A red-light-powered silicon nanowire biophotochemical diode for simultaneous CO2 reduction and glycerol valorization

IF 42.8 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jimin Kim, Jia-An Lin, Jinhyun Kim, Inwhan Roh, Soohyung Lee, Peidong Yang
{"title":"A red-light-powered silicon nanowire biophotochemical diode for simultaneous CO2 reduction and glycerol valorization","authors":"Jimin Kim, Jia-An Lin, Jinhyun Kim, Inwhan Roh, Soohyung Lee, Peidong Yang","doi":"10.1038/s41929-024-01198-1","DOIUrl":null,"url":null,"abstract":"A bias-free photochemical diode, in which a p-type photocathode is connected to an n-type photoanode to harness light for driving photoelectrochemical reduction and oxidation pairs, serves as a platform for realizing light-driven fuel generation from CO2. However, the conventional design, in which cathodic CO2 reduction is coupled with the anodic oxygen evolution reaction (OER), requires substantial energy input. Here we present a photochemical diode device that harnesses red light (740 nm) to simultaneously drive biophotocathodic CO2-to-multicarbon conversion and photoanodic glycerol oxidation as an alternative to the OER to overcome the above thermodynamic limitation. The device consists of an efficient CO2-fixing microorganism, Sporomusa ovata, interfaced with a silicon nanowire photocathode and a Pt–Au-loaded silicon nanowire photoanode. This photochemical diode operates bias-free under low-intensity (20 mW cm−2) red light irradiation with ~80% Faradaic efficiency for both the cathodic and anodic products. This work provides an alternative photosynthetic route to mitigate excessive CO2 emissions and efficiently generate value-added chemicals from CO2 and glycerol. CO2 reduction to value-added products is an attractive strategy in sustainable chemistry. Now a photochemical diode simultaneously drives biophotocathodic CO2-to-multicarbon conversion and photoanodic glycerol oxidation under red light with a photocurrent density of ~1.2 mA cm−2 and a Faradaic efficiency of ~80%.","PeriodicalId":18845,"journal":{"name":"Nature Catalysis","volume":"7 9","pages":"977-986"},"PeriodicalIF":42.8000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.nature.com/articles/s41929-024-01198-1","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A bias-free photochemical diode, in which a p-type photocathode is connected to an n-type photoanode to harness light for driving photoelectrochemical reduction and oxidation pairs, serves as a platform for realizing light-driven fuel generation from CO2. However, the conventional design, in which cathodic CO2 reduction is coupled with the anodic oxygen evolution reaction (OER), requires substantial energy input. Here we present a photochemical diode device that harnesses red light (740 nm) to simultaneously drive biophotocathodic CO2-to-multicarbon conversion and photoanodic glycerol oxidation as an alternative to the OER to overcome the above thermodynamic limitation. The device consists of an efficient CO2-fixing microorganism, Sporomusa ovata, interfaced with a silicon nanowire photocathode and a Pt–Au-loaded silicon nanowire photoanode. This photochemical diode operates bias-free under low-intensity (20 mW cm−2) red light irradiation with ~80% Faradaic efficiency for both the cathodic and anodic products. This work provides an alternative photosynthetic route to mitigate excessive CO2 emissions and efficiently generate value-added chemicals from CO2 and glycerol. CO2 reduction to value-added products is an attractive strategy in sustainable chemistry. Now a photochemical diode simultaneously drives biophotocathodic CO2-to-multicarbon conversion and photoanodic glycerol oxidation under red light with a photocurrent density of ~1.2 mA cm−2 and a Faradaic efficiency of ~80%.

Abstract Image

Abstract Image

红光供电的硅纳米线生物光化学二极管,可同时实现二氧化碳还原和甘油增值
无偏压光化学二极管(p 型光电阴极与 n 型光电阳极相连,利用光驱动光电化学还原和氧化对)是实现光驱动二氧化碳燃料发电的平台。然而,阴极二氧化碳还原与阳极氧进化反应(OER)相结合的传统设计需要大量的能量输入。在这里,我们提出了一种光化学二极管装置,利用红光(740 纳米)同时驱动生物光阴极二氧化碳到多碳的转化和光阳极甘油氧化反应,以替代 OER,从而克服上述热力学限制。该装置由高效二氧化碳固定微生物 Sporomusa ovata 与硅纳米线光电阴极和铂-金负载硅纳米线光阳极连接组成。这种光化学二极管可在低强度(20 mW cm-2)红光照射下无偏压运行,阴极和阳极产物的法拉第效率约为 80%。这项工作提供了另一种光合作用途径,可减少过量的二氧化碳排放,并从二氧化碳和甘油中高效生成增值化学品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Nature Catalysis
Nature Catalysis Chemical Engineering-Bioengineering
CiteScore
52.10
自引率
1.10%
发文量
140
期刊介绍: Nature Catalysis serves as a platform for researchers across chemistry and related fields, focusing on homogeneous catalysis, heterogeneous catalysis, and biocatalysts, encompassing both fundamental and applied studies. With a particular emphasis on advancing sustainable industries and processes, the journal provides comprehensive coverage of catalysis research, appealing to scientists, engineers, and researchers in academia and industry. Maintaining the high standards of the Nature brand, Nature Catalysis boasts a dedicated team of professional editors, rigorous peer-review processes, and swift publication times, ensuring editorial independence and quality. The journal publishes work spanning heterogeneous catalysis, homogeneous catalysis, and biocatalysis, covering areas such as catalytic synthesis, mechanisms, characterization, computational studies, nanoparticle catalysis, electrocatalysis, photocatalysis, environmental catalysis, asymmetric catalysis, and various forms of organocatalysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信