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用于太阳能水氧化的具有类珍珠层催化多层结构的赤铁矿界面工程

Interface Engineering of Hematite with Nacre-like Catalytic Multilayers for Solar Water Oxidation.

作者信息

Choi Yeongkyu, Jeon Dasom, Choi Yuri, Kim Dongseok, Kim Nayeong, Gu Minsu, Bae Sanghyun, Lee Taemin, Lee Hyun-Wook, Kim Byeong-Su, Ryu Jungki

机构信息

Department of Chemistry, School of Natural Science , Ulsan National Institute of Science and Technology (UNIST) , Ulsan 44919 , Republic of Korea.

Department of Energy Engineering, School of Energy and Chemical Engineering , Ulsan National Institute of Science and Technology (UNIST) , Ulsan 44919 , Republic of Korea.

出版信息

ACS Nano. 2019 Jan 22;13(1):467-475. doi: 10.1021/acsnano.8b06848. Epub 2018 Dec 6.

DOI:10.1021/acsnano.8b06848
PMID:30512922
Abstract

An efficient water oxidation photoanode based on hematite has been designed and fabricated by tailored assembly of graphene oxide (GO) nanosheets and cobalt polyoxometalate (Co-POM) water oxidation catalysts into a nacre-like multilayer architecture on a hematite photoanode. The deposition of catalytic multilayers provides a high photocatalytic efficiency and photoelectrochemical stability to underlying hematite photoanodes. Compared to the bare counterpart, the catalytic multilayer electrode exhibits a significantly higher photocurrent density and large cathodic shift in onset potential (∼369 mV) even at neutral pH conditions due to the improved charge transport and catalytic efficiency from the rational and precise assembly of GO and Co-POM. Unexpectedly, the polymeric base layer deposited prior to the catalytic multilayers improves the performance even more by facilitating the transfer of photogenerated holes for water oxidation through modification of the flat band potential of the underlying photoelectrode. This approach utilizing polymeric base and catalytic multilayers provides an insight into the design of highly efficient photoelectrodes and devices for artificial photosynthesis.

摘要

通过将氧化石墨烯(GO)纳米片和钴多金属氧酸盐(Co-POM)水氧化催化剂定制组装成赤铁矿光阳极上类似珍珠母的多层结构,设计并制造了一种基于赤铁矿的高效水氧化光阳极。催化多层膜的沉积为下层的赤铁矿光阳极提供了高光催化效率和光电化学稳定性。与未修饰的对应物相比,催化多层电极即使在中性pH条件下也表现出显著更高的光电流密度和起始电位的大幅阴极偏移(约369 mV),这归因于GO和Co-POM的合理精确组装提高了电荷传输和催化效率。出乎意料的是,在催化多层膜之前沉积的聚合物基层通过改变下层光电极的平带电位促进光生空穴向水氧化的转移,进一步提高了性能。这种利用聚合物基层和催化多层膜的方法为人工光合作用高效光电极和器件的设计提供了思路。

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