Applied Catalysis B: Environment and Energy最新文献

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Boosting hydrogenation properties of supported Cu-based catalysts by replacing Cu0 active sites 通过替换 Cu0 活性位点提高支撑铜基催化剂的氢化性能
Applied Catalysis B: Environment and Energy Pub Date : 2024-09-03 DOI: 10.1016/j.apcatb.2024.124563
Bo Kang, Zhilin Chen, Jie Yang, Mingxin Lv, Hongli He, Guoxin Chen, Liyuan Huai, Chunlin Chen, Jian Zhang
{"title":"Boosting hydrogenation properties of supported Cu-based catalysts by replacing Cu0 active sites","authors":"Bo Kang, Zhilin Chen, Jie Yang, Mingxin Lv, Hongli He, Guoxin Chen, Liyuan Huai, Chunlin Chen, Jian Zhang","doi":"10.1016/j.apcatb.2024.124563","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124563","url":null,"abstract":"Balancing the Cu/Cu ratio is a common strategy to improve catalytic activity of Cu-based catalysts but is still constrained by low atomic utilization and the inherent nature of charge distribution. Herein, we reported a strategy of replacing the Cu active sites in Cu-based catalysts by constructing bimetallic sites on ceria, which consist of spatially separated trace amounts of palladium metal and plate-shaped Cu clusters with one-atom layers. The catalytic activity of the prepared CuPd/CeO-FA catalyst (using formic acid) was 4 times that of conventional CuPd/CeO-H catalyst in selective hydrogenation of 5-hydroxymethylfurfural to 2,5-bis(hydroxymethyl)furan, even outperforming some existing noble metal catalysts. Multiple characterizations and theoretical calculations demonstrated that the Pd atom is the heterolytic activation site for H molecules while plate-shaped Cu metal clusters act as effective hydrogenation places. This directional control involving both spatial relationship and electronic structure of the active site provides a new strategy for designing hydrogenated catalysts.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A highly active and stable palladium zeolite catalyst for wet methane combustion 用于湿式甲烷燃烧的高活性、高稳定性钯沸石催化剂
Applied Catalysis B: Environment and Energy Pub Date : 2024-09-03 DOI: 10.1016/j.apcatb.2024.124562
Xuechao Tan, Suk Bong Hong
{"title":"A highly active and stable palladium zeolite catalyst for wet methane combustion","authors":"Xuechao Tan, Suk Bong Hong","doi":"10.1016/j.apcatb.2024.124562","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124562","url":null,"abstract":"Natural gas engines are the most viable alternative to diesel and gasoline ones. However, the current state-of-art catalyst, palladium (Pd) on alumina, for eliminating unburnt methane from engine exhaust suffers from high light-off temperature (> 400 °C) and poor water tolerance. Here we systematically investigated the effects of zeolite structure and Si/Al ratio, catalyst calcination temperature and extra-framework cation type on catalytic performance of zeolite-supported Pd catalysts for wet methane combustion to overcome these limitations. We found that a 3.0 wt% Pd catalyst supported on Na-post-exchanged 500 °C-calcined IWV zeolite with a Si/Al ratio of 45 has a light-off temperature as low as 290 °C for methane combustion in the presence of 10 % water vapor while maintaining ca. 85 % methane conversion at 330 °C for 100 h. This study provides a new direction for bringing supported Pd catalysts close to real-world applications.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"404 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ternary ordered L10-Pt-Co-Fe intermetallics for efficient ORR catalysis through dissociation pathway 通过解离途径实现高效 ORR 催化的三元有序 L10-Pt-Co-Fe 金属间化合物
Applied Catalysis B: Environment and Energy Pub Date : 2024-09-02 DOI: 10.1016/j.apcatb.2024.124556
Yuekun Hu, Mingwang Lu, Guanhua Zhang, Xiaowei Zhao, Yan Liu, Xiaojing Yang, Xiaofei Yu, Xinghua Zhang, Zunming Lu, Lanlan Li
{"title":"Ternary ordered L10-Pt-Co-Fe intermetallics for efficient ORR catalysis through dissociation pathway","authors":"Yuekun Hu, Mingwang Lu, Guanhua Zhang, Xiaowei Zhao, Yan Liu, Xiaojing Yang, Xiaofei Yu, Xinghua Zhang, Zunming Lu, Lanlan Li","doi":"10.1016/j.apcatb.2024.124556","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124556","url":null,"abstract":"Developing efficient and durable Pt-based electrocatalysts for oxygen reduction reaction (ORR) is critical for the practical application of fuel cells but still remains challenge at present. Here we successfully synthesized a series of ternary L1-PtCoFe (x=0.33, 0.50 and 0.67) intermetallic nanoparticles (NPs) supported on reduced graphene oxide for ORR catalysis. L1-PtCoFe exhibits the highest mass activity (MA) of 0.93 A mg at 0.9 V (1.82 times the corresponding binary L1-PtCo intermetallics) and minimal activity loss (24.73 % loss in MA) after 30,000 potential cycles. By Density Functional Theory calculations, the excellent performance of ternary L1-PtCoFe can be ascribed to: (1) more efficient electronic structure regulation caused by dual-element driven electron transfer, which leads to more electron accumulation on Pt and weakens the over-binding of oxygen-containing species, (2) the unique two-center bridge pattern of O adsorption over Pt-Fe site leads to ORR proceeding the dissociative mechanism, avoiding the formation of OOH*.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"48 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205111","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydroxyl-functionalization promoted activity and recovery of ionic liquids in direct dimethyl carbonate synthesis from CO2 羟基官能化促进了二氧化碳直接合成碳酸二甲酯过程中离子液体的活性和回收率
Applied Catalysis B: Environment and Energy Pub Date : 2024-09-02 DOI: 10.1016/j.apcatb.2024.124557
Jiawei Ruan, Lifang Chen, Xinzi Wu, Shaokang Qian, Kunchi Xie, Xiaoyi Zhang, Hongye Cheng, Zhen Song, Zhiwen Qi
{"title":"Hydroxyl-functionalization promoted activity and recovery of ionic liquids in direct dimethyl carbonate synthesis from CO2","authors":"Jiawei Ruan, Lifang Chen, Xinzi Wu, Shaokang Qian, Kunchi Xie, Xiaoyi Zhang, Hongye Cheng, Zhen Song, Zhiwen Qi","doi":"10.1016/j.apcatb.2024.124557","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124557","url":null,"abstract":"Direct synthesis of dimethyl carbonate (DMC) from CO is promising for CO utilization, however its efficiency remains far from industrial-scale implementation for lack of customized catalysts. Herein, a hydroxyl-functionalized ionic liquid (HFIL) was developed to enhance catalytic activity, and importantly, to facilitate IL recovery through spontaneous phase separation. A high DMC yield (6.5 g·kg·h) over HFIL was achieved under mild conditions compared to non- hydroxyl IL. Self-diffusion coefficients characterization revealed intensified diffusion of CHOH and HFIL, alongside reduced blockage of active sites after hydroxyl functionalization. Density functional theory calculations elucidated that cation polarization induced by hydroxyl group facilitated the synergistic activation of both substrates and monomethyl carbonate intermediate. The reaction mechanism was further verified through diffuse reflectance infrared Fourier transform spectroscopy and theoretical calculations. The self-separation behavior was demonstrated by molecular dynamics simulations. The deep insights into hydroxyl effects towards direct DMC synthesis provide a pioneering perspective for CO capture and utilization using functionalized ILs.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dry reforming of toluene for syngas production over Ni-based perovskite-type oxides 在镍基过氧化物上干法重整甲苯以生产合成气
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-31 DOI: 10.1016/j.apcatb.2024.124555
Jie Ren, Zeeshan Abbasi, Inam Ullah, Feng Zeng
{"title":"Dry reforming of toluene for syngas production over Ni-based perovskite-type oxides","authors":"Jie Ren, Zeeshan Abbasi, Inam Ullah, Feng Zeng","doi":"10.1016/j.apcatb.2024.124555","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124555","url":null,"abstract":"Developing efficient Ni-based catalysts and understanding the mechanism of tar removal are crucial for upgrading biomass gasification technology. Literature has identified the superior performance of Ni-based catalysts in reforming tar model compounds like toluene under a steam atmosphere. In this work, we have synthesized LaCeNiO catalysts and examined their activity with benchmark ABO-type perovskites in dry reforming of toluene (DRT). Catalytic experiments revealed that LaCeNiO catalysts exhibited superior activity and stability regarding toluene conversion (85.4%) compared to LaCeNiO. The structural study, conducted through various techniques, highlighted the easier reducibility of Ni from the ABO perovskite lattice, leaving higher oxygen vacancies, and higher basicity for reactant adsorption in DRT. Besides, DRIFTS experiments confirmed the *CHO-participated pathway of syngas generation from DRT. The findings suggested potential pathways for designing catalysts to support biomass gasification while contributing to global carbon reduction.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhanced low-temperature catalytic activity and stability in methane combustion of Pd−CeO2 nanowires@SiO2 by Pt dispersion 通过铂分散提高 Pd-CeO2 纳米线@SiO2 在甲烷燃烧中的低温催化活性和稳定性
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-30 DOI: 10.1016/j.apcatb.2024.124554
Jinxiong Tao, Hongxia Lin, Jiguang Deng, Yuxi Liu, Lin Jing, Zhiquan Hou, Lu Wei, Zhiwei Wang, Hongxing Dai
{"title":"Enhanced low-temperature catalytic activity and stability in methane combustion of Pd−CeO2 nanowires@SiO2 by Pt dispersion","authors":"Jinxiong Tao, Hongxia Lin, Jiguang Deng, Yuxi Liu, Lin Jing, Zhiquan Hou, Lu Wei, Zhiwei Wang, Hongxing Dai","doi":"10.1016/j.apcatb.2024.124554","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124554","url":null,"abstract":"The long-standing contradiction between low-temperature activity and high-temperature stability is one of the difficulties in catalytic combustion of low-concentration methane. The traditional Pd−CeO catalyst system has been applied to the oxidation of methane with low concentrations. However, the problem of sintering at high temperatures still exists. In this work, we prepared the Pt-modified Pd−CeO nanowires (NW) sample (in which the actual Pt, Pd, and Ce contents were 0.12, 0.86, and 9.8 wt%, respectively) using the one-pot reverse-micelle emulsion method. It was found that Pt-Pd−CeONW@SiO showed the highest low-temperature catalytic activity at a space velocity of 20,000 mL/(g h) and the best water resistance and high-temperature stability in the combustion of methane. The and (the temperatures for achieving methane conversions of 50 and 90 %) were 298 and 342 ℃, respectively, methane reaction rate at 270 ℃ was 0.49 μmol/(g s), and turnover frequency (TOF) at 270 °C was 0.198 s over Pt-Pd−CeONW@SiO; whereas over Pd−CeONW@SiO (in which the actual Pd and Ce contents were 0.82 and 10.6 wt%, respectively), the and were 360 and 420 ℃, respectively, methane reaction rate at 270 ℃ was 0.074 μmol/(g s), and TOF at 270 °C was 0.032 s. The introduction of the highly dispersed Pt to Pd−CeONW@SiO could effectively increase the PdO sites of unsaturated coordination through the electron-donating interaction of the Pt with PdO, which played an important role in activating the C−H bonds in methane. In addition, the unique structure of encapsulation also rendered the Pt-Pd−CeONW@SiO sample to possess good water resistance and thermal stability in methane combustion. We are sure that the present work provides a possibility for developing the catalysts with stable catalytic and water-resistant performance at low and high temperatures in the combustion of methane.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"44 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cerium-optimized platinum-free high-entropy alloy nanoclusters for enhanced ampere-level sustainable hydrogen generation 用于增强安培级可持续制氢的铈优化无铂高熵合金纳米团簇
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-30 DOI: 10.1016/j.apcatb.2024.124529
Yujia Zhang, Kunkun Nie, Binjie Li, Lixin Yi, Chen Hu, Ziyi Wang, Xiaorong Hao, Wenlin Zhang, Zhengqing Liu, Wei Huang
{"title":"Cerium-optimized platinum-free high-entropy alloy nanoclusters for enhanced ampere-level sustainable hydrogen generation","authors":"Yujia Zhang, Kunkun Nie, Binjie Li, Lixin Yi, Chen Hu, Ziyi Wang, Xiaorong Hao, Wenlin Zhang, Zhengqing Liu, Wei Huang","doi":"10.1016/j.apcatb.2024.124529","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124529","url":null,"abstract":"The incorporation of rare earth (RE) elements into high-entropy alloys (HEAs) as electrocatalysts for hydrogen evolution reaction (HER) shows great potential in addressing the energy crisis. Here, we successfully synthesized cerium (Ce)-tailored PdCeMoCuRu HEA with chemical homogeneity and stability using a facile wet-chemical synthesis strategy. The obtained PdCeMoCuRu HEA provides abundant active metal sites, resulting in superior HER performance compared to state-of-the-art Pt/C. It only requires 12.8 mV to achieve a current density of 10 mA cm, which is nearly half that required for Pt/C (24.8 mV). Importantly, it exhibits excellent electrocatalytic durability for 100 hours even under a high current density of 1.0 A cm at the ampere level. Density functional theory (DFT) calculations confirm that the introduction of Ce can modify the electronic configuration and generate synergistic effects around Pd, Cu, and Ru active sites. This work establishes a novel approach for designing efficient RE-tailored HEA electrocatalysts.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Phosphor-doping modulates the d-band center of Fe atoms in Fe-N4 catalytic sites to boost the activity of oxygen reduction 磷掺杂调节了 Fe-N4 催化位点中铁原子的 d 波段中心,从而提高了氧还原的活性
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-30 DOI: 10.1016/j.apcatb.2024.124553
Yuan Qin, Zihao Ou, Chaozhong Guo, Yao Liu, Rong Jin, Chuanlan Xu, Haifeng Chen, Yujun Si, Honglin Li
{"title":"Phosphor-doping modulates the d-band center of Fe atoms in Fe-N4 catalytic sites to boost the activity of oxygen reduction","authors":"Yuan Qin, Zihao Ou, Chaozhong Guo, Yao Liu, Rong Jin, Chuanlan Xu, Haifeng Chen, Yujun Si, Honglin Li","doi":"10.1016/j.apcatb.2024.124553","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124553","url":null,"abstract":"Regulating the electronic structure by phosphor-doping is a preferred strategy to boost the performance of carbon-based catalysts for oxygen reduction reaction (ORR). Here, a porous Fe, P, N-codoped carbon catalyst (PCF-FeTz-900) is designed by a phytic acid-assisted thermal etching strategy, in which P atoms are first doped into the carbon matrix to form a stable PC bond, and then FeN sites are produced from Fe-2,4,6-Tris(2-pyridyl)-s-triazine complex (Fe-TPTz). Theoretical calculations suggest that the electrons are transferred from the doped P atom to the neighboring FeN sites, which facilitates the ORR at the Fe sites by reducing the energy barrier and the adsorption energy of intermediates. Additionally, the P-doped FeN (FeNP) structure manifests a lower free energy difference than that of FeN and the -band center of Fe is also lowered, which further ensures its higher ORR catalytic ability. As a result, the PCF-FeTz-900 catalyst exhibits superior ORR activity and stability in alkaline electrolyte, and the assembled primary zinc-air battery shows greater performances compared to the commercial Pt/C catalyst. This work can provide an effective pathway for modulating the performance of doped-carbon materials in energy conversion devices.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"61 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205114","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ultra-low temperature selective catalytic reduction of NOx into N2 by micron spherical CeMnOx in high-humidity atmospheres containing SO2 在含有二氧化硫的高湿度大气中,微米球形氧化锰通过超低温选择性催化将氮氧化物还原为 N2
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-30 DOI: 10.1016/j.apcatb.2024.124552
Xixi Chen, Peng Gao, Ling Huang, Yongji Hu, Jianhai Wang, Zonghang Liu, Yuesong Shen
{"title":"Ultra-low temperature selective catalytic reduction of NOx into N2 by micron spherical CeMnOx in high-humidity atmospheres containing SO2","authors":"Xixi Chen, Peng Gao, Ling Huang, Yongji Hu, Jianhai Wang, Zonghang Liu, Yuesong Shen","doi":"10.1016/j.apcatb.2024.124552","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124552","url":null,"abstract":"The solvothermal synthesis of optimized micron-sized spherical CeMnO-350 yields remarkable results in ultra-low temperature NH-SCR of NO, with over 91 % NO conversion achieved between 59 and 255 ℃. Notably, under 5 vol% HO and 50 ppm SO, the CeMnO maintains NO conversion >99 % at 127 ℃ for extended periods, surpassing current ultra-low temperature deNO standards. This superior performance is attributed to the material's unique characteristics: the regular and porous surface morphology enhances exposure to active sites, particularly MnO(112) facets crucial for ultra-low temperature deNO, while the rough and loose surface and high MnO(222) exposure mitigate water vapor and SO poisoning. Furthermore, the thermal storage effect of the MnO/MnO system within CeMnO facilitates rapid thermal dissipation and ammonium sulfite decomposition. This process is further augmented by the pores, which aid in the confinement of deNO reaction heat and facilitate the flushing of flowing flue gas, thereby impeding the formation of ammonium bisulfate.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"44 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Wood-derived continuously oriented channels coupled with tunable built-in electric fields for efficient oxygen evolution 木质连续定向通道与可调内置电场相结合,实现高效氧气进化
Applied Catalysis B: Environment and Energy Pub Date : 2024-08-28 DOI: 10.1016/j.apcatb.2024.124550
Luosong Zheng, Heping Luo, Yuxin Zhong, Wanqian Li, Han Xu, Fuquan Xiong, Jiahao Pi, Yan Qing, Yiqiang Wu
{"title":"Wood-derived continuously oriented channels coupled with tunable built-in electric fields for efficient oxygen evolution","authors":"Luosong Zheng, Heping Luo, Yuxin Zhong, Wanqian Li, Han Xu, Fuquan Xiong, Jiahao Pi, Yan Qing, Yiqiang Wu","doi":"10.1016/j.apcatb.2024.124550","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124550","url":null,"abstract":"Interface engineering has emerged as a promising strategy for efficiently enhancing catalytic performance. Herein, we present a built-in electric field (BEF) strategy to assemble CoS/NiS heterojunctions confined in S-doped carbon matrix (SC) and anchored S-doped carbide wood framework (SCW). Leveraging BEF, Co-S-Ni charge transfer channels and the superior mass transfer properties inherent in wood’s unique structure, (CoS/NiS)@SC/SCW exhibits a low overpotential of 220 mV at 50 mA cm, and remarkable stability. The experimental characterizations and theoretical simulation indicate that the constructed BEF can induce the directional transfer of electrons from CoS to NiS, which is beneficial for the adsorption of OH owing to the electrostatic interaction, thereby promotes the formation of the highly active amorphous metal hydroxide oxides at lower OER potentials. This work provides a new perspective for exploring the design of energy storage and conversion catalysts based on renewable wood substrates.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226218","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","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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