International Journal of Hydrogen Energy最新文献

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Integrated CO2 capture and hydrogenation in presence of Ru–Na2ZrO3: An in-situ study
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.341
A. Sanna , K.P. Reddy , C. Emehel , G. Bagnato , I. Barba Nieto , J.W. Bos , J.A. Rodriguez
{"title":"Integrated CO2 capture and hydrogenation in presence of Ru–Na2ZrO3: An in-situ study","authors":"A. Sanna ,&nbsp;K.P. Reddy ,&nbsp;C. Emehel ,&nbsp;G. Bagnato ,&nbsp;I. Barba Nieto ,&nbsp;J.W. Bos ,&nbsp;J.A. Rodriguez","doi":"10.1016/j.ijhydene.2025.03.341","DOIUrl":"10.1016/j.ijhydene.2025.03.341","url":null,"abstract":"<div><div>Integrated CO<sub>2</sub> capture and conversion (ICCC) by hydrogenation is a promising strategy to utilize carbon dioxide and this work add to the effort to elucidate the catalytic hydrogenation mechanism using Ru based dual functional materials (DFM). Ru–Na<sub>2</sub>ZrO<sub>3</sub> DFMs, obtained through different wet methods, were evaluated for the first time and the relationship between Ru and support systematically investigated. The thermally stable and cyclable Ru–Na<sub>2</sub>ZrO<sub>3</sub>-a (obtained without filtration step) exhibited CO<sub>2</sub> conversion of 80 % and a higher yield of CO at 400 °C compared to previously tested DFM, while the Na depleted/Zr rich Ru–Na<sub>2</sub>ZrO<sub>3</sub>-b resulted in 90 % selectivity to CH<sub>4</sub> with yield of 1.11 mmol/g at the same temperature. The in-situ experiments have provided conclusive evidence showing that CO<sub>2</sub> hydrogenation on the two Ru DFMs is fundamentally different. In Ru–Na<sub>2</sub>ZrO<sub>3</sub>-a, the monoclinic Na<sub>2</sub>ZrO<sub>3</sub> support acted as the active centre (not as promoter) for CO<sub>2</sub> bridging binding and hydrogenation to CH<sub>4</sub> at the metal-support interface through associative formate pathway with limited further reduction to methane due to lack of H<sub>2</sub> spillover from the small and well dispersed Ru NPs, which results in CO desorption. Conversely, abundant clusters of larger Ru NPs in Ru–Na<sub>2</sub>ZrO<sub>3</sub>-b, led to CH<sub>4</sub> production due to co-existent Ru on-top direct dissociation of CO<sub>2</sub> (preferential) and monodentate formate adsorption and further methanation. Alkali zirconates doped metals, and their synthesis method could thus play a crucial role in designing tuneable heterogeneous catalysis in C<sub>1</sub> chemistry, which could significantly benefit the environment by lowering CO<sub>2</sub> levels, encouraging cleaner industrial practices, supporting a circular economy, and converting waste CO<sub>2</sub> into valuable products.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 118-131"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Catalysis-driven methane conversion to carbon and hydrogen
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.270
Ganesan Sivakumar , Abhijith Karattil Suresh , Debjani Nag , Pratik Swarup Dash , Ekambaram Balaraman
{"title":"Catalysis-driven methane conversion to carbon and hydrogen","authors":"Ganesan Sivakumar ,&nbsp;Abhijith Karattil Suresh ,&nbsp;Debjani Nag ,&nbsp;Pratik Swarup Dash ,&nbsp;Ekambaram Balaraman","doi":"10.1016/j.ijhydene.2025.03.270","DOIUrl":"10.1016/j.ijhydene.2025.03.270","url":null,"abstract":"<div><div>The development of catalytic materials for the efficient utilization of fundamental feedstocks into value-added products, along with hydrogen production, remains a vital and compelling area of research in the current landscape. Catalytic methane decomposition (CMD) offers a sustainable approach to carbon utilization and hydrogen production. This process transforms methane into valuable carbon-based materials, such as graphene, carbon nanotubes, and activated carbon, while concurrently generating hydrogen. This review article presents recent advancements in catalytic systems, focusing on metal-based and carbon-based catalysts for efficient methane cracking and reforming under mild conditions. It delves into the key factors affecting conversion efficiency and product selectivity, highlighting the dual benefits of simultaneous hydrogen production and carbon material synthesis. Additionally, the article addresses challenges related to catalyst stability, scalability, and economic viability, emphasizing strategies to advance sustainable methane-to-carbon conversion technologies. We strongly believe that the relatively unexplored area of methane valorization into solid carbon/carbonaceous materials with simultaneous hydrogen production holds great potential. It may pave the way for new advancements in materials science and sustainable catalysis, contributing to the design and development of innovative materials.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 42-69"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydrogen production through visible light-induced water splitting using carbon-based CoCe-MOF as novel photocatalyst
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.300
Esraa M. El-Fawal , Ahmed M.A. El Naggar
{"title":"Hydrogen production through visible light-induced water splitting using carbon-based CoCe-MOF as novel photocatalyst","authors":"Esraa M. El-Fawal ,&nbsp;Ahmed M.A. El Naggar","doi":"10.1016/j.ijhydene.2025.03.300","DOIUrl":"10.1016/j.ijhydene.2025.03.300","url":null,"abstract":"<div><div>Hydrogen as a green energy source has been increasingly emerging to decarbonize electricity production and transportation fuels, serving as a proper replacement for current fossil fuel sources. Thus, massive endeavors are done lately to develop sustainable processes for hydrogen generation. Among those methods, hydrogen production through photocatalytic aqueous reforming of methanol coupled with water splitting is considered one of the most efficient sustainable routes. In line with this methodology, the current research study introduces two novel photocatalysts (CoCe-MOF and its composite with reduced graphene oxide) for hydrogen generation from a water-methanol mixture. The textural, morphological, optical, and structural characteristics of the prepared materials were verified through various analytical techniques. Both structures revealed reasonable hydrogen productivity; however, the composite-MOF showed increased reactivity. The composition of the produced gases upon using both structures varied significantly. The explicit differences in the activities of both photocatalysts are attributed to the presence of graphene species in the composite-MOF. Statistical modeling was employed to comprehensively design the hydrogen production experiments based on preliminary experimental results that were obtained under different operating variables. A maximum hydrogen productivity of 560 mmol h<sup>−1</sup> g<sup>−1</sup>, along with a hydrogen percentage of 60 % in the produced gas, was detected for the composite-MOF under a reaction time of 1.5 h, 4 g/L as a photocatalyst dose, and a radiation power equals 3 W cm<sup>2</sup>. Both the model predictions and practical investigations were in agreement, showing that the photocatalyst dose and operating time are the most influential parameters in the hydrogen generation process. Furthermore, the recyclability of the composite photocatalyst was evaluated over six consecutive cycles under optimized conditions, confirming its increased stability. This excellent stability demonstrates the potential of the composite-MOF for long-term hydrogen production applications, reflecting the feasibility of its usage as efficient/reusable photocatalyst.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 79-95"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716237","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Porous tetra-graphene-like carbon nitride (CN) monolayer for hydrogen storage and CO2 detection
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.268
Yusuf Zuntu Abdullahi , Sohail Ahmad
{"title":"Porous tetra-graphene-like carbon nitride (CN) monolayer for hydrogen storage and CO2 detection","authors":"Yusuf Zuntu Abdullahi ,&nbsp;Sohail Ahmad","doi":"10.1016/j.ijhydene.2025.03.268","DOIUrl":"10.1016/j.ijhydene.2025.03.268","url":null,"abstract":"&lt;div&gt;&lt;div&gt;Porous two-dimensional (2D) materials have the potential to be used in many energy harvesting applications, particularly carbon capture and hydrogen (H&lt;sub&gt;2&lt;/sub&gt;) storage. This study is motivated by the successful synthesis of porous graphene with pyridinic nitrogen at the pore edges for carbon capture. To illustrate the potential of newly predicted CN, C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N, CN&lt;img&gt;Li, and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li monolayers for CO&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; capture and H&lt;sub&gt;2&lt;/sub&gt; storage, we employ first-principles density functional theory (DFT) calculations. According to the stability tests, these CN, C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N, CN&lt;img&gt;Li, and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li monolayers are mechanically, energetically, dynamically, and thermally stable. Both Perdew–Burke–Ernzerhof (PBE) and Heyd–Scuseria–Ernzerhof (HSE06) band structure results indicate that these monolayers exhibit metallic property. Additionally, we explore the performance of CN monolayer for CO&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; molecule detection. The findings suggest that moderate physiosorption characterizes the interaction between CO&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; and the CN monolayer. The CN monolayer can potentially be used as a sensing material for CO&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; molecule because of its considerable change in the work function and fast recovery time. Also, the performance of CN&lt;img&gt;Li and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li monolayers has been explore for H&lt;sub&gt;2&lt;/sub&gt; storage. It is revealed that single Li adsorption makes CN&lt;img&gt;Li and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li surfaces well-suited for considerable number of H&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; molecules uptake. Precisely, the CN&lt;img&gt;Li and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li structures can store up to 30H&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; molecules with an average E&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mi&gt;a&lt;/mi&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; values of -0.17 and -0.13 eV/H&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;, respectively. The H&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; molecule storage capacities of CN&lt;img&gt;Li@H&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt; and C&lt;span&gt;&lt;math&gt;&lt;msub&gt;&lt;mrow&gt;&lt;/mrow&gt;&lt;mrow&gt;&lt;mn&gt;2&lt;/mn&gt;&lt;/mrow&gt;&lt;/msub&gt;&lt;/math&gt;&lt;/span&gt;N&lt;img&gt;Li@H&lt;span&gt;&lt;math&gt;&lt;msub","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 150-157"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143725861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improved momentum exchange theory for a regenerative-type hydrogen recirculation blower in vehicular PEMFCs
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.324
Xu Liang, Huifang Kang, Muhammad Umar, Rui Zeng
{"title":"Improved momentum exchange theory for a regenerative-type hydrogen recirculation blower in vehicular PEMFCs","authors":"Xu Liang,&nbsp;Huifang Kang,&nbsp;Muhammad Umar,&nbsp;Rui Zeng","doi":"10.1016/j.ijhydene.2025.03.324","DOIUrl":"10.1016/j.ijhydene.2025.03.324","url":null,"abstract":"<div><div>The regenerative blowers, with their compact structure and stable performance at low flow rates, are well-suited for hydrogen recirculation in fuel cells operating under low-power conditions, particularly when paired with ejectors. However, the momentum exchange theory exhibits significant deviations when predicting the blower performance at high flow coefficients. This study investigates the limitations of the momentum exchange theory. Numerical simulations and theoretical analyses were conducted to examine the inlet/outlet area ratio (<span><math><mrow><msub><mi>A</mi><mn>1</mn></msub><mo>/</mo><msub><mi>A</mi><mn>2</mn></msub></mrow></math></span>) and velocity centroids (<span><math><mrow><msub><mi>r</mi><mn>1</mn></msub></mrow></math></span> and <span><math><mrow><msub><mi>r</mi><mn>2</mn></msub></mrow></math></span>) of the circulatory flow, and the effects of operating conditions, vane width, and flow channel width on these parameters were also studied. Two nondimensional parameters, the ratio of vane width to vane height and the ratio of flow channel width to vane height, were introduced to refine the prediction of <span><math><mrow><msub><mi>r</mi><mn>1</mn></msub></mrow></math></span> <span><math><mrow><msub><mi>r</mi><mn>2</mn></msub></mrow></math></span> and <span><math><mrow><msub><mi>A</mi><mn>1</mn></msub><mo>/</mo><msub><mi>A</mi><mn>2</mn></msub></mrow></math></span>, resulting in an improved momentum exchange theory. Validation with experimental data demonstrated enhanced prediction accuracy for flow coefficients above 0.23. Specifically, at flow coefficients of 0.424 and 0.475, the corrected model improved accuracy by 9.39 % and 13.39 %, respectively. Consequently, the overall average prediction accuracy of the corrected theory was improved. This study advances the accurate performance evaluation of similar regenerative blowers.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 132-149"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143725862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Recycling spent ternary cathodes into multi-heterogeneous Ni4N/Co5.47N/MnO composite catalysts enable efficient oxygen evolution reaction
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.303
Hongfei Jiang , Ruirui Wang , Hanhua Liu , Qianqian Liu , Miao Cheng , Wujun Ma , Jing Hu , Tao Wei , Zeda Meng , Bo Liu , Muzi Chen , Wanfei Li
{"title":"Recycling spent ternary cathodes into multi-heterogeneous Ni4N/Co5.47N/MnO composite catalysts enable efficient oxygen evolution reaction","authors":"Hongfei Jiang ,&nbsp;Ruirui Wang ,&nbsp;Hanhua Liu ,&nbsp;Qianqian Liu ,&nbsp;Miao Cheng ,&nbsp;Wujun Ma ,&nbsp;Jing Hu ,&nbsp;Tao Wei ,&nbsp;Zeda Meng ,&nbsp;Bo Liu ,&nbsp;Muzi Chen ,&nbsp;Wanfei Li","doi":"10.1016/j.ijhydene.2025.03.303","DOIUrl":"10.1016/j.ijhydene.2025.03.303","url":null,"abstract":"<div><div>Fabricating efficient electrocatalysts for water splitting through recycling ternary (LiNi<sub>1-x-y</sub>Mn<sub>x</sub>Co<sub>y</sub>O<sub>2</sub>) cathodes of spent lithium-ion batteries (LIBs) is promising and sustainable, however, the relative reasonable phase composition and microstructure still need be explored. Herein, a composite material composed of multi-heterogeneous Ni<sub>4</sub>N/Co<sub>5.47</sub>N/MnO nanoparticles coupled with porous carbon fibers was fabricated through a direct carbothermal reduction process of waste LiNi<sub>0.5</sub>Mn<sub>0.2</sub>Co<sub>0.3</sub>O<sub>2</sub> (NCM523) cathodes material dispersed into nitrogenous spinning precursor. Interestingly, this optimized material obtained at 800 °C (NCM523@CF-800) possesses abundant Ni<sub>4</sub>N/Co<sub>5.47</sub>N/MnO multi-heterostructure, endowing it with multifaceted advantages as electrocatalysts for oxygen evolution reaction (OER). Specifically, the unique structural features of multi-heterostructure promote the transfer of electrons/charges on the interface, and highly enhance the reaction kinetics. Additionally, during OER process, because of the protection of carbon matrix, Ni<sub>4</sub>N/Co<sub>5.47</sub>N/MnO has the mere surface reconstruction and forms the real active oxygen-containing species especial NiOOH. And the maintained core of Ni<sub>4</sub>N/Co<sub>5.47</sub>N/MnO provides high conductivity for the formed active oxygen-containing species. As a result, the optimized NCM523@CF-800 employed as OER electrocatalyst in water electrolysis only require 271 mV to deliver a current density of 10 mA cm<sup>−2</sup> in 1 M KOH. Meanwhile, an excellent stability of 140 h can be achieved under high current density of about 160 mA cm<sup>−2</sup>. This work may pave the way for the rapid and efficient recycling and utilization of spent battery electrode materials.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 22-30"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716165","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Metal atom-modified nickel hydroxysulfide for highly efficient electrocatalytic overall water splitting
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.302
Peng Chen , Wentao Liu , Jun Zhang , Ying Li , Runping Jia , Xiaowei Xu
{"title":"Metal atom-modified nickel hydroxysulfide for highly efficient electrocatalytic overall water splitting","authors":"Peng Chen ,&nbsp;Wentao Liu ,&nbsp;Jun Zhang ,&nbsp;Ying Li ,&nbsp;Runping Jia ,&nbsp;Xiaowei Xu","doi":"10.1016/j.ijhydene.2025.03.302","DOIUrl":"10.1016/j.ijhydene.2025.03.302","url":null,"abstract":"<div><div>The design and fabrication of high-performance, low-cost, and durable bifunctional electrocatalysts are crucial for addressing energy crises. However, significant challenges remain. In this study, we employ an oxidation-etching strategy to synthesize metal atom-modified nickel hydroxysulfide (NiSOH) (M = Fe, Cu, Co, Mn, Ce), offering advantages in simplicity, cost-effectiveness, and efficiency. Experimental results demonstrate that metal doping significantly enhances the catalytic performance of NiSOH. Notably, the bifunctional Cu–NiSOH electrode exhibits low overpotentials of 238 mV (η<sub>100</sub>) for the hydrogen evolution reaction (HER) and 289 mV (η<sub>100</sub>) for the oxygen evolution reaction (OER). Structural characterization using TEM, SEM, XRD, and XPS reveals that metal doping optimizes the microstructure, increasing the contact area between the catalyst and the electrolyte, thereby facilitating electrolyte infiltration and gas release. Additionally, DFT calculations and experimental data confirm that the incorporation of Cu atoms significantly enhances electrocatalytic activity. This work highlights the crucial role of metal atoms in improving catalytic performance and presents an effective strategy for designing metal-doped hydroxysulfides as high-performance electrocatalysts.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 14-21"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Corrigendum to “Applying artificial intelligence for forecasting behavior in a liquefied hydrogen unit” [Int J Hydrogen Energy 114 (31) (2025) 1–51]
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.255
Dongmei Jing , AzherM. Abed , Pinank Patel , D.T. Arunkumar , Damanjeet Aulakh , Bashir Salah , Ibrahim Mahariq
{"title":"Corrigendum to “Applying artificial intelligence for forecasting behavior in a liquefied hydrogen unit” [Int J Hydrogen Energy 114 (31) (2025) 1–51]","authors":"Dongmei Jing ,&nbsp;AzherM. Abed ,&nbsp;Pinank Patel ,&nbsp;D.T. Arunkumar ,&nbsp;Damanjeet Aulakh ,&nbsp;Bashir Salah ,&nbsp;Ibrahim Mahariq","doi":"10.1016/j.ijhydene.2025.03.255","DOIUrl":"10.1016/j.ijhydene.2025.03.255","url":null,"abstract":"","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"120 ","pages":"Page 601"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143715141","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Constructing Ni/Ln-CeO2 (Ln=La, Pr, Sm, Y) catalysts for low-temperature methane steam reforming (MSR): The remarkable enhancement effect of CeO2 lattice doping
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.335
Jingkang Zhong , Jiamei Ma , Yufeng Yang , Xiangyun He , Yatian Zeng , Lei Mao , Junwei Xu , Xianglan Xu , Xiuzhong Fang , Olga E. Lebedeva , Xiang Wang
{"title":"Constructing Ni/Ln-CeO2 (Ln=La, Pr, Sm, Y) catalysts for low-temperature methane steam reforming (MSR): The remarkable enhancement effect of CeO2 lattice doping","authors":"Jingkang Zhong ,&nbsp;Jiamei Ma ,&nbsp;Yufeng Yang ,&nbsp;Xiangyun He ,&nbsp;Yatian Zeng ,&nbsp;Lei Mao ,&nbsp;Junwei Xu ,&nbsp;Xianglan Xu ,&nbsp;Xiuzhong Fang ,&nbsp;Olga E. Lebedeva ,&nbsp;Xiang Wang","doi":"10.1016/j.ijhydene.2025.03.335","DOIUrl":"10.1016/j.ijhydene.2025.03.335","url":null,"abstract":"<div><div>Environmental pollution caused by fossil energy is becoming more and more stringent, and the utilization of clean energy such as H<sub>2</sub> has attracted more attention. MSR is the main way of industrial hydrogen production at present, and developing more efficient catalysts is still desirable and one of the hot issues. In this study, Ni loaded on CeO<sub>2</sub>-based solid solution supports doped by various rare earth ions (Ln = La, Pr, Sm, Y) in the matrix have been fabricated for the reaction. The reaction results have demonstrated that the catalytic performance and anti-coking ability follow the order of Ni/La<sub>1</sub>Ce<sub>19</sub> &gt; Ni/Pr<sub>1</sub>Ce<sub>19</sub> &gt; Ni/Sm<sub>1</sub>Ce<sub>19</sub> &gt; Ni/CeO<sub>2</sub> &gt; Ni/Y<sub>1</sub>Ce<sub>19</sub>. Except for Ni/Y<sub>1</sub>Ce<sub>19</sub>, the number of surface oxygen vacancies, active oxygen, basic sites and Ni active surface of the doped catalysts is improved in comparison with the unmodified Ni/CeO<sub>2</sub>. The synergistic interaction of the active oxygen anions, basic sites and the Ni active surface is the intrinsic reason to control the catalytic performance. Ni/La<sub>1</sub>Ce<sub>19</sub> owns the richest amount of both kinds of active sites and the biggest Ni surface area, thereby exhibiting the best activity, stability, coking resistance and the highest H<sub>2</sub> production rate.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 158-170"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143725858","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced stability of ammonia-fed protonic ceramic fuel cells via infiltration of Co–Fe catalyst
IF 8.1 2区 工程技术
International Journal of Hydrogen Energy Pub Date : 2025-03-28 DOI: 10.1016/j.ijhydene.2025.03.312
Haoliang Tao , Wenqiang Tang , Xueyan Zhao , Liangzhu Zhu
{"title":"Enhanced stability of ammonia-fed protonic ceramic fuel cells via infiltration of Co–Fe catalyst","authors":"Haoliang Tao ,&nbsp;Wenqiang Tang ,&nbsp;Xueyan Zhao ,&nbsp;Liangzhu Zhu","doi":"10.1016/j.ijhydene.2025.03.312","DOIUrl":"10.1016/j.ijhydene.2025.03.312","url":null,"abstract":"<div><div>In this work, Co–Fe catalysts of different molar ratios are infiltrated into protonic ceramic fuel cell (PCFC) to improve the efficiency of ammonia cracking and cell stability. The degradation rate at 600 °C decreases by as high as 88 % under a current density of 625 mA cm<sup>−2</sup>, proving the effectiveness of infiltrating Co–Fe catalysts. The postmortem analysis indicates that the infiltrated Co–Fe trends to accumulate to Ni particles in the anode and the synergism of Ni, Fe, and Co contributes to the improvement of structure integrity and cell stability in ammonia. We find that the structure evolution corresponding to cell degradation started from the regions near the anode functional layer and the separation of electrolyte grains could be regarded as the failure initiation for NH<sub>3</sub>-fed PCFC. Both electrochemical stability test and the microstructural observation suggest that a decoration of Co to Fe ratio of 1:1 is more beneficial for NH<sub>3</sub>-fed PCFC.</div></div>","PeriodicalId":337,"journal":{"name":"International Journal of Hydrogen Energy","volume":"121 ","pages":"Pages 70-78"},"PeriodicalIF":8.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143716168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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