolysis at high current density DOI

Zhixiang Zhai,

Miaojing Pan,

Jia Wu

и другие.

Chemical Engineering Journal, Год журнала: 2025, Номер unknown, С. 160565 - 160565

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Valorization of Organic Wastes as Carbon Sources for Electrode Manufacturing in Hydrogen Production: A Critical Review DOI
E. López-Fernández,

J. Comendador,

Á. Ramírez-Vidal

и другие.

Electrochimica Acta, Год журнала: 2025, Номер unknown, С. 145872 - 145872

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Defect-Rich Co(OH)2 Induced by Carbon Dots for Oxygen Evolution Reaction DOI Open Access
Xuan Han,

Chao Guo,

Hui Wang

и другие.

Catalysts, Год журнала: 2025, Номер 15(3), С. 219 - 219

Опубликована: Фев. 26, 2025

Hydrogen production from water electrolysis offers a highly promising and sustainable route to solve the energy crisis. However, it is severely limited by sluggish kinetics of oxygen evolution reaction (OER) occurring on anode. Herein, employing carbon dots functionalized with benzene sulfonate groups (BS-CDs) as distinctive inductor, Co(OH)2 catalyst featuring abundant defects was synthesized for an enhanced OER. The hydrophilic nature BS-CDs exerts significant interfacial induction effect growth dynamics Co(OH)2, fostering formation elevated crystal substantial quantity vacancies. resulting BS-CDs/Co(OH)2 requires overpotential only 340 mV achieve current density 10 mA cm−2 in alkaline media, demonstrating markedly improved OER activity compared pristine N-CDs/Co(OH)2 induced amine-modified CDs. Furthermore, structural integrity maintained, retention rate 92% observed following 20 h stability assessment. This work provides novel approach developing cost-effective transition metal catalysts that exhibit exceptional catalytic efficiency excellent

Язык: Английский

Процитировано

0

Bifunctional transition-metal catalysts for energy-saving hydrogen generation from nitrogenous wastewater DOI
Yue Zhou, Liang Zhang, Xin Yang

и другие.

Chemical Communications, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

Wastewater from industrial chemical synthesis, agricultural activities, and domestic sewage usually contains high levels of nitrogenous compounds, endangering environmental health human well-being. Nitrogenous wastewater electrolysis (NWE), despite its ecological merits, is inherently hampered by sluggish kinetics. To improve process efficiency, lower costs, avoid cross-contamination between the anode cathode, a range bifunctional transition-metal catalysts capable efficient operation at both electrodes have recently been developed. This review outlines progress in these for energy-saving production hydrogen wastewater, including urea, hydrazine, ammonia. It highlights their dual role degrading pollutants generating energy. The meticulously introduces key performance metrics NWE system surveys latest advancements catalysts, along with catalytic mechanisms. culminates detailed summary comparative analysis representative emphasizing electricity consumption efficiency. Lastly, existing challenges research prospects are thoroughly discussed.

Язык: Английский

Процитировано

0

Electrochemical N–N Oxidatively Coupled Dehydrogenation of 3,5-Diamino-1H-1,2,4-triazole for Value-Added Chemicals and Bipolar Hydrogen Production DOI Creative Commons
Jiachen Li, Yang Li,

Yuqiang Ma

и другие.

Journal of the American Chemical Society, Год журнала: 2025, Номер unknown

Опубликована: Март 8, 2025

Electrochemical H2 production from water favors low-voltage molecular oxidation to replace the oxygen evolution reaction as an energy-saving and value-added approach. However, there exists a mismatch between high demand for slow anodic reactions, restricting practical applications of such hybrid systems. Here, we propose bipolar approach, with generation N–N oxidatively coupled dehydrogenation (OCD) 3,5-diamino-1H-1,2,4-triazole (DAT), in addition cathodic generation. The system requires relatively low potentials 0.872 1.108 V vs RHE reach 10 500 mA cm–2, respectively. H-type electrolyzer only 0.946 1.129 deliver 100 respectively, electricity consumption (1.3 kWh per m3 H2) reduced by 68%, compared conventional splitting. Moreover, process is highly appealing due absence traditional hazardous synthetic conditions azo compounds at anode crossover/mixing H2/O2 electrolyzer. A flow-type operates stably cm–2 300 h. Mechanistic studies reveal that Pt single atom nanoparticle (Pt1,n) optimize adsorption S active sites over Pt1,n@VS2 catalysts. At anode, stepwise −NH2 DAT then oxidative coupling −N–N– predominantly form while generating H2. present report paves new way atom-economical aminotriazole green electrosynthesis chemicals.

Язык: Английский

Процитировано

0