Ferroelectric polarization enabled spatially selective adsorption of redox mediators to promote Z-scheme photocatalytic overall water splitting
文献类型:期刊论文
作者 | Kang, Yuyang1; Qi, Haozhi1,2; Wan, Gedeng1,2; Zhen, Chao1; Xu, Xiaoxiang3; Yin, Li-Chang1; Wang, Lianzhou4,5; Liu, Gang1,2; Cheng, Hui-Ming1,6 |
刊名 | JOULE |
出版日期 | 2022-08-17 |
卷号 | 6期号:8页码:1876-1886 |
ISSN号 | 2542-4351 |
DOI | 10.1016/j.joule.2022.06.017 |
通讯作者 | Liu, Gang(gangliu@imr.ac.cn) |
英文摘要 | Although the artificial Z-scheme system, mimicking natural photosyn-thesis, has shown promising applications in photocatalytic water split-ting, it often suffers from the side reaction of redox mediator, which considerably undermines the efficacy of photocarrier utilizations. Herein, we propose to suppress the side reaction by using ferroelec-tric polarization, which not only provides a strong driving force to spatially separate photocarriers to the oppositely poled surface but also induces spatially selective adsorption of redox ions. Single -domain ferroelectric PbTiO3 nanoplates have been adopted as a model ferroelectric to construct the Z-scheme system with BiVO4 par-ticles and a cationic redox mediator. In contrast to the inactive multi -domain ferroelectric PbTiO3-based system, the so-formed Z-scheme system delivers stable high activity for photocatalytic overall water splitting under both visible light and simulated solar insolation. This work offers a proof of concept to realize efficient solar photocatalytic water splitting based on single-domain ferroelectric Z-scheme system. |
资助项目 | National Key R&D Program of China[2021YFA1500800] ; National Natural Science Foundation of China[52002377] ; National Natural Science Foundation of China[51825204] ; National Natural Science Foundation of China[52120105003] ; National Natural Science Foundation of China[52188101] ; China Postdoctoral Sci- ence Foundation[2020M681003] ; China Postdoctoral Sci- ence Foundation[2020TQ0327] ; China Postdoctoral Sci- ence Foundation[2020BS009] ; China Postdoctoral Science Foundation[2020TQ0327] ; China Postdoctoral Science Foundation[2020BS009] ; Natural Science Foundation of Liaoning Province[2020M681003] ; CAS Projects for Young Scientists in Basic Research[2020TQ0327] ; [YSBR-004] |
WOS研究方向 | Chemistry ; Energy & Fuels ; Materials Science |
语种 | 英语 |
出版者 | CELL PRESS |
WOS记录号 | WOS:000861328000014 |
资助机构 | National Key R&D Program of China ; National Natural Science Foundation of China ; China Postdoctoral Sci- ence Foundation ; China Postdoctoral Science Foundation ; Natural Science Foundation of Liaoning Province ; CAS Projects for Young Scientists in Basic Research |
源URL | [http://ir.imr.ac.cn/handle/321006/175609] |
专题 | 金属研究所_中国科学院金属研究所 |
通讯作者 | Liu, Gang |
作者单位 | 1.Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China 2.Univ Sci & Technol China, Sch Mat Sci & Engn, 72 Wenhua Rd, Shenyang 110016, Peoples R China 3.Tongji Univ, Sch Chem Sci & Engn, Shanghai Key Lab Chem Assessment & Sustainabil, 1239 Siping Rd, Shanghai 200092, Peoples R China 4.Univ Queensland, Nanomat Ctr, Sch Chem Engn, Brisbane, Qld 4072, Australia 5.Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia 6.Chinese Acad Sci, Inst Technol Carbon Neutral, Shenzhen Inst Adv Technol, 1068 Xueyuan Blvd, Shenzhen 518055, Peoples R China |
推荐引用方式 GB/T 7714 | Kang, Yuyang,Qi, Haozhi,Wan, Gedeng,et al. Ferroelectric polarization enabled spatially selective adsorption of redox mediators to promote Z-scheme photocatalytic overall water splitting[J]. JOULE,2022,6(8):1876-1886. |
APA | Kang, Yuyang.,Qi, Haozhi.,Wan, Gedeng.,Zhen, Chao.,Xu, Xiaoxiang.,...&Cheng, Hui-Ming.(2022).Ferroelectric polarization enabled spatially selective adsorption of redox mediators to promote Z-scheme photocatalytic overall water splitting.JOULE,6(8),1876-1886. |
MLA | Kang, Yuyang,et al."Ferroelectric polarization enabled spatially selective adsorption of redox mediators to promote Z-scheme photocatalytic overall water splitting".JOULE 6.8(2022):1876-1886. |
入库方式: OAI收割
来源:金属研究所
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