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作 者:Kai Song Fang He Ergang Zhou Lin Wang Huilin Hou Weiyou Yang
机构地区:[1]School of Materials Science and Engineering,Tianjin University,Tianjin 300350,China [2]Tianjin Key Laboratory of Composite and Functional Materials,Tianjin University,Tianjin 300350,China [3]Institute of Micro/Nano Materials and Devices,Ningbo University of Technology,Ningbo 315211,Zhejiang,China
出 处:《Journal of Energy Chemistry》2022年第5期49-59,共11页能源化学(英文版)
基 金:supported by the project funded by the National Natural Science Foundation of China (52172222, 5197226 and 51972178);the China Postdoctoral Science Foundation(2020 M681966);the exchange project of the sixth ChinaNorthern Macedonia Science and Technology Meeting (6-11);the Natural Science Foundation of Ningbo Municipal Government(202003 N4164 and 2021J145)。
摘 要:The sluggish kinetics for water oxidation is recognized as one of the major problems for the unsatisfied photoelectrochemical(PEC) performance. Herein, we developed a feasible strategy based on in-situ selective surface cation exchange, for activating surface water oxidation reactivity toward boosted PEC water oxidation of BiVO_(4) photoanodes with fundamentally improved surface charge transfer. The asconstructed Co/BiVO_(4) photoanodes exhibit 2.6 times increase in photocurrent density with superior stability, in comparison to those of pristine counterpart. Moreover, the faradaic efficiency of as-fabricated photoanode can be up to ~ 95% at 1.23 V(vs. RHE). The unique selective replacement of Bi by Co on the surface could modify the electronic structure of BiVO_(4) with reduced energy barrier of the deprotonation of OH^(+) to O, thus favoring the overall excellent PEC performance of Co/BiVO_(4) photoanode.
关 键 词:Cation exchange BIVO4 PHOTOELECTROCHEMICAL Water oxidation
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