Microwave-assisted synthesis of ZIF-9@xGO composites as cooperative electrocatalysts for electro-oxidation of benzyl alcohols coupled with H2 production
文献情報
Sayantan Chongdar, Anirban Ghosh, Asim Bhaumik
Selective electrochemical oxidation of alcohols to their corresponding aldehydes or acids utilizing water as the oxygen source is not only considered a green and sustainable approach to synthesize value added chemicals but also economically demanding as the overall process is coupled with green H2 production. However, restricted production due to low current density and the use of expensive noble-metal-based electrocatalysts has limited its industrial viability. On the other hand microwave-assisted synthesis enables a rapid, economical and effective way to fabricate various advanced porous materials. In this regard, herein we report microwave assisted rapid synthesis of a metal–organic framework materials ZIF-9 nanocrystals and ZIF-9@xGO composites by varying the wt% of graphene oxide (GO). Remarkably, upon GO loading the current density increases significantly from 75 mA cm−2 to 204 mA cm−2 at 1.6 V vs. RHE in an alkaline solution with 0.1 M benzyl alcohol, thereby imparting direct impact towards benzoic acid yield (∼84%) and faradaic efficiency (∼88%) of the process. Moreover, the optimised electrocatalyst (i.e. ZIF-9@10GO) exhibits a H2 evolution rate of 273 mmol g−1 h−1 in the presence of benzyl alcohol. Our results indicate that in situ generated Co(OH)2/CoOOH hybrid species over the ZIF-9 surface plays an active role in this electrocatalysis. Additionally, this electrocatalytic system shows good functional group tolerance, exhibiting wide scope for different substrates with high faradaic efficiency.
おすすめジャーナル
関連文献
The synthesis of thermoresponsive POSS-based eight-arm star poly(N-isopropylacrylamide): A comparison between Z-RAFT and R-RAFT strategies
Bo Pang, Rui Liu, Guang Han, Wei Wang
DOI: 10.1039/D1PY00087J
Oxygen tolerant, photoinduced controlled radical polymerization approach for the synthesis of giant amphiphiles
Alexis Theodorou, Petros Mandriotis, Athina Anastasaki, Kelly Velonia
DOI: 10.1039/D0PY01608J
Structural design of pyrene-functionalized TEMPO-containing polymers for enhanced electrochemical storage performance
Hatice Mutlu, Hongjiao Li, Wolfgang Wenzel
DOI: 10.1039/D0PY01421D
Synthesis of fully degradable cationic polymers with various topological structures via postpolymerization modification by using thio-bromo “click” reaction
Yunkai Dai, Zhitao Hu, Xiaoying Wang, Xingliang Liu, Yuanchao Li, Yi Shi, Yongming Chen
DOI: 10.1039/D1PY00106J
Efficient synthesis of discrete oligo(fluorenediacetylene)s toward chain-length-dependent optical and structural properties
Xianheng Shi, Min Liu, Lishan Li, Jiandong Zhang, Haiyan Li, Zhihao Huang, Wei Zhang, Zhengbiao Zhang, Nianchen Zhou, Xiulin Zhu
DOI: 10.1039/D1PY00165E
Hollow microspherical carbazole-based conjugated polymers by photoinduced step-growth polymerization
Tugba Celiker, Ali Suerkan, Sinem Altinisik, Mert Akgun, Sermet Koyuncu
DOI: 10.1039/D1PY00822F
Nucleobase-monofunctionalized supramolecular poly(l-lactide): controlled synthesis, competitive crystallization, and structural organization
Xing Li, Lingling Ni, Chenxuan Sun, Wenqing Xu
DOI: 10.1039/D1PY00288K
こちらもおすすめ
噻奈普汀乙酯の物理化学的性質は何ですか?
CAS番号66981-77-9の噻奈普汀乙酯は、結晶性白色粉末であり、分子量は476.9 g/molです。この化合物は水に溶けにくく、一般的には有機溶媒で溶解し...
アミピシリン不純物Fとは何ですか?
アミピシリン不純物Fは、CAS番号124774-48-7の化合物です。これは、抗生物質アミピシリンの生産過程で生成される不純物の一つであり、(4S)-2-({[...
イリジウム(I)ヘキサフルオロフォスファートの代替品はありますか?
イリジウム(I)ヘキサフルオロフォスファートの代替品として、他の有機金属化合物や非有機金属化合物が使用されることがあります。具体的には、ダイゾニウム塩や他の金属...
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物はどのように処理すべきですか?
含有3-(苯氧基甲基)苯硼酸频那醇酯の廃棄物は、安全な方法で処理する必要があります。まず、廃棄物を適切な容器に収集し、避けて保管します。次に、専門の廃棄処理業者...
2-甲基辛-1-醇を取り扱う際の実験室安全事項は何ですか?
取り扱う際は、密閉のゴーグルと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用し、漏洩時には速やかに取り扱いを中止し、適切な排気設備を使用してください...
3α-アセトキノイドコレステロールエステルはどのように保存すればよいですか?
3α-アセトキノイドコレステロールエステルは、常温から低温(0-5℃)の暗所で保存し、密閉容器に入れることで安定性を保つことが推奨されます。また、湿気や酸素から...
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸の主な用途は何ですか?
2-ぶンジロキシ-4-(トリフルオロメチル)フェノルビノン酸は、化学合成の触媒としての使用や、医薬品の合成材料としての役割があります。また、特定の合成路線で使用...
(2S,3R)-2-氨基-3-甲基丁二酸はどのように合成されますか?
(2S,3R)-2-氨基-3-甲基丁二酸は、2-ヒドロキシ-3-メチル丁酸とアミノ化反応を行うことで合成されます。触媒としてジクロロメタンが使用され、選択性と収...
1-Benzyl-2-phenyl-1H-imidazoleはどのように保存すればよいですか?
この化合物は常温で避けてください。直射日光を避け、密閉容器で保存し、湿気を防水の容器に入れて保管してください。
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














![Methyl 8-azabicyclo[3.2.1]octane-3-carboxylate hydrochloride structure Methyl 8-azabicyclo[3.2.1]octane-3-carboxylate hydrochloride structure](https://static.chemtradehub.com/structs/179/179022-43-6-77f5.webp)