ReactorAFM/STM – dynamic reactions on surfaces at elevated temperature and atmospheric pressure

• Tycho Roorda,
• Hamed Achour,
• Matthijs A. van Spronsen,
• Marta E. Cañas-Ventura,
• Sander B. Roobol,
• Willem Onderwaater,
• Mirthe Bergman,
• Peter van der Tuijn,
• Gertjan van Baarle,
• Johan W. Bakker,
• Joost W. M. Frenken and
• Irene M. N. Groot

Beilstein J. Nanotechnol. 2025, 16, 397–406, doi:10.3762/bjnano.16.30

• water (m/z 18) indicating that the FTS reaction has started. After ≈1200 seconds, the water signal reaches a maximum. Hereafter, the temperature decreases, until reaching 490 K, where the reaction completely stops and the number of counts starts to significantly decrease. At 490 K, at which point the Co

• catalyst ceases its reactivity, the reaction stops. Furthermore, we observe maxima in masses of m/z 30, 44, and 86, representing ethane, propane, and hexane, respectively, in the same time frame as that for the observation of water formation. Conclusion The developments in the ReactorAFM/STM design prove

Emerging strategies in the sustainable removal of antibiotics using semiconductor-based photocatalysts

• Yunus Ahmed,
• Keya Rani Dutta,
• Parul Akhtar,
• Md. Arif Hossen,
• Md. Jahangir Alam,
• Obaid A. Alharbi,
• Hamad AlMohamadi and
• Abdul Wahab Mohammad

Beilstein J. Nanotechnol. 2025, 16, 264–285, doi:10.3762/bjnano.16.21

• ) that incorporate GO as a co-catalyst have been employed in the photocatalysis field to remove antibiotics. For instance, g-C3N4/Ag2CO3/GO [108], BiOBr/MoS2/GO [111], and g-C3N4/GO/CoFe2O4 [64]. rGO is also considered as a promising semiconductor material, but its characteristics can differ based on the

Influence of conductive carbon and MnCo₂O₄ on morphological and electrical properties of hydrogels for electrochemical energy conversion

• Sylwia Pawłowska,
• Karolina Cysewska,
• Yasamin Ziai,
• Jakub Karczewski,
• Piotr Jasiński and
• Sebastian Molin

Beilstein J. Nanotechnol. 2024, 15, 57–70, doi:10.3762/bjnano.15.6

• )porphyrin hydrogel) and PPy/FeTCPP/Co catalyst at 10 mA/cm2 current density, and in 0.1 M KOH, were 1.74 and 1.61 versus RHE, respectively (the catalyst loading equals to 0.3 mg/cm2) [55]. The analysis of , , and hydrogel catalysts in 1 M KOH for the OER process showed that the overpotential at a current

Bismuth-based nanostructured photocatalysts for the remediation of antibiotics and organic dyes

• Akeem Adeyemi Oladipo and
• Faisal Suleiman Mustafa

Beilstein J. Nanotechnol. 2023, 14, 291–321, doi:10.3762/bjnano.14.26

• charges and, hence, increase photocatalytic activity, metallic bismuth can function as a direct plasmonic photocatalyst (similar to Au and Ag) or a co-catalyst [77]. Also, the unique layered crystal structure of Aurivillius-type bismuth oxide-based semiconductors allows for the induction of an internal

Recent trends in Bi-based nanomaterials: challenges, fabrication, enhancement techniques, and environmental applications

• Vishal Dutta,
• Ankush Chauhan,
• Ritesh Verma,
• C. Gopalkrishnan and
• Van-Huy Nguyen

Beilstein J. Nanotechnol. 2022, 13, 1316–1336, doi:10.3762/bjnano.13.109

• potential role of Au nanoparticles in the S-scheme heterostructure is noteworthy. They serve as a co-catalyst for improving electron separation and transmission due to the photogenerated potential. By forming heterojunctions, the visible-light absorption as well as the carrier separation efficiency of Bi

Studies of probe tip materials by atomic force microscopy: a review

• Ke Xu and
• Yuzhe Liu

Beilstein J. Nanotechnol. 2022, 13, 1256–1267, doi:10.3762/bjnano.13.104

• prominent carbon nanotube tips. This type of process strategy is used to produce CNT tips in wafer-scale AFM. By identifying and manipulating the key growth conditions that control the density and length of carbon nanotube growth; i.e., the amount of Co catalyst and CNT growth time, it is possible to switch

Tin dioxide nanomaterial-based photocatalysts for nitrogen oxide oxidation: a review

• Viet Van Pham,
• Hong-Huy Tran,
• Thao Kim Truong and
• Thi Minh Cao

Beilstein J. Nanotechnol. 2022, 13, 96–113, doi:10.3762/bjnano.13.7

• , surface engineering, heterojunction construction, co-catalyst, which will be thoroughly outlined in this review. Structure and bandgap SnO2 has a crystal structure similar to that of rutile TiO2 [41][42]. The unit cell parameters of rutile SnO2 are a = b = 0.47374 nm and c = 0.31864 nm [43]. In one unit

Synthesis of novel C-doped g-C₃N₄ nanosheets coupled with CdIn₂S₄ for enhanced photocatalytic hydrogen evolution

• Jingshuai Chen,
• Chang-Jie Mao,
• Helin Niu and
• Ji-Ming Song

Beilstein J. Nanotechnol. 2019, 10, 912–921, doi:10.3762/bjnano.10.92

• transfer nanochannels [5]. The as-prepared g-C3N4 nanosheet@ZnIn2S4 nanoleaf structure displays an enhanced photocatalytic activity for H2 production without the addition of a Pt co-catalyst. As visible-light-active photocatalysts, ternary metal sulfide (e.g., ZnIn2S4 and CdIn2S4) have attracted great

• enhance photocatalytic activity. Accordingly, the two-step fabrication of CdIn2S4/CCN photocatalysts with different CdIn2S4 content is the target of this study. It is demonstrated that the CdIn2S4/CCN hybrid shows a superior H2 production activity without the addition of a Pt co-catalyst under visible

• use of the additive Pt co-catalyst. As shown in Figure 8, the pristine g-C3N4 presents a negligible H2 generation rate, but after introduction of the self-doped C by a simple supramolecular self-assembly method, the CCN nanosheets display a higher H2 generation rate due to the presence of the large

Cr(VI) remediation from aqueous environment through modified-TiO₂-mediated photocatalytic reduction

• Rashmi Acharya,
• Brundabana Naik and
• Kulamani Parida

Beilstein J. Nanotechnol. 2018, 9, 1448–1470, doi:10.3762/bjnano.9.137

Review on optofluidic microreactors for artificial photosynthesis

• Xiaowen Huang,
• Jianchun Wang,
• Tenghao Li,
• Jianmei Wang,
• Min Xu,
• Weixing Yu,
• Abdel El Abed and
• Xuming Zhang

Beilstein J. Nanotechnol. 2018, 9, 30–41, doi:10.3762/bjnano.9.5

• catalytic materials, modification of the existed catalytic materials (e.g., noble-gas doping, co-catalyst impregnation, noble-metal loading, plasmonic sensitization and Z-scheme systems), and optofluidics (or microfluidics) based APS. It should be noted that many efforts have been made to develop bio

One-step chemical vapor deposition synthesis and supercapacitor performance of nitrogen-doped porous carbon–carbon nanotube hybrids

• Egor V. Lobiak,
• Lyubov G. Bulusheva,
• Ekaterina O. Fedorovskaya,
• Yury V. Shubin,
• Pavel E. Plyusnin,
• Pierre Lonchambon,
• Boris V. Senkovskiy,
• Zinfer R. Ismagilov,
• Emmanuel Flahaut and
• Alexander V. Okotrub

Beilstein J. Nanotechnol. 2017, 8, 2669–2679, doi:10.3762/bjnano.8.267

• nickel hydroxide in hydrogen atmosphere [15]. The hybrid showed improved cycling stability in lithium–sulfur batteries as compared to the electrode made from porous carbon only. Cai et al. have synthesized N-doped hierarchical porous carbon–CNT hybrids using a melamine-formaldehyde resin, Fe/Co catalyst

High photocatalytic activity of Fe₂O₃/TiO₂ nanocomposites prepared by photodeposition for degradation of 2,4-dichlorophenoxyacetic acid

• Shu Chin Lee,
• Hendrik O. Lintang and
• Leny Yuliati

Beilstein J. Nanotechnol. 2017, 8, 915–926, doi:10.3762/bjnano.8.93

• of the best modifiers, the use of a co-catalyst has been recognized to improve the photocatalytic performance of semiconductor photocatalysts as it promotes charge separation and suppresses photocorrosion of the semiconductor photocatalyst [3][4]. One of the potential co-catalyst modifiers is iron

• /TiO2 heterojunction might promote better electron transfer which resulted in improved photocatalytic activity of the Fe2O3(0.5)/TiO2 (PD) material. Photoluminescence has been associated with electron–hole recombination of a photocatalyst [39]. In this study, the ability of an Fe2O3 co-catalyst to

• superoxide radical scavengers. The activity decreased 8.8 and 1.4 times, respectively, as compared to those on TiO2 (NT), i.e., 5.8 and 1.2 times, respectively. Such a result suggested the crucial role of Fe2O3 as a co-catalyst to improve the interfacial charge transfer and suppress electron–hole

Investigation of growth dynamics of carbon nanotubes

• Marianna V. Kharlamova

Beilstein J. Nanotechnol. 2017, 8, 826–856, doi:10.3762/bjnano.8.85

• recent works [113][119][120][123][124][125][126] succeeded in the selective growth of SWCNTs with chiralities that are different from (6,5). In [113][123], near-armchair SWCNTs with a chirality of (9,8) were selectively synthesized. The authors of [113] produced the SWCNT samples using Co catalyst on TUD

Enhanced photocatalytic hydrogen evolution by combining water soluble graphene with cobalt salts

• Jing Wang,
• Ke Feng,
• Hui-Hui Zhang,
• Bin Chen,
• Zhi-Jun Li,
• Qing-Yuan Meng,
• Li-Ping Zhang,
• Chen-Ho Tung and
• Li-Zhu Wu

Beilstein J. Nanotechnol. 2014, 5, 1167–1174, doi:10.3762/bjnano.5.128

• Photocatalytic hydrogen evolution from water-splitting is a long-standing goal for researchers since it can help to supply the growing worldwide energy demand not only environmentally friendly but also sustainably [1][2][3][4]. Platinum, the most efficient hydrogen evolution co-catalyst, is rare and expensive

• demonstrated that G-SO3 acts as an electron mediator of EY and platinum nanoparticles co-catalyst, we consider that in the current study the electron transfer process from the EY radical anion (EY•−) to G-SO3 or in situ formed-Co(TEOA)22+ would be facilitated. Similar to the storage phenomenon observed in

Enhancement of photocatalytic H₂ evolution of eosin Y-sensitized reduced graphene oxide through a simple photoreaction

• Weiying Zhang,
• Yuexiang Li,
• Shaoqin Peng and
• Xiang Cai

Beilstein J. Nanotechnol. 2014, 5, 801–811, doi:10.3762/bjnano.5.92

• investigated with eosin Y (EY) as a sensitizer of the RGO and Pt as a co-catalyst. When the irradiation time is increased from 0 to 24 h the activity rises, and then reaches a plateau. Under optimum conditions (pH 10.0, 5.0 × 10−4 mol L−1 EY, 10 μg mL−1 RGO), the maximal apparent quantum yield (AQY) of EY

• efficient electron relay between the photoexcited EY and the loaded Pt co-catalyst, which shows an AQY of 4.15% under visible light irradiation. In these works, RGO was obtained by a chemical reduction of GO with hydrazine or sodium borohydride as a reductant. Graphene, an atom-thick two-dimensional (2D

• controlling UV irradiation time. The RGO solution and its powder were denoted as RGOx and RGOx-p, respectively, where x (in hours) represents the particular UV irradiation time. The photocatalytic activity of EY-sensitized RGOx was investigated by using Pt as a co-catalyst and trimethylamine (TMA) as a

Nanostructure sensitization of transition metal oxides for visible-light photocatalysis

• Hongjun Chen and
• Lianzhou Wang

Beilstein J. Nanotechnol. 2014, 5, 696–710, doi:10.3762/bjnano.5.82

• role of a co-catalyst, which may act as electron sinks to draw them away from the holes and enhance their lifetimes [64]. Under visible light, the plasmonic nanostructures enhance the solar-light harvesting and increase the visible-light energy-conversion efficiency as photosensitizer. It is well-known

Preparation of NiS/ZnIn₂S₄ as a superior photocatalyst for hydrogen evolution under visible light irradiation

• Liang Wei,
• Yongjuan Chen,
• Jialin Zhao and
• Zhaohui Li

Beilstein J. Nanotechnol. 2013, 4, 949–955, doi:10.3762/bjnano.4.107

• for hydrogen evolution under visible light irradiation was also investigated. It was found that the photocatalytic hydrogen evolution activity over hexagonal ZnIn2S4 can be significantly increased by loading NiS as a co-catalyst. The formation of a good junction between ZnIn2S4 and NiS via the two

• loading amount of 0.5 wt %. This work demonstrates a high potential of the developing of environmental friendly, cheap noble-metal-free co-catalyst for semiconductor-based photocatalytic hydrogen evolution. Keywords: co-catalyst; hydrogen evolution; NiS; photocatalytic; photocatalysis; visible light

• ] or RGO [23] into ZnIn2S4 nanostructures, the photocatalytic performance for hydrogen evolution over ZnIn2S4 have been enhanced to a certain degree. Studies on semiconductor-based photocatalysts revealed that the deposition of a suitable co-catalyst on the semiconductor photocatalysts can play