Enhancing photocatalytic CO2 reduction to formate through one-pot self-assembly of a semiartificial cell
文献情報
Yixin Hong, Jianyu Han, Zhi Wang, Xiaofei Gu, Tianyi Huang, Yafeng Wu, Songqin Liu
Enzymatic CO2 conversion by photocatalysis that mimics natural photosystems offers an eco-friendly method for transforming CO2 into valuable chemicals or fuels at a low cost. However, the primary challenge in artificial enzymatic conversion arises from the high energy loss caused by low electron transfer efficiency and the instability of enzymes due to the incompatibility between enzyme catalysts and photocatalysts. Integrating natural enzymes, photoharvesting component and electron mediators to build a semiartificial photosynthetic cell surpasses the natural photosynthetic system in terms of simplicity, directed charge transfer, altered enzyme conformation and light utilization efficiency. Herein, a semiartificial cell is constructed by co-assembly of photoantennas and enzymes on stacked nanorods within microspheres. The microspheres, formed through L-cystine self-assembly with excellent biocompatibility, facilitates the alteration of FDH to a conformation with an open active site cleft, exposing more active sites. The electron mediator (1-ethylamino-4,4′-bipyridine) is connected to meso-tetra(4-carboxyphenyl) porphyrin via an amide bond to enhance electron transport efficiency. By leveraging these attributes, formate production reaches 1.24 mmol gcat−1, and the semiartificial cell exhibits long-term durability.
関連文献
Non-equilibrium magnetic properties of a mixed spin (1/2, 1) Ising graphene nanoisland
Bayram Deviren, Seyma Akkaya Deviren, Tevfik Fikret Yagmuroglu
DOI: 10.1039/D3CP04785G
Janus layers and electronic structure of 1T-(TiSeS)2
Yue Lou
DOI: 10.1039/D3CP04958B
Giant exchange bias field above room temperature in perovskite YbCr1−xFexO3 (x = 0.6–0.9)
Kang Zhao, Dao Wang, Sajjad Ur Rehman
DOI: 10.1039/D3CP04883G
Growth mechanism prediction for nanoparticles via structure matching polymerization
Yi-Rong Liu, Yan Jiang
DOI: 10.1039/D3CP04702D
Composition dependence of X-ray stability and degradation mechanisms at lead halide perovskite single crystal surfaces
Alberto García-Fernández, Stefania Riva, Håkan Rensmo
DOI: 10.1039/D3CP05061K
Predicting the pair correlation functions of silicate and borosilicate glasses using machine learning
Kumar Ayush, Pooja Sahu, Sk. Musharaf Ali, Tarak K. Patra
DOI: 10.1039/D3CP05136F
Analysing the stability of He-filled hydrates: how many He atoms fit in the sII crystal?
Raquel Yanes-Rodríguez, Rita Prosmiti
DOI: 10.1039/D3CP05410A
The effect of weak π–π interactions on single-molecule electron transport properties of the tetraphenylethene molecule and its derivatives: a first-principles study
Zhiye Wang, Yunchuan Li, Mingjun Sun
DOI: 10.1039/D3CP04593E
Solar-driven electrochemical NH3 splitting into H2 and N2 on BiVO4-based photoanodes
Miwako Teranishi, Shin-ichi Naya, Hiroaki Tada
DOI: 10.1039/D3SE01513K
こちらもおすすめ
2-メトキシ-4-(メチルスルフィニル)アミンの主な用途は何ですか?
2-メトキシ-4-(メチルスルフィニル)アミンは、主に医薬品および農薬の製造に使用されます。また、合成化学の一部として研究用材料としても利用されます。
4,6-二氯-N-甲基ピラミジンアミンの代替品はありますか?
代替品としては、4,6-二クロロピラミジンアミンや他のピラミジン系化合物が考えられます。ただし、目的と用途によって最適な代替品は異なります。
6-氯-4-甲基-1H-吲哚を含む廃棄物はどのように処理すべきですか?
6-氯-4-甲基-1H-吲哚の廃棄物は、適切な容器に収集し、密閉して保管します。温度は常温、湿度は低く、直射日光を避けて保管することを推奨します。廃棄処理は専門...
2-フローユロ-4-(トリフルオロメチル)ベンゾイドについて「に適用される法規ガイドラインは何ですか」
2-フローユロ-4-(トリフルオロメチル)ベンゾイドのCAS番号は207974-08-1です。この化合物はGHS分類で毒性物質と有害な反応物質として分類されます...
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸はどのように保存すればよいですか?
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸は、室温で暗所に保管し、乾燥した環境で保存することを推奨します。容器は密閉性の...
イソデスロラタドリンの代替品はありますか?
イソデスロラタドリンの代替品としては、デスロラタドリンや他の抗ヒスタミン薬が挙げられます。具体的には、デスロラタドリン、ラセカミド、フェルタドリンなどが、症状や...
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐はどのように合成されますか?
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐の一般的な合成方法は、メタノール中で5-メトキシ-1,2,3,4-四ヒュドロイソキシンを塩酸で塩化します。この反応で...
4-アミノ-5-メトキシ-2-トルエンサルホニック酸についての法規ガイドラインは何ですか?
CAS番号6471-78-9の4-アミノ-5-メトキシ-2-トルエンサルホニック酸は、GHS分類では corrosive(腐食性)と識別されます。EUのREAC...
甲基孕酮を取り扱う際の実験室安全事項は何ですか?
甲基孕酮の取り扱いは、PPE(個人保護具)の使用が必要な重要な安全事項を伴います。防塵マスク、ゴーグル、手袋を着用することが推奨されます。ドラフトチャンバーを使...
掲載誌
Journal of Materials Chemistry A

Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. The journals have a strong history of publishing quality reports of interest to interdisciplinary communities and providing an efficient and rigorous service through peer review and publication. The journals are led by an international team of Editors-in-Chief and Associate Editors who are all active researchers in their fields. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C. More than one Journal of Materials Chemistry journal may be suitable for certain fields and researchers are encouraged to submit their paper to the journal that they feel best fits for their particular article. Example topic areas within the scope of Journal of Materials Chemistry A are listed below. This list is neither exhaustive nor exclusive. Artificial photosynthesis Batteries Carbon dioxide conversion Catalysis Fuel cells Gas capture/separation/storage Green/sustainable materials Hydrogen generation Hydrogen storage Photocatalysis Photovoltaics Self-cleaning materials Self-healing materials Sensors Supercapacitors Thermoelectrics Water splitting Water treatment










![4-[(2-{2-[2-(2-Aminoethoxy)ethoxy]ethoxy}ethyl)amino]-2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione structure 4-[(2-{2-[2-(2-Aminoethoxy)ethoxy]ethoxy}ethyl)amino]-2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione structure](https://static.chemtradehub.com/structs/209/2093416-31-8-3162.webp)
![2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure 2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure](https://static.chemtradehub.com/structs/127/1279090-25-3-1b84.webp)


![2-(7,7-Difluorobicyclo[4.1.0]hept-1-yl)ethanamine structure 2-(7,7-Difluorobicyclo[4.1.0]hept-1-yl)ethanamine structure](https://static.chemtradehub.com/structs/209/2098065-08-6-ff24.webp)