Pub Date : 2024-09-24DOI: 10.1016/j.mtsust.2024.100989
Xin Huang , Kang Xu , Jiahao Li , Wei Chen , Zhenxing Yang , Kebin Ding , Yujie Leng , Yakui Weng , Shuai Dong , Yunhui Wang , Zhihong Yang
The rational design of van der Waals heterostructure offers an effective avenue for improving the photocatalytic efficiency of individual two-dimensional materials, garnering extensive interest in recent years. Herein, the feasibility of GeC/Ga2SO heterostructure as a photocatalyst for overall water splitting has been explored based on the first-principles calculations. Our findings reveal that the electronic bandstructure of GeC/Ga2SO heterostructure can be engineered in staggered or straddling band alignment depending on stacking patterns. Particularly, in the GeC/Ga2SO heterostructure with staggered band alignment, an intrinsic built-in electric field is established at the interface with the direction from GeC to Ga2SO, facilitating the formation of a direct Z-scheme heterostructure. Also importantly, the band-edge positions of Z-scheme GeC/Ga2SO heterostructure cross the water redox potentials, providing adequate driving force for both the reduction and oxidation reactions of water. Gibbs free energy calculations demonstrated that the photocatalytic overall water splitting can proceed spontaneously in the neutral environment (pH = 7) under light irradiation. Moreover, GeC/Ga2SO heterostructure exhibits good thermal stability and a strong (magnitude in 105 cm−1) and broad (from visible to ultraviolet light) optical absorption. Finally, through applying the tensile strain, further enhancements in the optical absorption and carrier redox ability are achieved due to the favorable modulation in the bandgap. Therefore, all these features make GeC/Ga2SO heterostructure show great potential in the application of photocatalytic water splitting.
{"title":"First-principles study of GeC/Ga2SO heterostructure as a potential direct Z-scheme photocatalyst for water splitting","authors":"Xin Huang , Kang Xu , Jiahao Li , Wei Chen , Zhenxing Yang , Kebin Ding , Yujie Leng , Yakui Weng , Shuai Dong , Yunhui Wang , Zhihong Yang","doi":"10.1016/j.mtsust.2024.100989","DOIUrl":"10.1016/j.mtsust.2024.100989","url":null,"abstract":"<div><div>The rational design of van der Waals heterostructure offers an effective avenue for improving the photocatalytic efficiency of individual two-dimensional materials, garnering extensive interest in recent years. Herein, the feasibility of GeC/Ga<sub>2</sub>SO heterostructure as a photocatalyst for overall water splitting has been explored based on the first-principles calculations. Our findings reveal that the electronic bandstructure of GeC/Ga<sub>2</sub>SO heterostructure can be engineered in staggered or straddling band alignment depending on stacking patterns. Particularly, in the GeC/Ga<sub>2</sub>SO heterostructure with staggered band alignment, an intrinsic built-in electric field is established at the interface with the direction from GeC to Ga<sub>2</sub>SO, facilitating the formation of a direct Z-scheme heterostructure. Also importantly, the band-edge positions of Z-scheme GeC/Ga<sub>2</sub>SO heterostructure cross the water redox potentials, providing adequate driving force for both the reduction and oxidation reactions of water. Gibbs free energy calculations demonstrated that the photocatalytic overall water splitting can proceed spontaneously in the neutral environment (pH = 7) under light irradiation. Moreover, GeC/Ga<sub>2</sub>SO heterostructure exhibits good thermal stability and a strong (magnitude in 10<sup>5</sup> cm<sup>−1</sup>) and broad (from visible to ultraviolet light) optical absorption. Finally, through applying the tensile strain, further enhancements in the optical absorption and carrier redox ability are achieved due to the favorable modulation in the bandgap. Therefore, all these features make GeC/Ga<sub>2</sub>SO heterostructure show great potential in the application of photocatalytic water splitting.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100989"},"PeriodicalIF":7.1,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142359015","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-24DOI: 10.1016/j.mtsust.2024.100992
Minh-Trang Huynh Pham , Art Wei Yao Ang , Truong-Giang Vo , Tomohiro Hayashi , Chia-Ying Chiang
The burgeoning interest in the electrocatalytic conversion of biomass-derived compounds, exemplified by 5-hydroxymethylfurfural (HMF), into economically valuable products underscores the significance of such studies. Within this context, the electrocatalytic oxidation of HMF into 2,5-diformylfuran (DFF) using the mixed-valence silver (I, III) oxide (AgO) as the catalyst is presented for the first time. A thorough investigation has been carried out to explore the complex factors influencing the electrochemical transformation of the HMF to DFF, involving applied potentials, reactant concentrations, and the significant implications of mass transfer phenomena. Under optimized conditions, DFF, one of the highest value-added intermediates, can be produced with selectivity as high as 54%. Additionally, a yield of 10.8 μmol cm−2 h−1 was obtained under mild basic condition. Another pivotal aspect of this work involves meticulously examining the reaction process, bolstered by a comprehensive analytical approach that integrates high-performance liquid chromatography (HPLC), and operando Raman spectroscopy. The amalgamation of operando Raman spectroscopy with advanced simulation techniques represents a novel endeavor, offering a groundbreaking pathway to unravel the complexities inherent in these compounds and contribute substantially to the understanding of HMF oxidation and its intermediates. By looking closely at the catalyst surface during the reaction, a valuable insight into the steps involved was developed, helping in proposing an in-depth reaction pathway.
{"title":"Unlocking the potential of mixed-valence silver oxide for electrochemical valorization of 5-hydroxymethylfurfural into valuable products","authors":"Minh-Trang Huynh Pham , Art Wei Yao Ang , Truong-Giang Vo , Tomohiro Hayashi , Chia-Ying Chiang","doi":"10.1016/j.mtsust.2024.100992","DOIUrl":"10.1016/j.mtsust.2024.100992","url":null,"abstract":"<div><div>The burgeoning interest in the electrocatalytic conversion of biomass-derived compounds, exemplified by 5-hydroxymethylfurfural (HMF), into economically valuable products underscores the significance of such studies. Within this context, the electrocatalytic oxidation of HMF into 2,5-diformylfuran (DFF) using the mixed-valence silver (I, III) oxide (AgO) as the catalyst is presented for the first time. A thorough investigation has been carried out to explore the complex factors influencing the electrochemical transformation of the HMF to DFF, involving applied potentials, reactant concentrations, and the significant implications of mass transfer phenomena. Under optimized conditions, DFF, one of the highest value-added intermediates, can be produced with selectivity as high as 54%. Additionally, a yield of 10.8 μmol cm<sup>−2</sup> h<sup>−1</sup> was obtained under mild basic condition. Another pivotal aspect of this work involves meticulously examining the reaction process, bolstered by a comprehensive analytical approach that integrates high-performance liquid chromatography (HPLC), and <em>operando</em> Raman spectroscopy. The amalgamation of <em>operando</em> Raman spectroscopy with advanced simulation techniques represents a novel endeavor, offering a groundbreaking pathway to unravel the complexities inherent in these compounds and contribute substantially to the understanding of HMF oxidation and its intermediates. By looking closely at the catalyst surface during the reaction, a valuable insight into the steps involved was developed, helping in proposing an in-depth reaction pathway.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100992"},"PeriodicalIF":7.1,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142327485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-24DOI: 10.1016/j.mtsust.2024.100993
Deepu Murukadas , Woongki Lee , Chanbin Park , Hwajeong Kim , Youngkyoo Kim
Here we report that organic/inorganic hybrid composite films, consisting of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and zeolite Y (Zy), can efficiently convert heat to electricity in the horizontal device geometry. The PEDOT:PSS/Zy (PPZy) hybrid composite films were prepared from corresponding aqueous solutions at various Zy contents (up to 50 wt%). The PPZy solutions exhibited an increased viscous state with a maximum at Zy = 30 wt%, indicating strong interactions between PEDOT:PSS and Zy components. All devices with the PPZy composite films could convert heat to electricity and showed higher thermoelectric (TE) performances than those with the pristine PEDOT:PSS films. The TE devices with the PPZy films (Zy = 30 wt%) delivered an output power of 8.8 pW with a power factor of 0.76 μW/mK2, which is ca. 20 times higher than those with the pristine PEDOT:PSS films. The flexible TE devices, which were fabricated on poly(ethylene naphthalate) (PEN) film substrates, exhibited robust TE performances even after 5000 bending cycles. The present approach of hybrid composite films based on zeolite particles may contribute to further TE performance improvement for flexible and wearable TE devices.
在此,我们报告了由聚(3,4-亚乙二氧基噻吩):聚(苯乙烯磺酸)(PEDOT:PSS)和沸石 Y(Zy)组成的有机/无机混合复合薄膜可以在水平器件几何形状中有效地将热能转化为电能。PEDOT:PSS/Zy (PPZy) 混合复合薄膜是用不同 Zy 含量(最高达 50 wt%)的相应水溶液制备的。PPZy 溶液的粘度在 Zy = 30 wt% 时达到最大值,表明 PEDOT:PSS 和 Zy 成分之间存在很强的相互作用。与使用原始 PEDOT:PSS 薄膜的器件相比,使用 PPZy 复合薄膜的所有器件都能将热量转化为电能,并显示出更高的热电(TE)性能。使用 PPZy 薄膜(Zy = 30 wt%)的 TE 器件输出功率为 8.8 pW,功率因数为 0.76 μW/mK2,比使用原始 PEDOT:PSS 薄膜的器件高出约 20 倍。在聚(萘乙酸乙二醇酯)(PEN)薄膜基底上制作的柔性 TE 器件即使在经过 5000 次弯曲循环后仍能表现出稳定的 TE 性能。目前基于沸石颗粒的混合复合薄膜方法可能有助于进一步提高柔性和可穿戴 TE 器件的 TE 性能。
{"title":"Thermoelectric devices with polymer/zeolite hybrid composite films for conversion of heat to electricity","authors":"Deepu Murukadas , Woongki Lee , Chanbin Park , Hwajeong Kim , Youngkyoo Kim","doi":"10.1016/j.mtsust.2024.100993","DOIUrl":"10.1016/j.mtsust.2024.100993","url":null,"abstract":"<div><div>Here we report that organic/inorganic hybrid composite films, consisting of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and zeolite Y (Zy), can efficiently convert heat to electricity in the horizontal device geometry. The PEDOT:PSS/Zy (PPZy) hybrid composite films were prepared from corresponding aqueous solutions at various Zy contents (up to 50 wt%). The PPZy solutions exhibited an increased viscous state with a maximum at Zy = 30 wt%, indicating strong interactions between PEDOT:PSS and Zy components. All devices with the PPZy composite films could convert heat to electricity and showed higher thermoelectric (TE) performances than those with the pristine PEDOT:PSS films. The TE devices with the PPZy films (Zy = 30 wt%) delivered an output power of 8.8 pW with a power factor of 0.76 μW/mK<sup>2</sup>, which is ca. 20 times higher than those with the pristine PEDOT:PSS films. The flexible TE devices, which were fabricated on poly(ethylene naphthalate) (PEN) film substrates, exhibited robust TE performances even after 5000 bending cycles. The present approach of hybrid composite films based on zeolite particles may contribute to further TE performance improvement for flexible and wearable TE devices.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100993"},"PeriodicalIF":7.1,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142359017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-23DOI: 10.1016/j.mtsust.2024.100987
Wei Dong , Zhiqiang Ren , Xin Liu
As an efficient method for utilizing coal gangue (CG), concrete incorporating coal gangue as coarse aggregate has significantly reduced the reliance on natural aggregates, offering substantial environmental and economic benefits. In this study, coal gangue concrete was prepared with coal gangue replacement rates of 0, 20, 40, 60, 80, and 100%, and mechanical tests under unconfined compression were conducted to evaluate the stress-strain behavior and failure mechanism of coal gangue coarse aggregate concrete (CGC). Utilizing scanning electron microscope (SEM) microscopic characterization, the microscopic failure mechanism of CGC was further elucidated. With increased coal gangue replacement, the CGC's uniaxial compression failure mode shifts from shear to longitudinal splitting failure. The slope, peak stress and elastic modulus of the stress–strain curve's rising section are negatively correlated with the coal gangue content, while the falling section's slope, peak strain and ultimate strain are positively correlated. Next, building upon the classical constitutive model, we adjust the constitutive parameters utilizing the uniaxial compressive strength and coal gangue content. Finally, we introduce a predictive model for the CGC's constitutive compressive behavior across various content levels. There is a notably high agreement between the model and experimental data.
{"title":"Experimental study on constitutive relation of coal gangue coarse aggregate concrete under uniaxial compression","authors":"Wei Dong , Zhiqiang Ren , Xin Liu","doi":"10.1016/j.mtsust.2024.100987","DOIUrl":"10.1016/j.mtsust.2024.100987","url":null,"abstract":"<div><div>As an efficient method for utilizing coal gangue (CG), concrete incorporating coal gangue as coarse aggregate has significantly reduced the reliance on natural aggregates, offering substantial environmental and economic benefits. In this study, coal gangue concrete was prepared with coal gangue replacement rates of 0, 20, 40, 60, 80, and 100%, and mechanical tests under unconfined compression were conducted to evaluate the stress-strain behavior and failure mechanism of coal gangue coarse aggregate concrete (CGC). Utilizing scanning electron microscope (SEM) microscopic characterization, the microscopic failure mechanism of CGC was further elucidated. With increased coal gangue replacement, the CGC's uniaxial compression failure mode shifts from shear to longitudinal splitting failure. The slope, peak stress and elastic modulus of the stress–strain curve's rising section are negatively correlated with the coal gangue content, while the falling section's slope, peak strain and ultimate strain are positively correlated. Next, building upon the classical constitutive model, we adjust the constitutive parameters utilizing the uniaxial compressive strength and coal gangue content. Finally, we introduce a predictive model for the CGC's constitutive compressive behavior across various content levels. There is a notably high agreement between the model and experimental data.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100987"},"PeriodicalIF":7.1,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142315570","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-23DOI: 10.1016/j.mtsust.2024.100986
Shu-Yao Li , Ting Yan , Ying-Jie Huo , Wei-Guo Pan
Combining solar energy conversion with latent heat storage based on phase change materials (PCMs) has offered a promising way for expanding solar energy utilization. However, the application of PCMs for solar heat utilization is greatly limited by low thermal conductivity and poor sunlight absorption capacity. Carbon foam (CF) has excellent sunlight absorption properties, and carbon nanotube (CNT) have good thermal conductivity. In this study, CF/CNT porous material was prepared by self-assembly thermal-bridge between CF and CNT. CF/CNT was employed to a porous matrix for the encapsulation of octadecanol (OC), and then a composite photothermal PCM (CF/CNT/OC) was successfully fabricated. Compared with pure OC, the CF/CNT/OC has superior thermal conductivity capacity and excellent photothermal conversion performance. The thermal conductivity of CF/CNT/OC89 reached 1.31 W m−1 K−1, and the photothermal conversion efficiency was 82.6 %. Meanwhile, the melting enthalpy of CF/CNT/OC98 reached up to 275.8 kJ∙kg−1, exhibiting the excellent thermal storage properties. This functional composite PCM has broad application prospects in solar energy capture and storage, building energy saving and so on.
{"title":"Carbon nanotube/carbon foam thermal-bridge enhancing solar energy conversion and storage of phase change materials","authors":"Shu-Yao Li , Ting Yan , Ying-Jie Huo , Wei-Guo Pan","doi":"10.1016/j.mtsust.2024.100986","DOIUrl":"10.1016/j.mtsust.2024.100986","url":null,"abstract":"<div><div>Combining solar energy conversion with latent heat storage based on phase change materials (PCMs) has offered a promising way for expanding solar energy utilization. However, the application of PCMs for solar heat utilization is greatly limited by low thermal conductivity and poor sunlight absorption capacity. Carbon foam (CF) has excellent sunlight absorption properties, and carbon nanotube (CNT) have good thermal conductivity. In this study, CF/CNT porous material was prepared by self-assembly thermal-bridge between CF and CNT. CF/CNT was employed to a porous matrix for the encapsulation of octadecanol (OC), and then a composite photothermal PCM (CF/CNT/OC) was successfully fabricated. Compared with pure OC, the CF/CNT/OC has superior thermal conductivity capacity and excellent photothermal conversion performance. The thermal conductivity of CF/CNT/OC89 reached 1.31 W m<sup>−1</sup> K<sup>−1</sup>, and the photothermal conversion efficiency was 82.6 %. Meanwhile, the melting enthalpy of CF/CNT/OC98 reached up to 275.8 kJ∙kg<sup>−1</sup>, exhibiting the excellent thermal storage properties. This functional composite PCM has broad application prospects in solar energy capture and storage, building energy saving and so on.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100986"},"PeriodicalIF":7.1,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142359011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-23DOI: 10.1016/j.mtsust.2024.100985
Youssef Miyah , Noureddine El Messaoudi , Mohammed Benjelloun , Jordana Georgin , Dison Stracke Pfingsten Franco , Yaser Acikbas , Heri Septya Kusuma , Mika Sillanpää
This review article summarizes current developments in the design and application of metal-organic framework (MOF)-derived magnetic nanocomposites (MNCs) to remove organic pollutants (OPs) in water efficiently. In the review, various methods for synthesis, like in-situ encapsulation and post-synthetic modification, have been discussed, showing how magnetic nanoparticles incorporated into MOFs resulted in materials that had improved adsorption and advanced oxidation processes. These NCs showed unique structural characteristics and functional advantages given their large surface area, tunable pore sizes, and magnetic separability. This work has emphasized dual functionality concerning adsorption and photocatalytic degradation. More importantly, these processes synergistically cooperate to realize considerably high removal efficiencies for a wide range of OPs. It also addresses current challenges on stability and scalability issues and proposes possible ways of improving MOF-MNCs' performance. This is followed by future research directions on the betterment of the practical application of MOF-MNCs in controlling water pollution, highlighting their potential as a feasible and effective solution for mitigating water contamination. Lastly, it is proposed in this synthesis that Ishikawa 5Ms should be considered when developing low-cost MOF-MNCs and industrializing their application for water depollution.
{"title":"MOF-derived magnetic nanocomposites as potential formulations for the efficient removal of organic pollutants from water via adsorption and advanced oxidation processes: A review","authors":"Youssef Miyah , Noureddine El Messaoudi , Mohammed Benjelloun , Jordana Georgin , Dison Stracke Pfingsten Franco , Yaser Acikbas , Heri Septya Kusuma , Mika Sillanpää","doi":"10.1016/j.mtsust.2024.100985","DOIUrl":"10.1016/j.mtsust.2024.100985","url":null,"abstract":"<div><div>This review article summarizes current developments in the design and application of metal-organic framework (MOF)-derived magnetic nanocomposites (MNCs) to remove organic pollutants (OPs) in water efficiently. In the review, various methods for synthesis, like in-situ encapsulation and post-synthetic modification, have been discussed, showing how magnetic nanoparticles incorporated into MOFs resulted in materials that had improved adsorption and advanced oxidation processes. These NCs showed unique structural characteristics and functional advantages given their large surface area, tunable pore sizes, and magnetic separability. This work has emphasized dual functionality concerning adsorption and photocatalytic degradation. More importantly, these processes synergistically cooperate to realize considerably high removal efficiencies for a wide range of OPs. It also addresses current challenges on stability and scalability issues and proposes possible ways of improving MOF-MNCs' performance. This is followed by future research directions on the betterment of the practical application of MOF-MNCs in controlling water pollution, highlighting their potential as a feasible and effective solution for mitigating water contamination. Lastly, it is proposed in this synthesis that Ishikawa 5Ms should be considered when developing low-cost MOF-MNCs and industrializing their application for water depollution.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100985"},"PeriodicalIF":7.1,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142315571","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-21DOI: 10.1016/j.mtsust.2024.100984
Se Jung Lee , Jong-Beom Baek , In-Yup Jeon
Triazine graphitic nanoplatelets (TGNP) were synthesized as an anchor to improve the activity and stability of Pt nanoparticles for the hydrogen evolution reaction (HER). Pt@TGNP, Pt supported on TGNP, showed high performance (i.e., high activity and stability) for HER under acidic conditions. Although Pt@TGNP contained very low Pt content (8.7 wt%), it exhibited much better activity (overpotential: 32 mV, Tafel slope: 28.4 mV dec−1) and stability (overpotential increase: 1.6 mV) for HER, compared with Pt/C (overpotential: 35 mV, Tafel slope: 29.2 mV dec−1, and overpotential increase: 6.2 mV). The results convincingly demonstrate that the triazine units of TGNP offer active sites that increase catalytic activity, as well as anchoring sites to prevent the aggregation of Pt nanoparticles. Results confirmed that Pt@TGNP with its efficient catalytic activity and stability is a promising alternative to existing Pt-based catalysts, and TGNP with triazine is highly likely to be utilized as a catalyst support in various applications.
{"title":"Improving HER activity and stability of Pt nanoparticle on Triazine graphitic nanoplatelets","authors":"Se Jung Lee , Jong-Beom Baek , In-Yup Jeon","doi":"10.1016/j.mtsust.2024.100984","DOIUrl":"10.1016/j.mtsust.2024.100984","url":null,"abstract":"<div><div>Triazine graphitic nanoplatelets (TGNP) were synthesized as an anchor to improve the activity and stability of Pt nanoparticles for the hydrogen evolution reaction (HER). Pt@TGNP, Pt supported on TGNP, showed high performance (<em>i.e.,</em> high activity and stability) for HER under acidic conditions. Although Pt@TGNP contained very low Pt content (8.7 wt%), it exhibited much better activity (overpotential: 32 mV, Tafel slope: 28.4 mV dec<sup>−1</sup>) and stability (overpotential increase: 1.6 mV) for HER, compared with Pt/C (overpotential: 35 mV, Tafel slope: 29.2 mV dec<sup>−1</sup>, and overpotential increase: 6.2 mV). The results convincingly demonstrate that the triazine units of TGNP offer active sites that increase catalytic activity, as well as anchoring sites to prevent the aggregation of Pt nanoparticles. Results confirmed that Pt@TGNP with its efficient catalytic activity and stability is a promising alternative to existing Pt-based catalysts, and TGNP with triazine is highly likely to be utilized as a catalyst support in various applications.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100984"},"PeriodicalIF":7.1,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142315569","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-21DOI: 10.1016/j.mtsust.2024.100982
Sikandar Aftab , Burragoni Sravanthi Goud , Maria Mukhtar , Zeeshan Haider , Fahmid Kabir , Ghazanfar Nazir , Muhammad Jehanzaib Aslam , Muhammad Aslam , H.H. Hegazy , Jae Hong Kim , Altaf Hussain Rajpar
One practical solution for effective solar energy conversion is the use of perovskite photovoltaics (PV). Nevertheless, issues like hysteresis, instability, and short device lifetimes have restricted their practical use. As interfacial layers, two-dimensional transition metal dichalcogenides (TMDs) are quite different from metal oxides and small molecules. Optical and electronic properties can be improved by adjusting layers or applying strain on TMDs, which have a layered structure with direct bandgaps that is atomically thin. High carrier mobilities and distinct van der Waals interactions with neighboring layers are also supported by them. Charge transport capabilities; on the other hand, small molecules are typically processed using solution-based techniques and provide discrete energy levels. Interfacial layers facilitate smooth charge transport, which is advantageous to perovskite absorber layers. Much attention has been paid to the unique properties and compatibility of 2D TMDs with perovskite solar cells. The use of 2D TMDs materials as interfacial layers in perovskite photovoltaics (PVs) is reviewed in this review, with particular attention paid to their roles as electron transport layers (ETLs) and hole transport layers (HTLs). We first describe the main challenges faced by PSCs and how interfacial layers offer workable solutions. We also study the ways in which these layers improve robustness of the device, reduce hysteresis effects, and increase charge extraction efficiency. We consolidate information regarding the potential of two-dimensional (2D) materials to address important concerns concerning PSCs, thereby advancing the development of dependable and effective PVC devices for real-world solar energy harvesting applications. We do this by providing a comprehensive overview of recent research.
{"title":"Perovskite photovoltaics with cutting-edge strategies in 2D TMDs-based interfacial layer optimization","authors":"Sikandar Aftab , Burragoni Sravanthi Goud , Maria Mukhtar , Zeeshan Haider , Fahmid Kabir , Ghazanfar Nazir , Muhammad Jehanzaib Aslam , Muhammad Aslam , H.H. Hegazy , Jae Hong Kim , Altaf Hussain Rajpar","doi":"10.1016/j.mtsust.2024.100982","DOIUrl":"10.1016/j.mtsust.2024.100982","url":null,"abstract":"<div><div>One practical solution for effective solar energy conversion is the use of perovskite photovoltaics (PV). Nevertheless, issues like hysteresis, instability, and short device lifetimes have restricted their practical use. As interfacial layers, two-dimensional transition metal dichalcogenides (TMDs) are quite different from metal oxides and small molecules. Optical and electronic properties can be improved by adjusting layers or applying strain on TMDs, which have a layered structure with direct bandgaps that is atomically thin. High carrier mobilities and distinct van der Waals interactions with neighboring layers are also supported by them. Charge transport capabilities; on the other hand, small molecules are typically processed using solution-based techniques and provide discrete energy levels. Interfacial layers facilitate smooth charge transport, which is advantageous to perovskite absorber layers. Much attention has been paid to the unique properties and compatibility of 2D TMDs with perovskite solar cells. The use of 2D TMDs materials as interfacial layers in perovskite photovoltaics (PVs) is reviewed in this review, with particular attention paid to their roles as electron transport layers (ETLs) and hole transport layers (HTLs). We first describe the main challenges faced by PSCs and how interfacial layers offer workable solutions. We also study the ways in which these layers improve robustness of the device, reduce hysteresis effects, and increase charge extraction efficiency. We consolidate information regarding the potential of two-dimensional (2D) materials to address important concerns concerning PSCs, thereby advancing the development of dependable and effective PVC devices for real-world solar energy harvesting applications. We do this by providing a comprehensive overview of recent research.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100982"},"PeriodicalIF":7.1,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142312562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-19DOI: 10.1016/j.mtsust.2024.100981
Chandu V.V.Muralee Gopi , Salem Alzahmi , Mohammad Y. Al-Haik , Yedluri Anil Kumar , Fathalla Hamed , Yousef Haik , Ihab M. Obaidat
The demand for high-power and energy-dense electrochemical energy storage solutions has led to the utilization of pseudocapacitive materials. These materials store charges by undergoing Faradaic reactions at or near the electrode surfaces. They offer higher energy density than electric double-layer capacitors while maintaining the rapid charging/discharging capabilities characteristic of supercapacitors. This review delves into the synergistic relationship between transition metal oxides (TMOs) and carbon-based materials to create advanced supercapacitors. Combining the pseudocapacitive properties of TMOs with the high conductivity and carbon surface area, hybrid composites offer the potential to bridge the gap between energy and power density. The review comprehensively explores a range of TMOs, including ZnO, NiO, CoO, CuO, MnO2, and RuO2, and their integration with various carbon architectures. Key synthesis techniques, characterization methods, and electrochemical performance metrics are discussed to comprehensively understand these materials. Moreover, the review highlights recent advancements and identifies critical challenges to guide future research efforts toward developing high-performance and commercially viable supercapacitors based on TMO/carbon composites.
{"title":"Recent advances in pseudocapacitive electrode materials for high energy density aqueous supercapacitors: Combining transition metal oxides with carbon nanomaterials","authors":"Chandu V.V.Muralee Gopi , Salem Alzahmi , Mohammad Y. Al-Haik , Yedluri Anil Kumar , Fathalla Hamed , Yousef Haik , Ihab M. Obaidat","doi":"10.1016/j.mtsust.2024.100981","DOIUrl":"10.1016/j.mtsust.2024.100981","url":null,"abstract":"<div><div>The demand for high-power and energy-dense electrochemical energy storage solutions has led to the utilization of pseudocapacitive materials. These materials store charges by undergoing Faradaic reactions at or near the electrode surfaces. They offer higher energy density than electric double-layer capacitors while maintaining the rapid charging/discharging capabilities characteristic of supercapacitors. This review delves into the synergistic relationship between transition metal oxides (TMOs) and carbon-based materials to create advanced supercapacitors. Combining the pseudocapacitive properties of TMOs with the high conductivity and carbon surface area, hybrid composites offer the potential to bridge the gap between energy and power density. The review comprehensively explores a range of TMOs, including ZnO, NiO, CoO, CuO, MnO<sub>2</sub>, and RuO<sub>2</sub>, and their integration with various carbon architectures. Key synthesis techniques, characterization methods, and electrochemical performance metrics are discussed to comprehensively understand these materials. Moreover, the review highlights recent advancements and identifies critical challenges to guide future research efforts toward developing high-performance and commercially viable supercapacitors based on TMO/carbon composites.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100981"},"PeriodicalIF":7.1,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142312597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-16DOI: 10.1016/j.mtsust.2024.100976
Yixuan Han , Tong Lyu , Yanpeng Wang , Zhiwei Fu , Deliang Li , Ruonan Liu , He Liu , Ziya Gao , Huilin Yuan , Ye Tian
Improving thermoelectric generators (TEGs) performance remains challenging in the context of energy crisis and thermal-pollution. Here, we present a strategy for thermal management and performance enhancement of TEGs by sustainable evaporative cooling utilizing highly hygroscopic and adhesive ionogels (PIGs). Rational swelling and poly-[2-(Methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (PDMAPS) chains with group interactions prevent lithium chloride (LiCl) and 1-ethyl-3-methylimidazolium acetate ([EMIM][Ac]) leakage, while carbon nanotubes (CNTs) and MIL-101(Cr) optimize the evaporative cooling of PIGs. PIGs possess high sorption (252.72% at 25 °C, 90% RH for 12 h) and steady sorption-desorption kinetics. Meanwhile, PIGs exhibit high adhesion (130.89 N m−1) on TEGs. The evaporative cooling of PIGs enhances the temperature difference of TEGs. The potential of PIG-TEG is increased by three times at heat source temperatures of 50–80 °C, and the output power density stabilizes at ∼706.25 mW m−2 after heating at 50 °C for 1 h. Moreover, the PIG-TEG maintains stable output enhancement for prolonged time (over 24 h). Additionally, we integrate PIG-TEGs for the durable power supply of devices and design a movable model car, which utilizes waste heat for self-powering. PIGs realize effective thermoelectric output enhancement of TEGs, and provide ideas in clean energy conversion, wearable devices, and mobile power.
{"title":"Hygroscopic ionogel for enhanced thermoelectric generation performance","authors":"Yixuan Han , Tong Lyu , Yanpeng Wang , Zhiwei Fu , Deliang Li , Ruonan Liu , He Liu , Ziya Gao , Huilin Yuan , Ye Tian","doi":"10.1016/j.mtsust.2024.100976","DOIUrl":"10.1016/j.mtsust.2024.100976","url":null,"abstract":"<div><p>Improving thermoelectric generators (TEGs) performance remains challenging in the context of energy crisis and thermal-pollution. Here, we present a strategy for thermal management and performance enhancement of TEGs by sustainable evaporative cooling utilizing highly hygroscopic and adhesive ionogels (PIGs). Rational swelling and poly-[2-(Methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (PDMAPS) chains with group interactions prevent lithium chloride (LiCl) and 1-ethyl-3-methylimidazolium acetate ([EMIM][Ac]) leakage, while carbon nanotubes (CNTs) and MIL-101(Cr) optimize the evaporative cooling of PIGs. PIGs possess high sorption (252.72% at 25 °C, 90% RH for 12 h) and steady sorption-desorption kinetics. Meanwhile, PIGs exhibit high adhesion (130.89 N m<sup>−1</sup>) on TEGs. The evaporative cooling of PIGs enhances the temperature difference of TEGs. The potential of PIG-TEG is increased by three times at heat source temperatures of 50–80 °C, and the output power density stabilizes at ∼706.25 mW m<sup>−2</sup> after heating at 50 °C for 1 h. Moreover, the PIG-TEG maintains stable output enhancement for prolonged time (over 24 h). Additionally, we integrate PIG-TEGs for the durable power supply of devices and design a movable model car, which utilizes waste heat for self-powering. PIGs realize effective thermoelectric output enhancement of TEGs, and provide ideas in clean energy conversion, wearable devices, and mobile power.</p></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"28 ","pages":"Article 100976"},"PeriodicalIF":7.1,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142272101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}