机构地区:[1]Key Laboratory for Advanced Materials,Shanghai Engineering Research Center for Multi–media Environmental Catalysis and Resource Utilization,Joint International Research Laboratory of Precision Chemistry and Molecular Engineering,Feringa Nobel Prize Scientist Joint Research Center,School of Chemistry and Molecular Engineering,East China University of Science&Technology,Shanghai 200237,China [2]National Engineering Research Center of Industrial Wastewater Detoxication and Resource Recovery,State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process,East China University of Science and Technology,Shanghai 200237,China [3]State Key Laboratory of Urban Water Resource and Environment,Harbin Institute of Technology,Harbin 150090,Heilongjiang,China [4]Shanghai Institute of Pollution Control and Ecological Security,Shanghai 200092,China [5]Institute of Materials Research,Tsinghua Shenzhen International Graduate School,Tsinghua University,Shenzhen 518055,Guangdong,China [6]COMSATS Univ Islamabad,Interdisciplinary Res Ctr Biomed Mat IRCBM,Lahore Campus,Lahore 54000,Pakistan
出 处:《Chinese Journal of Catalysis》2025年第4期234-245,共12页催化学报(英文)
基 金:国家重点研发项目(2022YFB3803600,2022YFE0107900);国家自然科学基金(22476050,21972040);上海市教委创新计划(2021-01-07-00-02-E00106);上海市科学技术委员会(22230780200,20DZ2250400);中央高校基本科研业务费(222201717003);城市水资源与水环境国家重点实验室开放课题(QA202319);上海市教委晨光项目(23CGA40).
摘 要:Developing efficient photocatalysts to address collaborative energy and environmental crises still faces significant challenges.In this report,we present a highly efficient MXene–based photocatalyst,which is combined with MoS_(2)nano patches and TiO_(2)/Ti_(3)C_(2)(TTC)nanowires through hydrothermal treatment.Of all the composites tested,the optimized photocatalyst gave a remarkable H_(2)and revolving polylactic acid(PLA)into pyruvic acid(PA).Achieving a remarkable H_(2)evolution rate of 637.1 and 243.2μmol g^(−1)h^(−1),in the presence of TEOA and PLA as a sacrificial reagent under UV-vis(λ≥365 nm)light irradiation.The improved photocatalytic activity is a result of the combination of dual cocatalyst on the surface of TTC photocatalyst,which create an ideal synergistic effect for the generation of PA and the production of H_(2)simultaneously.The MoS_(2)TiO_(2)/Ti_(3)C_(2)(MTT)composite can generate more photoexcited charge carriers,leading to the generation of more active radicals,which may enhance the system's photocatalytic activity.This work aims at demonstrating its future significance and guide the scientific community towards a more efficient approach to commercializing H_(2)through photocatalysis.聚乳酸(PLA)作为一种可降解塑料,已被广泛应用于市场.光催化技术作为一种绿色、可持续的处理方法,在PLA资源化转化方面展现出显著潜力.尽管前期研究主要集中在光催化产氢和增值化合物的合成上以应对能源和环境危机.当前研究趋势正转向通过光重整技术实现塑料氧化过程调控,不仅解决有害化合物污染问题,并生成绿色能源.该反应的关键在于有序地打破乳酸中的C–OH和C–H键,构健PLA到丙酮酸(PA)的高选择性回收路径.因此,设计高性能的光催化剂,成为实现PLA向PA高选择性定向转化的关键科学挑战.本文设计了一种高效的MoS_(2)/TiO_(2)/Ti_(3)C_(2)纳米线光催化系统,在紫外-可见光照射下,实现了PLA的氧化转化并生成氢气.首先,Ti_(3)C_(2)纳米片被转化为TiO_(2)/Ti_(3)C_(2)(TTC)纳米线复合材料,随后通过水热过程将MoS_(2)均匀负载在TTC复合材料表面,产生协同效应以提高光催化剂的活性.在光催化产氢测试中,以三乙醇胺作为牺牲试剂,获得的最高的氢气产生速率为637.1μmol g^(–1)h^(–1),是TTC纳米线的7.1倍.进一步拓展该体系至PLA转化体系,使用预处理的PLA溶液作为牺牲试剂时,氢气产生速率为243.2μmol g^(–1)h^(–1),并同步实现了PLA向PA的选择性氧化转化.Ti_(3)C_(2)和MoS_(2)的结合形成了有效的复合材料,因双助催化剂的协同效应而增强了光催化活性.将MoS_(2)加入TTC光催化剂中,提高了氢气生成的特定活性(请重新梳理此句表达).PLA塑料在光照下解聚为乳酸,乳酸通过空穴氧化为丙酮酸离子,这些丙酮酸离子进一步转化为PA,最终实现了PLA塑料直接光重整和氢气生成.综上,本文以原位生成和后负载两种方式制备了双助光催化剂,在光照下同步实现了废弃塑料的资源化与产氢,极大地提高了光催化技术经济价值,为后续相关高价值体系的开发和应用提供参考.
关 键 词:Photo reforming Polylactic acid Hydrogen evolution Lactic acid Pyruvic acid
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