机构地区:[1]Key Laboratory of the Ministry of Education for Advanced Catalysis Materials,College of Chemistry and Materials Science,Zhejiang Normal University,Jinhua 321004,China [2]College of Biological,Chemical Sciences and Engineering and Nanotechnology Research Institute,Jiaxing University,Jiaxing 314001,China [3]College of Geography and Environmental Sciences,Zhejiang Normal University,Jinhua 321004,China [4]College of Chemical and Biological Engineering,Zhejiang University,Hangzhou 310058,China [5]School of Biological and Chemical Engineering,Panzhihua University,Panzhihua 617000,China
出 处:《Nano Research》2024年第6期5022-5030,共9页纳米研究(英文版)
基 金:the National Natural Science Foundation of China(No.21603191);Zhejiang Provincial Natural Science Foundation of China(Nos.LY20B030003 and LQ16B010001);Public Welfare Technology Application Research Plan Project of Zhejiang Province(Analysis Test Item,No.2017C37024);Foundation of Science and Technology Bureau of Jinhua(No.20204185),;Self-Topic Fund of Zhejiang Normal University(No.2020ZS04).
摘 要:Selective loading of spatially separated redox cocatalysts on direct Z-scheme heterojunctions holds great promise for advancing the efficiency of artificial photosynthesis,which however is limited to the photodeposition of noble metal cocatalysts and the fabrication of hollow double-shelled semiconductor heterojunctions.Moreover,the co-exposure of discrete cocatalyst and semiconductor increases the product diversity when both the exposed sites of which participate in CO_(2)photoreduction.Herein,we present a facile and versatile protocol to overcome these limitations via surface coating of Z-scheme heterojunctions with bifunctional noble-metal-free cocatalysts.With Cu_(2)O/Fe_(2)O_(3)(CF)as a model heterojunction and layered Ni(OH)_(2)as a model cocatalyst,it is found that Ni(OH)_(2)lying on the surfaces of Cu_(2)O and Fe_(2)O_(3)separately co-catalyzes the CO_(2)reduction and H_(2)O oxidation.Thorough experimental and theoretical investigation reveals that the Ni(OH)_(2)outer layer:(i)mitigates the charge recombination in CF and balances their transfer and consumption;(ii)reduces the rate-determining barriers for CO_(2)-to-CO and H_(2)O-to-O_(2)conversion,(iii)suppresses the side proton reduction occurring on CF,and(iv)protects the CF from component detachment.As expected,the redox reactions stoichiometrically proceed,and significantly enhanced photocatalytic activity,selectivity,and stability in CO generation are achieved by the stacked Cu_(2)O/Fe_(2)O_(3)@Ni(OH)_(2)in contrast to CF.This study demonstrates the significance of the synergy between bifunctional cocatalysts and Z-scheme heterojunctions for improving the efficacy of overall redox reactions,opening a fresh avenue for the rational design of artificial photosynthetic systems.
关 键 词:Z-scheme heterojunction bifunctional cocatalyst CO_(2)reduction H_(2)O oxidation stoichiometric redox reaction
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