{"title":"Efficient photocatalytic H2O2 production and green oxidation of glycerol over a SrCoO3-incorporated catalyst","authors":"Yuxuan He, Yongming Wang, Jin Qian, Kailin Xu, Bianhe Lu, Sijing Tang, Yin Liu, Junwei Shen","doi":"10.1016/j.apcatb.2024.124565","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124565","url":null,"abstract":"Photocatalysis for HO production suffers from low carrier utilization and slow reaction kinetics. Herein, a photocatalytic system supported by a SrCoO-MoS (SCOS) heterojunction, which possessed a unique S-O electron transport channel, was proposed to facilitate HO production under condition where glycerol served as a sacrificial agent. The SCOS heterojunction achieved a remarkable yield of 15.90 mmol g h HO production, 3.7 times higher than the base component SCO. The construction of the heterojunction enriched the oxygen vacancies on the catalyst surface, facilitated photogenerated charge separation, and promoted the adsorption of O, reducing the oxygen reduction reaction (ORR) energy barrier. Besides, glycerol served as a unique proton donor, efficiently captured holes to enhance HO production, and generated valuable by-products including glyceric acid and dihydroxyacetone. Furthermore, SCOS exhibited excellent stability over repeated cycles with consistent HO yields. This study offers an efficient photocatalytic system and demonstrates glycerol’s potential in green oxidation processes.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"29 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142249999","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}
Yi Zhao, He Cui, Yidong Hu, Shunli Li, Feng Liu, Boxiong Shen, Kai Ge, Binyuan Liu, Yongfang Yang
{"title":"A two dimensional hierarchically porous MOF-Cu with large lateral size via amino-groups regulated hydrolysis strategy and its superior photocatalytic reduction of CO2","authors":"Yi Zhao, He Cui, Yidong Hu, Shunli Li, Feng Liu, Boxiong Shen, Kai Ge, Binyuan Liu, Yongfang Yang","doi":"10.1016/j.apcatb.2024.124567","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124567","url":null,"abstract":"A two-dimensional hierarchically porous (2D HP) MOF-Cu layer with a large lateral size was prepared by the amino-groups regulated hydrolysis strategy. The resultant large 2D MOF-Cu layer has many defects owing to the replacement of partial ligands via -OH. 2D HP MOF-Cu large layer showed significantly enhanced photocatalytic activity under full-spectrum irradiation (with the CO production rate about 4.4 times that of the original 3D MOF-Cu sheets). DFT results confirmed that the defective 2D HP MOF-Cu large layer exhibited the new defective state in the valence band, which narrowed the band gap, broadened the light absorption range, promoted the electron transfer, and decreased the Gibbs free energy barrier for COOH* → CO* (about 0.61 eV). This work provides a facile method for the preparation of the defective 2D HP MOFs large layers via the regulation of amino groups from the organic ligands and elucidates the mechanism for improved photocatalytic efficiency.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"33 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226214","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}
Yifei Wang, Yan Du, Peiyang Duan, Beibei Li, Junshan Li, Yongfa Zhu
{"title":"Asymmetrical facet-oriented anisotropic charge migration of MIL-101(Fe) with internal electric field-steered photogenerated holes for boosting photocatalytic oxidation","authors":"Yifei Wang, Yan Du, Peiyang Duan, Beibei Li, Junshan Li, Yongfa Zhu","doi":"10.1016/j.apcatb.2024.124564","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124564","url":null,"abstract":"Controllably steering the photogenerated charge behaviors of semiconductor photocatalysts is crucial in improving photocatalytic oxidation. By engineering the primary facet from (101) to (112), the asymmetrical feather of MIL-101(Fe)(112) result in potential difference on varied facets to contribute to anisotropic charge migration, which has been determined by the preferentially photodeposited cocatalysts on facet (112) and facet (119) of the nanocrystal. Thus-observed anisotropic charge migration of MIL-101(Fe)(112) contribute to 10 times stronger internal electric field (IEF) to accelerate charge separation and migration. Also, we demonstrate the lowest unoccupied crystal orbital (LUCO) of MIL-101(Fe)(112) deepened (up to 3.33 eV vs. NHE) and acquire 3.5 times higher photogenerated holes for robust hole oxidation capacities. As a proof-of-concept, the optimal MIL-101(Fe)(112) can acquire 100 % higher degradation rate and 33 % higher mineralization than MIL-101(Fe)(101). This work highlights the importance of unsymmetric facet manipulation in tailoring photocatalysts for efficient photocatalytic oxidation.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205081","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}
{"title":"Selective electrosynthesis of ammonia via nitric oxide electroreduction catalyzed by copper nanowires infused in nitrogen-doped carbon nanorods","authors":"Dinesh Dhanabal, Yuyeon Song, Seoyoung Jang, Sangaraju Shanmugam","doi":"10.1016/j.apcatb.2024.124577","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124577","url":null,"abstract":"The electrochemical nitric oxide reduction reaction (eNORR) is meticulously investigated as an alternative to the energy intensive Haber-Bosch process to produce Ammonia (NH). However, the eNORR is hindered by NH selectivity due to side reactions and mass-transfer limitations. In this work, we rationally designed copper nanowires (Cu NWs) infused in the lotus-root-like multi-nano-channels of the porous N-doped carbon nanorods (Cu-mNCNR) for a high selective eNORR to synthesize NH at ambient conditions. The optimized catalyst, Cu-mNCNR2, has achieved the highest NH Faradaic efficiency of 79% with NH yield rate of 34.5 μmol cm h at −0.4 V. Moreover, the Cu-mNCNR2 has demonstrated a vigorous performance in the 24 h continuous NO electrolysis to produce NH. Additionally, a prototype device, the Zn-NO battery, was demonstrated. This study shows that the rational design of a catalyst considering mass-transfer limitations is crucial to achieving high selective NH electrosynthesis in eNORR.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"4 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142250000","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}
{"title":"A highly active and stable Pd/15CoAlOx catalyst with Pd-Co composite interfaces for methane combustion","authors":"Jieying Cai, Shenghai Wu, Miaomiao Liu, Yan Zhang, Meng Wang, Yun Liu, Yunbo Yu, Wenpo Shan","doi":"10.1016/j.apcatb.2024.124559","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124559","url":null,"abstract":"A series of Pd/yCoAlO (where y represents the Co/AlO mass ratio, ranging from 0 to 20.0 wt%) catalysts for CH combustion were synthesized, among which the Pd/15CoAlO catalyst exhibited excellent activity, stability and water resistance. HRTEM, XRD, and Raman results indicated that the Pd/15CoAlO catalyst comprised two phases, namely CoAlO and CoO. H-TPR, O-TPD, and in-situ DRIFTS revealed that Pd/15CoAlO featuring Pd-Co composite interfaces strengthened the anchoring of PdO and facilitated electron transfer between Pd-Co interfaces. Moreover, active oxygen species were enriched at the interface, which promoted the reaction pathway involving the change from methoxy to formate, rather than from methyl to formate. Multiple characterizations and analyses indicated that Pd/15CoAlO exhibited a MSI weaker than the Pd-CoO interface but stronger than that observed at the Pd-AlO interface. The appropriate level of interaction avoided the excessive oxidation of Pd, ensuring the presence of a substantial quantity of unsaturated Pd sites.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"95 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205116","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}
Muhammad Ajmal, Shishi Zhang, Xiaolei Guo, Xiaokang Liu, Chengxiang Shi, Ruijie Gao, Zhen-Feng Huang, Lun Pan, Xiangwen Zhang, Ji-Jun Zou
{"title":"Rapid reconstruction of nickel iron hydrogen cyanamide with in-situ produced proton acceptor for efficient oxygen evolution","authors":"Muhammad Ajmal, Shishi Zhang, Xiaolei Guo, Xiaokang Liu, Chengxiang Shi, Ruijie Gao, Zhen-Feng Huang, Lun Pan, Xiangwen Zhang, Ji-Jun Zou","doi":"10.1016/j.apcatb.2024.124561","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124561","url":null,"abstract":"Metal oxyhydroxide (MOOH) through irreversible reconstructed fabrication from transition metal compounds are highly efficient oxygen evolution reaction (OER) electrocatalysts but face limits from adsorption energy scaling relationship and sluggish deprotonation kinetics. Herein, we present Fe-doped nickel hydrogen cyanamide (NiFe-HC), which is rapidly surface reconstructed into NiFe(OOH)-HC after OER. In-situ Raman spectroscopy and density functional theory (DFT) calculations, revealed that under OER conditions, -HNCN- converts into -NCN- ligand incorporating its abundant and uniform distribution across the active sites. DFT calculations further indicate that Fe predominantly acts as the active site, with -NCN- ligands contribute to the OER by facilitating the deprotonation of *OH in the rate-determining step (RDS), acting effectively as proton acceptor. The ensemble effect between Fe and -NCN- ligand forms the foundation of the exceptional electrocatalytic performance of NiFe(OOH)-HC (190 mV at 20 mA·cm). This discovery offers insights for designing innovative MOOH pre-catalysts to enhance OER efficiency.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"199 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142250050","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}
Zhiqiang Zhang, Yu Le, Lei Jing, Gongxun Huang, Jincan Kang, Qinghong Zhang, Ye Wang
{"title":"Foam-structured Fe catalysts for enhanced heat and mass transfer in synthesis of olefins from syngas","authors":"Zhiqiang Zhang, Yu Le, Lei Jing, Gongxun Huang, Jincan Kang, Qinghong Zhang, Ye Wang","doi":"10.1016/j.apcatb.2024.124569","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124569","url":null,"abstract":"The Fischer-Tropsch (FT) synthesis, characterized by its highly exothermic and high-throughput nature, traditionally yields a mix of C hydrocarbons and C1 by-products, which adversely affect carbon utilization efficiency. Herein, we design a Fe-foam structured catalyst to selectively produce high-value olefins in FT process. The Na-Zn-Fe/Fe-foam catalysts are prepared through a hydrothermal synthesis method, where the FeCO precursor is formed from Fe-foam, followed by addition of sodium and zinc modifiers. These catalysts achieve a remarkable olefin selectivity of ∼80 % and a space-time yield of ∼0.70 g g h at a CO conversion of 98 %, and further demonstrate outstanding stability. The structured catalysts, with expansive void volume and fully open network architecture, provide superior mass and heat transfer capabilities, and effectively mitigate the generation of CO and CH, offering a significant advantage in FT synthesis. This work presents a new strategy for the development of efficient catalysts in high exothermic catalytic reactions.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205088","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}
{"title":"The electron shuttle of aloe-emodin promotes the Cu-FeOOH solid solution photocatalytic membrane to activate hydrogen peroxide for the degradation of tannic in traditional Chinese medicine wastewater","authors":"Mengzhen Zhu, Jiajia Li, Manhua Chen, Yulu Liu, Qiong Mei, Hongbo Liu, Yuping Tang, Qizhao Wang","doi":"10.1016/j.apcatb.2024.124566","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124566","url":null,"abstract":"The inactive macromolecular substances would result in the membrane fouling and reduce the membrane flux in treating traditional Chinese medicine wastewater. Here, we report a novel photocatalytic membrane and utilize aloe-emodin (AE) as electron shuttle synergistically doped into Cu-FeOOH solid solution, then support the photocatalyst AE/Cu-FeOOH on PVDF membrane, which can effectively degrade tannic (95.69 %, 60 min). Furthermore, even after 6 hours of tannic solution filtration, the membrane maintains a high flux of 517 L m h bar. Combined with various spectral and photoelectric performance tests confirmed that AE/Cu-FeOOH-PVDF possesses high separation and transfer efficiency of photogenerated carriers. Meanwhile DFT calculation showed that the composite has better adsorption properties and HO activation ability. AE provided e to Cu-FeOOH, which accelerated the redox reaction process of Fe and Cu ions and produced more stable active free radicals to degrade tannic. This study provides a more environmentally friendly approach for utilizing photocatalytic membranes in the treatment of traditional Chinese medicine wastewater.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"14 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205085","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}
{"title":"Synergistically flexible-robust effects mediate the dynamic reconfiguration of perylene diimide polymer to enhance piezo-photocatalytic nitrate reduction","authors":"Jiwen Zhang, Kailong Lv, Jinke Cheng, Yuhui Liu, Yi Wang, Shuang-Feng Yin, Peng Chen","doi":"10.1016/j.apcatb.2024.124558","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124558","url":null,"abstract":"Identifying the spatial dynamic reconstruction of π-conjugated polymers for efficient carrier transport and controlling the intermediate process of the reaction are urgent and formidable challenges. In this study, a fresh perspective has emerged proposing to synergistically enhance the adaptability and resilience of dynamic torsion patterns in π-conjugated polymers to mediate charge separation and molecular activation. Excitingly, the highest flexible-robust structure and polarity of naphthalene-linked perylene diimide polymer (N-PDA) demonstrates a highest nitrate reduction rate of 5.36 mmol g h under light irradiation and ultrasonic condition, which is 7.5 times that of H-PDA. Theoretical calculations and experimental observations indicate that the strongest flexible-robust structure of N-PDA enhances the inclination of the rigid plane and atomic bond length, resulting in an accelerated uneven distribution of charges, molecular polarity, and electronic coupling to facilitate charge separation dynamics. Moreover, it exposes active sites that promote the adsorption and activation of NO ions while simultaneously regulating intermediate hydrogenation processes. Our study offers innovative prospects for enhancing catalytic efficiency through the implementation of spatial steric configuration of π-conjugated polymers.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"29 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142205086","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}
Kai Wang, Chuang Liu, Jingping Li, Qiang Cheng, Bin Liu, Jun Li
{"title":"Near-infrared-responsive sea-urchin-like Ag6Si2O7/Bi19Br3S27 S-scheme heterojunction for efficient CO2 photoreduction","authors":"Kai Wang, Chuang Liu, Jingping Li, Qiang Cheng, Bin Liu, Jun Li","doi":"10.1016/j.apcatb.2024.124560","DOIUrl":"https://doi.org/10.1016/j.apcatb.2024.124560","url":null,"abstract":"The construction of S-scheme heterojunctions effectively facilitates the spatial separation of photogenerated charge carriers for their involvement in photoreactions. However, the inefficient utilization of solar energy in these heterostructures is often due to unfavorable band-edge positions and suboptimal charge transport dynamics, which result in low photocatalytic efficiency when considering kinetic factors. In this study, sea urchin–like BiBrS/AgSiO S-scheme heterojunctions are fabricated, which exhibit excellent CO photoreduction performance under ultraviolet, visible, and near-infrared (NIR) light illumination. Experimental data and density functional theory calculations confirm the S-scheme charge transfer mechanisms, which enable the efficient separation of photogenerated carriers for CO reduction. Consequently, the optimized AgSiO/BiBrS heterostructures exhibit superior CO photoreduction activity under NIR light irradiation. This approach offers a strategy for designing advanced NIR-light-responsive photocatalysts for efficient CO photoreduction.","PeriodicalId":516528,"journal":{"name":"Applied Catalysis B: Environment and Energy","volume":"11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142226215","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}