@article{66419,
  abstract     = {{<jats:p>
                    C
                    <jats:sub>2</jats:sub>
                    N‐type carbon materials are typically obtained through high‐temperature treatment of nitrogen‐rich molecular precursors under inert atmosphere. Herein, we demonstrate mechanochemical approaches that enable the synthesis of C
                    <jats:sub>2</jats:sub>
                    N materials, namely by (i) the conversion of hexaazatriphenylenehexacarbonitrile (HAT‐CN) and by (ii) a one‐pot route starting from its molecular precursors, hexaketocyclohexane, and diaminomaleonitrile. Compared with conventional pyrolytic methods, mechanochemical approaches afford higher yields while significantly reducing energy input, thereby improving overall sustainability. The results highlight the decisive role of mechanical energy in directing carbon–nitrogen framework formation and demonstrate mechanochemistry as a versatile alternative to thermal routes for C
                    <jats:sub>2</jats:sub>
                    N synthesis.
                  </jats:p>}},
  author       = {{Dippner, Pascal and Grätz, Sven and Lins, Jonas and Gutmann, Torsten and Borchardt, Lars}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  number       = {{9}},
  publisher    = {{Wiley}},
  title        = {{{Mechanochemical Near‐Ambient Synthesis of C                    <sub>2</sub>                    N Materials From HAT‐CN and its Precursors}}},
  doi          = {{10.1002/cssc.70678}},
  volume       = {{19}},
  year         = {{2026}},
}

@article{62652,
  abstract     = {{<jats:p>Driven by the urgent need for a green, safe, and cost‐effective approach to producing H<jats:sub>2</jats:sub> and H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>—both highly valuable in green energy and environmental protection fields—piezocatalysis, which converts mechanical energy into valuable chemicals, has emerged as a promising solution. However, current catalyst systems face challenges due to the need for materials with both a strong piezoelectric effect and favorable catalytic activity. Herein, the construction of an oxidized carbon nitride (<jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub>) matrix anchored with TiO<jats:sub>2</jats:sub> nanoparticles via alkaline hydrothermal treatment is reported. Under ultrasonication, the <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub>/TiO<jats:sub>2</jats:sub> composite exhibits optimal performance under carefully controlled alkaline hydrothermal conditions. With a low concentration of Ba(OH)<jats:sub>2</jats:sub> during hydrothermal treatment, Ba(OH)<jats:sub>2</jats:sub> provides an alkaline medium, oxidizing the <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub> species and introducing structural defects into the <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub> framework. The disruption of the <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub> matrix, along with its interaction with TiO<jats:sub>2</jats:sub> nanoparticles, enhances the piezoelectric effect. Consequently, the oxidized <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub>/TiO<jats:sub>2</jats:sub> composite achieves a remarkable H<jats:sub>2</jats:sub> production rate of 4427.2 μmol g<jats:sup>−1</jats:sup> and an H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> production rate of 809.3 μmol g<jats:sup>−1</jats:sup> within 1 h without the addition of any sacrificial agents or cocatalysts. This work presents an effective strategy for the structural optimization of <jats:italic>g</jats:italic>‐C<jats:sub>3</jats:sub>N<jats:sub>4</jats:sub>‐based materials and may inspire new approaches for designing advanced piezocatalysts.</jats:p>}},
  author       = {{Pan, Ying and Liao, Luocheng and Zhang, Xinwen and Liu, Yunya and Su, Ran and Lopez Salas, Nieves}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  number       = {{19}},
  publisher    = {{Wiley}},
  title        = {{{Oxidation‐Enhanced Piezocatalytic Activity in Carbon Nitride‐Based Catalysts for Hydrogen and Hydrogen Peroxide Production}}},
  doi          = {{10.1002/cssc.202500980}},
  volume       = {{18}},
  year         = {{2025}},
}

@article{64045,
  abstract     = {{Abstract In this work, we report on an improved cell assembly of cylindrical electrochemical cells for 23Na in-situ solid-state NMR (ssNMR) investigations. The cell set-up is suitable for using powder electrode materials. Reproducibility of our cell assembly is analyzed by preparing two cells containing hard carbon (HC) powder as working electrode and sodium metal as reference electrode. Electrochemical storage properties of HC powder electrode derived from carbonization of sustainable cellulose are studied by ssNMR. 23Na in-situ ssNMR monitors the sodiation/desodiation of a Na{\textbar}NaPF6{\textbar}HC cell (cell 1) over a period of 22?days, showing high cell stability. After the galvanostatic process, the HC powder material is investigated by high resolution 23Na ex-situ MAS NMR. The formation of ionic sodium species in different chemical environments is obtained. Subsequently, a second Na{\textbar}NaPF6{\textbar}HC cell (cell 2) is sodiated for 11?days achieving a capacity of 220?mAh/g. 23Na ex-situ MAS NMR measurements of the HC powder material extracted from this cell clearly indicate the presence of quasi-metallic sodium species next to ionic sodium species. This observation of quasi-metallic sodium species is discussed in terms of the achieved capacity of the cell as well as of side reactions of sodium in this electrode material.}},
  author       = {{Šić, Edina and Schutjajew, Konstantin and Haagen, Ulrich and Breitzke, Hergen and Oschatz, Martin and Buntkowsky, Gerd and Gutmann, Torsten}},
  issn         = {{1864-5631}},
  journal      = {{Chemsuschem}},
  keywords     = {{solid-state nmr, hard carbon, electrochemical cells, in-situ characterization, sodium}},
  pages        = {{e202301300}},
  publisher    = {{John Wiley & Sons, Ltd}},
  title        = {{{Electrochemical Sodium Storage in Hard Carbon Powder Electrodes Implemented in an Improved Cell Assembly: Insights from In-Situ and Ex-Situ Solid-State NMR}}},
  doi          = {{10.1002/cssc.202301300}},
  volume       = {{17}},
  year         = {{2023}},
}

@article{64044,
  abstract     = {{Abstract Polymer-derived silicon oxycarbide ceramics (SiCO) have been considered as potential anode materials for lithium- and sodium-ion batteries. To understand their electrochemical storage behavior, detailed insights into structural sites present in SiCO are required. In this work, the study of local structures in SiCO ceramics containing different amounts of carbon is presented. 13C and 29Si solid-state MAS?NMR spectroscopy combined with DFT calculations, atomistic modeling, and EPR investigations, suggest significant changes in the local structures of SiCO ceramics even by small changes in the material composition. The provided findings on SiCO structures will contribute to the research field of polymer-derived ceramics, especially to understand electrochemical storage processes of alkali metal/ions such as Na/Na+ inside such networks in the future.}},
  author       = {{Šić, Edina and Rohrer, Jochen and Ricohermoso, Emmanuel and Albe, Karsten and Ionescu, Emmanuel and Riedel, Ralf and Breitzke, Hergen and Gutmann, Torsten and Buntkowsky, Gerd}},
  issn         = {{1864-5631}},
  journal      = {{Chemsuschem}},
  keywords     = {{NMR spectroscopy, Ceramics, defects, density functional calculations, EPR spectroscopy}},
  pages        = {{e202202241}},
  publisher    = {{John Wiley & Sons, Ltd}},
  title        = {{{SiCO Ceramics as Storage Materials for Alkali Metals/Ions: Insights on Structure Moieties from Solid-State NMR and DFT Calculations}}},
  doi          = {{10.1002/cssc.202202241}},
  volume       = {{16}},
  year         = {{2023}},
}

@article{62810,
  abstract     = {{Cobalt iron containing layered double hydroxides (LDHs) and spinels are promising catalysts for the electrochemical oxygen evolution reaction (OER). Towards development of better performing catalysts, the precise tuning of mesostructural features such as pore size is desirable, but often hard to achieve. Herein, a computer‐controlled microemulsion‐assisted co‐precipitation (MACP) method at constant pH is established and compared to conventional co‐precipitation. With MACP, the particle growth is limited and through variation of the constant pH during synthesis the pore size of the as‐prepared catalysts is controlled, generating materials for the systematic investigation of confinement effects during OER. At a threshold pore size, overpotential increased significantly. Electrochemical impedance spectroscopy (EIS) indicated a change in OER mechanism, involving the oxygen release step. It is assumed that in smaller pores the critical radius for gas bubble formation is not met and therefore a smaller charge‐transfer resistance is observed for medium frequencies.}},
  author       = {{Rabe, Anna and Jaugstetter, Maximilian and Hiege, Felix and Cosanne, Nicolas and Ortega, Klaus Friedel and Linnemann, Julia and Tschulik, Kristina and Behrens, Malte}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{electrocatalysis, oxygen evolution reaction, cobalt spinel, cobalt hydroxide, LDH}},
  number       = {{10}},
  publisher    = {{Wiley}},
  title        = {{{Tailoring Pore Size and Catalytic Activity in Cobalt Iron Layered Double Hydroxides and Spinels by Microemulsion‐Assisted pH‐Controlled Co‐Precipitation}}},
  doi          = {{10.1002/cssc.202202015}},
  volume       = {{16}},
  year         = {{2023}},
}

@article{37950,
  author       = {{Hu, Yuya and Wei, Zhihong and Frey, Anna and Kubis, Christoph and Ren, Chang‐Yue and Spannenberg, Anke and Jiao, Haijun and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1}},
  number       = {{1}},
  pages        = {{363--372}},
  publisher    = {{Wiley}},
  title        = {{{Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO<sub>2</sub> with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts}}},
  doi          = {{10.1002/cssc.202002267}},
  volume       = {{14}},
  year         = {{2021}},
}

@article{40576,
  author       = {{Kossmann, Janina and Heil, Tobias and Antonietti, Markus and Lopez Salas, Nieves}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry}},
  number       = {{24}},
  pages        = {{6643--6650}},
  publisher    = {{Wiley}},
  title        = {{{Guanine‐Derived Porous Carbonaceous Materials: Towards C            <sub>1</sub>            N            <sub>1</sub>}}},
  doi          = {{10.1002/cssc.202002274}},
  volume       = {{13}},
  year         = {{2020}},
}

@article{37953,
  author       = {{Hu, Yuya and Peglow, Sandra and Longwitz, Lars and Frank, Marcus and Epping, Jan Dirk and Brüser, Volker and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T2, T1, CSSD}},
  number       = {{7}},
  pages        = {{1825--1833}},
  publisher    = {{Wiley}},
  title        = {{{Plasma‐Assisted Immobilization of a Phosphonium Salt and Its Use as a Catalyst in the Valorization of CO            <sub>2</sub>}}},
  doi          = {{10.1002/cssc.201903384}},
  volume       = {{13}},
  year         = {{2020}},
}

@article{41032,
  author       = {{Gregori, Bernhard J. and Schwarzhuber, Felix and Pöllath, Simon and Zweck, Josef and Fritsch, Lorena and Schoch, Roland and Bauer, Matthias and Jacobi von Wangelin, Axel}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry}},
  number       = {{16}},
  pages        = {{3864--3870}},
  publisher    = {{Wiley}},
  title        = {{{Stereoselective Alkyne Hydrogenation by using a Simple Iron Catalyst}}},
  doi          = {{10.1002/cssc.201900926}},
  volume       = {{12}},
  year         = {{2019}},
}

@article{37963,
  author       = {{Büttner, Hendrik and Kohrt, Christina and Wulf, Christoph and Schäffner, Benjamin and Groenke, Karsten and Hu, Yuya and Kruse, Daniela and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T4, CSSD}},
  number       = {{12}},
  pages        = {{2701--2707}},
  publisher    = {{Wiley}},
  title        = {{{Life Cycle Assessment for the Organocatalytic Synthesis of Glycerol Carbonate Methacrylate}}},
  doi          = {{10.1002/cssc.201900678}},
  volume       = {{12}},
  year         = {{2019}},
}

@article{37978,
  author       = {{Büttner, Hendrik and Steinbauer, Johannes and Wulf, Christoph and Dindaroglu, Mehmet and Schmalz, Hans-Günther and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{6}},
  pages        = {{1076--1079}},
  publisher    = {{Wiley}},
  title        = {{{Organocatalyzed Synthesis of Oleochemical Carbonates from CO<sub>2</sub>and Renewables}}},
  doi          = {{10.1002/cssc.201601163}},
  volume       = {{10}},
  year         = {{2017}},
}

@article{37974,
  author       = {{Steinbauer, Johannes and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T3, CSSD}},
  number       = {{15}},
  pages        = {{3025--3029}},
  publisher    = {{Wiley}},
  title        = {{{Poly(ethylene glycol)s as Ligands in Calcium-Catalyzed Cyclic Carbonate Synthesis}}},
  doi          = {{10.1002/cssc.201700788}},
  volume       = {{10}},
  year         = {{2017}},
}

@article{41048,
  author       = {{Schoch, Roland and Bauer, Matthias}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry}},
  number       = {{15}},
  pages        = {{1996--2004}},
  publisher    = {{Wiley}},
  title        = {{{Pollution Control Meets Sustainability: Structure-Activity Studies on New Iron Oxide-Based CO Oxidation Catalysts}}},
  doi          = {{10.1002/cssc.201600508}},
  volume       = {{9}},
  year         = {{2016}},
}

@article{37993,
  author       = {{Büttner, Hendrik and Steinbauer, Johannes and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{16}},
  pages        = {{2655--2669}},
  publisher    = {{Wiley}},
  title        = {{{Synthesis of Cyclic Carbonates from Epoxides and Carbon Dioxide by Using Bifunctional One-Component Phosphorus-Based Organocatalysts}}},
  doi          = {{10.1002/cssc.201500612}},
  volume       = {{8}},
  year         = {{2015}},
}

@article{37997,
  author       = {{Kohrt, Christina and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{12}},
  pages        = {{2031--2034}},
  publisher    = {{Wiley}},
  title        = {{{Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO<sub>2</sub>with Epoxides}}},
  doi          = {{10.1002/cssc.201500128}},
  volume       = {{8}},
  year         = {{2015}},
}

@article{37990,
  author       = {{Desens, Willi and Kohrt, Christina and Frank, Marcus and Werner, Thomas}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{22}},
  pages        = {{3815--3822}},
  publisher    = {{Wiley}},
  title        = {{{Highly Efficient Polymer-Supported Catalytic System for the Valorization of Carbon Dioxide}}},
  doi          = {{10.1002/cssc.201501119}},
  volume       = {{8}},
  year         = {{2015}},
}

@article{40593,
  author       = {{Lopez Salas, Nieves and del Monte, Francisco and Tamayo, Aitana and Fierro, José Luís G. and De Lacey, Antonio L. and Ferrer, M. Luisa and Gutiérrez, María C.}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry}},
  number       = {{12}},
  pages        = {{3347--3355}},
  publisher    = {{Wiley}},
  title        = {{{Sulfur-Doped Carbons Prepared from Eutectic Mixtures Containing Hydroxymethylthiophene as Metal-Free Oxygen Reduction Catalysts}}},
  doi          = {{10.1002/cssc.201402753}},
  volume       = {{7}},
  year         = {{2014}},
}

@article{38000,
  author       = {{Werner, Thomas and Büttner, Hendrik}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{T1, T2, CSSD}},
  number       = {{12}},
  pages        = {{3268--3271}},
  publisher    = {{Wiley}},
  title        = {{{Phosphorus-based Bifunctional Organocatalysts for the Addition of Carbon Dioxide and Epoxides}}},
  doi          = {{10.1002/cssc.201402477}},
  volume       = {{7}},
  year         = {{2014}},
}

@article{41255,
  author       = {{Jennerjahn, Reiko and Jackstell, Ralf and Piras, Irene and Franke, Robert and Jiao, Haijun and Bauer, Matthias and Beller, Matthias}},
  issn         = {{1864-5631}},
  journal      = {{ChemSusChem}},
  keywords     = {{General Energy, General Materials Science, General Chemical Engineering, Environmental Chemistry}},
  number       = {{4}},
  pages        = {{734--739}},
  publisher    = {{Wiley}},
  title        = {{{Benign Catalysis with Iron: Unique Selectivity in Catalytic Isomerization Reactions of Olefins}}},
  doi          = {{10.1002/cssc.201100404}},
  volume       = {{5}},
  year         = {{2012}},
}

