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A review on the recent advances in the design and structure–activity relationship of TiO2-based photocatalysts for solar hydrogen production 基于 TiO2 的太阳能制氢光催化剂的设计和结构-活性关系的最新进展综述
IF 3.2
Energy advances Pub Date : 2024-06-10 DOI: 10.1039/D4YA00249K
Sunesh S. Mani, Sivaraj Rajendran, Thomas Mathew and Chinnakonda S. Gopinath
{"title":"A review on the recent advances in the design and structure–activity relationship of TiO2-based photocatalysts for solar hydrogen production","authors":"Sunesh S. Mani, Sivaraj Rajendran, Thomas Mathew and Chinnakonda S. Gopinath","doi":"10.1039/D4YA00249K","DOIUrl":"10.1039/D4YA00249K","url":null,"abstract":"<p >The major issues that determine the efficiency of photocatalyst composite materials for solar hydrogen production, with or without a sacrificial agent, are efficient visible light harvesting properties, efficient separation of charge carriers and their utilization of redox sites, and stability. Thus, significant efforts have been devoted in the past few decades to modify the above characteristics by integrating constituent components of composites using different approaches. In the present review, we aim to summarize the recent advances, predominantly, in the area of TiO<small><sub>2</sub></small>-based photocatalyst composites for solar hydrogen production. Firstly, we present the recent progress in material integration aspects by discussing the integration of TiO<small><sub>2</sub></small> with different categories of materials, including noble/3d metals, metal oxides/sulphides/selenides, other low bandgap semiconductors, C-based materials, and dye sensitizers. Furthermore, we discuss how material integration helps in tailoring the electronic and optical properties for activity tuning in solar H<small><sub>2</sub></small> production. Subsequently, critical changes in the physico-chemical and electronic properties of composites with respect to their preparation methods, morphology, crystallographic facets, particle size, dopant, calcination temperature, and structure–activity relationship to solar hydrogen production are addressed in detail. Moreover, we discuss the importance of fabricating a photocatalyst in a thin film form and performing solar hydrogen production in different reactor set-ups for enhancing its photocatalytic performance, while addressing device scalability. Despite the significant advancements made in this field, solar-to-hydrogen conversion efficiency still needs to be improved to realise the practical application of solar hydrogen production. In this case, the direct conversion of water to hydrogen <em>via</em> overall water splitting and renewable H<small><sub>2</sub></small> production from wastewater or biomass components by employing suitable photocatalysts are some possible ways to improve the energy efficiency, and continuous research in the above directions is highly desirable.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00249k?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141507495","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Teaching an old dog new tricks: Ti-doped ZnFe2O4 as active material in zinc ion batteries – a proof of concept† 教老狗学新招:作为锌离子电池活性材料的掺钛锌铁氧体--概念验证
IF 3.2
Energy advances Pub Date : 2024-06-10 DOI: 10.1039/D4YA00134F
S. Krämer, J. Hopster, A. Windmüller, R.-A. Eichel, M. Grünebaum, T. Jüstel, M. Winter and K. Neuhaus
{"title":"Teaching an old dog new tricks: Ti-doped ZnFe2O4 as active material in zinc ion batteries – a proof of concept†","authors":"S. Krämer, J. Hopster, A. Windmüller, R.-A. Eichel, M. Grünebaum, T. Jüstel, M. Winter and K. Neuhaus","doi":"10.1039/D4YA00134F","DOIUrl":"10.1039/D4YA00134F","url":null,"abstract":"<p >In this work, the suitability of the spinel material ZnFe<small><sub>2</sub></small>O<small><sub>4</sub></small>, which has already been widely investigated in the context of its magnetic and photocatalytic properties, for use as active material for the cathode side in zinc ion batteries is presented. In addition to pure ZnFe<small><sub>2</sub></small>O<small><sub>4</sub></small>, part of the Fe<small><sup>3+</sup></small> was doped with Ti<small><sup>4+</sup></small> to achieve stabilization of Zn vacancies in the material and increase ionic conductivity as indicated by previous modelling results. Ceramic samples with the composition ZnFe<small><sub>2−<em>x</em></sub></small>Ti<small><sub><em>x</em></sub></small>O<small><sub>4</sub></small> (<em>x</em> = 0 to 0.25) were prepared <em>via</em> a Pechini synthesis route and investigated regarding their optical, structural and electrochemical characteristics. It has been successfully demonstrated that both pure and Ti doped ZnFe<small><sub>2</sub></small>O<small><sub>4</sub></small> can be used as active material in the positive electrodes of zinc metal batteries or in an “anode-free” setup with Sn metal. Cells with calcined ZnFe<small><sub>2<em>x</em></sub></small>Ti<small><sub><em>x</em></sub></small>O<small><sub>4</sub></small> (<em>x</em> = 0.09)|0.5 M zinc triflate in acetonitrile|Zn showed a stable cycling behavior over 1000 cycles and an average initial specific capacity of 55 mA h g<small><sup>−1</sup></small>.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00134f?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141512419","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
On the effect of gas generation on heat transfer during thermal runaway of pouch cells 袋式电池热失控过程中气体生成对传热的影响
IF 3.2
Energy advances Pub Date : 2024-06-07 DOI: 10.1039/D4YA00205A
Niklas Weber, Sebastian Schuhmann, Robert Löwe, Jens Tübke and Hermann Nirschl
{"title":"On the effect of gas generation on heat transfer during thermal runaway of pouch cells","authors":"Niklas Weber, Sebastian Schuhmann, Robert Löwe, Jens Tübke and Hermann Nirschl","doi":"10.1039/D4YA00205A","DOIUrl":"10.1039/D4YA00205A","url":null,"abstract":"<p >Lithium-ion batteries produce a vast amount of gases during decomposition reactions and thermal runaway. While the amount and composition of these gases has been investigated in the past, little is known about their impact on thermal transport inside the battery cell. Especially for pouch cells, which do not have a rigid housing, this becomes even more important in multi-cell scenarios since thermal propagation is governed by heat transfer. In this work, a simulation framework is presented that enhances the chemical single cell model by accounting for these thermal transport changes in gas producing pouch cells. It is validated by performing two battery cell propagation experiments in an autoclave. Besides the temperature measurement, the propagation time between the cells and the gas composition are analyzed and compared between simulation and experiment. Further, it is investigated how the application of an external pressing force impacts the heat transfer and thus the propagation behavior. In the given setup, the propagation time decreased from 37.2 s to 16.8 s with increasing pressing force.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00205a?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141512423","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bioinspired flavin analogues as organic electrode materials for supercapacitor applications† 生物启发黄素类似物作为超级电容器应用的有机电极材料
IF 3.2
Energy advances Pub Date : 2024-06-05 DOI: 10.1039/D4YA00001C
Dipayan Mondal, Ishita Naskar, Melepurath Deepa and Ashutosh Kumar Mishra
{"title":"Bioinspired flavin analogues as organic electrode materials for supercapacitor applications†","authors":"Dipayan Mondal, Ishita Naskar, Melepurath Deepa and Ashutosh Kumar Mishra","doi":"10.1039/D4YA00001C","DOIUrl":"10.1039/D4YA00001C","url":null,"abstract":"<p >With the increasing interest in incorporating redox-active organic molecules as potential materials in energy storage systems, we envisaged a chemical design of a naturally occurring redox-active flavin moiety. Herein, we report the fabrication and characterization of asymmetric supercapacitors (ASCs) based on modified flavins as cathode materials. Notably, subtle chemical modification with the incorporation of a carboxylic functionality around the flavin core (<strong><em>c</em>Fl</strong>) was found to impart superior ion-storage properties compared to a simple flavin derivative (<strong>Fl</strong>). As determined, the specific capacitance (SC) for <strong><em>c</em>Fl</strong> and <strong>Fl</strong> as individual electrodes was found to be 170 and 62 F g<small><sup>−1</sup></small>, respectively, whereas in a two electrode ASC with activated carbon serving as the anode, the SC was found to be 107 and 29 F g<small><sup>−1</sup></small>, respectively, at a current density of 1.25 A g<small><sup>−1</sup></small>. With better cycling stability (retaining 87% of its initial SC in the case of <strong><em>c</em>Fl</strong>) and significantly higher energy density (38 W h kg<small><sup>−1</sup></small> for <strong><em>c</em>Fl</strong>) as compared to most of the known organic material-based electrodes, the modified flavin derivatives serve as better organic electrode alternatives for practical energy storage applications.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00001c?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141254001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Alkylation of α-pinene with isobutene/isobutane over Hβ zeolite† 在 Hβ 沸石上用异丁烯/异丁烷烷基化 α-蒎烯
IF 3.2
Energy advances Pub Date : 2024-06-04 DOI: 10.1039/D4YA00291A
Zhaocai Jiao, Mingzu Liu, Ningbo Yang, Fengli Yu, Congxia Xie, Shitao Yu and Bing Yuan
{"title":"Alkylation of α-pinene with isobutene/isobutane over Hβ zeolite†","authors":"Zhaocai Jiao, Mingzu Liu, Ningbo Yang, Fengli Yu, Congxia Xie, Shitao Yu and Bing Yuan","doi":"10.1039/D4YA00291A","DOIUrl":"10.1039/D4YA00291A","url":null,"abstract":"<p >α-Pinene and isobutene/isobutane can undergo hybrid alkylation under acid catalysis, resulting in C<small><sub>14</sub></small> and C<small><sub>20</sub></small> product fractions with favorable bio-based high-energy-density fuel properties after hydrogenation. In this study, the catalytic performance of zeolite molecular sieves, such as Hβ, HY, HZSM-5, HZSM-35, HSAPO-11, was investigated for the alkylation of α-pinene and Isobut-5 (a mixture of isobutene/isobutane with a mass ratio of 1 : 5) given the acidic sites and specific pore structures with shape-selective abilities of zeolite catalysts. Various characterization techniques, including temperature-programmed desorption of ammonia (NH<small><sub>3</sub></small>-TPD), Fourier transform infrared spectroscopy with pyridine adsorption (Py-IR), N<small><sub>2</sub></small> adsorption/desorption, X-ray fluorescence spectrum (XRF), and particle size analysis, were conducted to analyze the acidic properties, pore characteristics, silica–aluminum ratio, and grain size of the zeolites, and their influence on the alkylation of α-pinene and Isobut-5. Moreover, the recycling performance of the favorite Hβ-25n catalyst and an effective regeneration method were investigated using temperature-programmed oxidation (TPO) analysis. This study provides essential research data for the preparation of α-pinene-based high-energy-density fuels.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00291a?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141254239","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of binderless LTA and SAPO-34 beads as CO2 adsorbents for biogas upgrading in a vacuum pressure swing adsorption setup† 在真空变压吸附装置中将无粘合剂 LTA 和 SAPO-34 珠子作为二氧化碳吸附剂用于沼气升级的评估
IF 3.2
Energy advances Pub Date : 2024-05-31 DOI: 10.1039/D4YA00007B
Dina G. Boer, Henk H. van de Bovenkamp, Jort Langerak, Benny Bakker and Paolo P. Pescarmona
{"title":"Evaluation of binderless LTA and SAPO-34 beads as CO2 adsorbents for biogas upgrading in a vacuum pressure swing adsorption setup†","authors":"Dina G. Boer, Henk H. van de Bovenkamp, Jort Langerak, Benny Bakker and Paolo P. Pescarmona","doi":"10.1039/D4YA00007B","DOIUrl":"10.1039/D4YA00007B","url":null,"abstract":"<p >Biogas upgrading by selective adsorption of CO<small><sub>2</sub></small> using vacuum pressure swing adsorption (VPSA) is a technology that can enable the utilization of the isolated biomethane as a direct replacement for natural gas. In this work, we report for the first time the investigation of LTA and SAPO-34 macroscopic beads with hierarchical porosity as CO<small><sub>2</sub></small> adsorbents in a VPSA setup. While a binder is generally required to shape zeolites and zeotypes into the macroscopic format (<em>e.g.</em> beads, pellets) needed for application in a VPSA column, in this work binderless LTA and SAPO-34 beads were studied and compared with commercial binder-containing zeolite 4A beads. Binary breakthrough experiments were conducted with a gas mixture mimicking biogas (<em>i.e.</em> 40 vol% CO<small><sub>2</sub></small> and 60 vol% CH<small><sub>4</sub></small>) in a single adsorption column up to 4 bar. The SAPO-34 beads displayed a slightly steeper breakthrough with less significant tailing compared to the LTA beads, which was ascribed to faster intra-crystalline diffusion due to the different framework structure and the lower adsorption strength of CO<small><sub>2</sub></small> on SAPO-34 compared to LTA. Notably, both the binderless LTA and SAPO-34 beads displayed a slightly sharper breakthrough and less significant tailing compared to commercial 4A beads. This was attributed to the open and accessible hierarchical pore structure of the binderless beads. The CO<small><sub>2</sub></small> adsorption capacity for the SAPO-34 beads was relatively stable over 5 cycles, while the LTA and commercial 4A beads displayed a significant decrease in adsorption capacity from the first to the second cycle. For the SAPO-34 beads, a cyclic adsorption capacity at breakthrough around 2 mmol g<small><sup>−1</sup></small> and a CO<small><sub>2</sub></small> productivity &gt; 3 mol kg<small><sup>−1</sup></small> h<small><sup>−1</sup></small> were achieved. These values are significantly higher than those of the LTA and commercial 4A beads, making the SAPO-34 beads a promising candidate for industrial application in VPSA.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00007b?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141196951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The effect of oxygen on NiO as a back buffer layer in CdTe solar cells 氧对碲化镉太阳能电池中作为背缓冲层的氧化镍的影响
IF 3.2
Energy advances Pub Date : 2024-05-30 DOI: 10.1039/D4YA00125G
Nicholas Hunwick, Xiaolei Liu, Mustafa Togay, John M. Walls, Jake Bowers and Patrick J. M. Isherwood
{"title":"The effect of oxygen on NiO as a back buffer layer in CdTe solar cells","authors":"Nicholas Hunwick, Xiaolei Liu, Mustafa Togay, John M. Walls, Jake Bowers and Patrick J. M. Isherwood","doi":"10.1039/D4YA00125G","DOIUrl":"10.1039/D4YA00125G","url":null,"abstract":"<p >Thin film CdTe-based photovoltaic devices have achieved high efficiency above 22%. However, the device performance is limited by large open circuit voltage deficit. One of the primary reasons is non-ohmic back contacts. In this work, nickel oxide is used as a back buffer layer to form an ohmic back contact. We comprehensively investigate oxygen effects during sputtering on film properties and device performance. Increased oxygen in the deposition environment led to darker films, increased carrier concentration, decreased mobility and decreased resistivity. X-ray photoelectron spectroscopy showed peak shifts favouring Ni<small><sup>3+</sup></small> over Ni<small><sup>2+</sup></small>, and X-ray diffraction demonstrated that crystallinity hit a peak at around 5% oxygen input. The NiO back buffer layer improves device performance by reducing barrier height at the gold back contact and improving valence band offset at the CdTe/NiO interface. The NiO layer deposited without oxygen improved the <em>V</em><small><sub>oc</sub></small> to 710 mV, from a baseline of 585 mV. At 5% and 20% oxygen content during deposition, efficiency improved relative to the reference due to an increase in open circuit voltage (<em>V</em><small><sub>oc</sub></small>) and short circuit current (<em>J</em><small><sub>sc</sub></small>). <em>V</em><small><sub>oc</sub></small> increase is due to improved valence band offset between CdTe and NiO. The large conduction band offset also reflects minority carriers away from the CdTe/NiO interface and reduces interface recombination. SCAPS simulations demonstrated that an increase in valence band offset has shown pronounced effects of both s-kinks and rollover.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00125g?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141196946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intrinsic effects of electrolytes on lithium metal deposition and dissolution investigated through a separator-free cell† 通过无隔膜电池研究电解质对锂金属沉积和溶解的内在影响
IF 3.2
Energy advances Pub Date : 2024-05-29 DOI: 10.1039/D4YA00245H
Tomoki Takahashi, Di Wang, Jinkwang Hwang and Kazuhiko Matsumoto
{"title":"Intrinsic effects of electrolytes on lithium metal deposition and dissolution investigated through a separator-free cell†","authors":"Tomoki Takahashi, Di Wang, Jinkwang Hwang and Kazuhiko Matsumoto","doi":"10.1039/D4YA00245H","DOIUrl":"10.1039/D4YA00245H","url":null,"abstract":"<p >Lithium metal batteries are a significant promise for next-generation energy storage due to their high energy density. However, challenges persist in their commercialization stemming from issues during the lithium deposition/dissolution processes, such as low Coulombic efficiency, dendrite formation, and dead-lithium formation. Addressing these challenges requires careful electrolyte design to enhance the reversibility of the lithium metal negative electrode by modifying solvation structures and engineering interfaces. The Coulombic efficiency of lithium deposition/dissolution is one of the most crucial factors in evaluating the performance of electrolytes toward lithium metal, although this is influenced by various factors. In this study, a separator-free cell is adopted to minimize extraneous influences and focus on assessing the intrinsic effects of electrolytes on lithium deposition/dissolution. 48 different electrolytes based on three salts of Li[PF<small><sub>6</sub></small>], Li[FSA] and Li[TFSA] varying in solvents were investigated with or without additives. Moreover, Raman spectroscopy and X-ray photon spectroscopy enhance the discussion by revealing variations in the major species of solid electrolyte interphase components under different electrolyte conditions.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00245h?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141168686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Additive manufacturing of highly conductive carbon nanotube architectures towards carbon-based flexible thermoelectric generators 增材制造高导电性碳纳米管结构,实现碳基柔性热电发电机
IF 3.2
Energy advances Pub Date : 2024-05-29 DOI: 10.1039/D4YA00182F
Christos K. Mytafides, William J. Wright, Raden Gustinvil, Lazaros Tzounis, George Karalis, Alkiviadis S. Paipetis and Emrah Celik
{"title":"Additive manufacturing of highly conductive carbon nanotube architectures towards carbon-based flexible thermoelectric generators","authors":"Christos K. Mytafides, William J. Wright, Raden Gustinvil, Lazaros Tzounis, George Karalis, Alkiviadis S. Paipetis and Emrah Celik","doi":"10.1039/D4YA00182F","DOIUrl":"10.1039/D4YA00182F","url":null,"abstract":"<p >Moving the fabrication of electronics from the conventional 2D orientation to 3D space, necessitates the use of sophisticated additive manufacturing processes which are capable to deliver multifunctional materials and devices with exceptional spatial resolution. In this study, it is reported the nozzle-guided 3D-printing of highly conductive, epoxy-dispersed, single-walled carbon nanotube (SWCNT) architectures with embedded thermoelectric (TE) properties, capable to exploit significant waste thermal energy from the environment. In order to achieve high-resolution and continuous printing with the SWCNT-based paste through a confined nozzle geometry, <em>i.e.</em> without agglomeration and nozzle clogging, a homogeneous epoxy resin-dispersed SWCNT paste was produced. As a result, various 3D-printed structures with high SWCNT concentration (10 wt%) were obtained <em>via</em> shear-mixing processes. The 3D printed p- and n-type epoxy-dispersed SWCNT-based thermoelements exhibit high power factors of 102 and 75 μW mK<small><sup>−2</sup></small>, respectively. The manufactured 3D carbon-based thermoelectric generator (3D-CTEG) has the ability to stably operate at temperatures up to 180 °C in ambient conditions (1 atm, relative humidity: 50 ± 5% RH), obtaining TE values of an open-circuit voltage <em>V</em><small><sub>OC</sub></small> = 13.6 mV, short-circuit current <em>I</em><small><sub>SC</sub></small> = 1204 μA, internal resistance <em>R</em><small><sub>TEG</sub></small> = 11.3 Ohm, and a generated power output <em>P</em><small><sub>max</sub></small> = 4.1 μW at Δ<em>T</em> = 100 K (with <em>T</em><small><sub>Cold</sub></small> = 70 °C). The approach and methodology described in this study aims to increase the flexibility of integration and additive manufacturing processes for advanced 3D-printed conceptual devices and the development of multifunctional materials.</p>","PeriodicalId":72913,"journal":{"name":"Energy advances","volume":null,"pages":null},"PeriodicalIF":3.2,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ya/d4ya00182f?page=search","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141173408","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Performance evaluation of a newly developed transition metal-doped HZSM-5 zeolite catalyst for single-step conversion of C1–C3 alcohols to fuel-range hydrocarbons† 新开发的掺杂过渡金属的 HZSM-5 沸石催化剂在将 C1-C3 醇单步转化为燃料级碳氢化合物中的性能评估
Energy advances Pub Date : 2024-05-29 DOI: 10.1039/D3YA00460K
Ifeanyi Michael Smarte Anekwe, Bilainu Oboirien and Yusuf Makarfi Isa
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