Graphene-based materials as electrocatalysts for the oxygen evolution reaction: a review
文献情報
Hwapyung Jung, Arindam Adhikari, Rajkumar Patel
The continuous depletion of fossil fuels makes it necessary to find out an appropriate alternative energy sources to fulfill the global energy requirement. During this search, it has been observed that ‘hydrogen’ with a specific energy density value of 142 kJ mol−1 can play an important role. Electrocatalytic water splitting is one of the ways to generate pure hydrogen by forming water molecules as an impurity. Electrocatalytic water splitting consists of two half-cell reactions, i.e., the oxygen evolution reaction (OER) at the anode and hydrogen evolution reaction (HER) at the cathode. Noble metal oxides (RuO2 and IrO2) and Pt metal are considered the state-of-art electrocatalysts for the OER and HER, respectively. However, the high cost and low abundance of these noble metal-based electrocatalysts have motivated the development of alternative electrocatalysts for the practical large-scale generation of hydrogen. Recently, various derivatives of transition metals have been considered as effective and low-cost alternatives to noble metal-based electrocatalysts. However, although various transition metal-based electrocatalysts have been reported thus far to exhibit excellent OER and HER activity, their low conductivity and marginal stability under static conditions require their modification to achieve better stability. Recently, the synthesis of graphene composites with transition metal-based electrocatalysts has gain an increased attention due to their excellent conductivity and stability with excellent hydrogen generation. Here, in this review, for the first time, we have discuss the recent development of various graphene-based composites of transition metals for the water splitting reaction. In addition, the current challenges and opportunities in this field will be discussed elaborately with an extensive future outlook.
関連文献
Evidence of carbon–carbon bond formation on GaAs(100) via Fischer–Tropsch methyleneinsertion reaction mechanism
Neil T. Kemp, Nagindar K. Singh
DOI: 10.1039/B506195D
Polydipyrrole- and polydicarbazole-nanorods as new nanosized supports for DNA hybridization
Jean-Paul Lellouche, Senthil Govindaraji, Augustine Joseph, Jyongsik Jang, Kyung Jin Lee
DOI: 10.1039/B502483H
Analysis of key steps in the catalytic cross-coupling of alkyl electrophiles under Negishi-like conditions
Gavin D. Jones, Chris McFarland, Thomas J. Anderson, David A. Vicic
DOI: 10.1039/B504996B
Polymer vesicles formed by amphiphilic diblock copolymers containing a thermotropic liquid crystalline polymer block
Jing Yang, Daniel Lévy, Wei Deng, Patrick Keller, Min-Hui Li
DOI: 10.1039/B508034G
Water-soluble organic dppz analogues—tuning DNA binding affinities, luminescence, and photo-redox properties
Tim Phillips, Chatna Rajput, Lance Twyman, Ihtshamul Haq, Jim A. Thomas
DOI: 10.1039/B506946G
Shape-dependent magnetic properties of low-dimensional nanoscale Prussian blue (PB) analogue SmFe(CN)6·4H2O
Hao-Ling Sun, Hongtao Shi, Fei Zhao, Limin Qi, Song Gao
DOI: 10.1039/B507240A
Dendritic supramolecular assemblies for drug delivery
Meredith T. Morgan, Michael A. Carnahan, Stella Finkelstein, Carla A. H. Prata, Lovorka Degoricija, Stephen J. Lee, Mark W. Grinstaff
DOI: 10.1039/B502411K
Electrochemical detection of Arachis hypogaea (peanut) agglutinin binding to monovalent and clustered lactosyl motifs immobilized on a polypyrrole film
Chantal Gondran, Olivier Renaudet, Pascal Dumy, Hugues Driguez, Sébastien Fort, Serge Cosnier
DOI: 10.1039/B506699A
Enantioselective organocatalytic Michael addition of malonate esters to nitroolefins using bifunctional cinchonine derivatives‡
Jinxing Ye, Darren J. Dixon, Peter S. Hynes
DOI: 10.1039/B508833J
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...














![2-Methylbenzo[h]quinoline structure 2-Methylbenzo[h]quinoline structure](https://static.chemtradehub.com/structs/605/605-88-9-ac43.webp)
