Complete metal‐free P‐functionalized carbon nanomaterials are synthesized from a single molecular precursor, phytic acid, for photocatalytic solar H2 production and simultaneous organic transformation of 4‐methyl benzyl alcohol to 4‐methyl benzaldehyde by managing the complete redox cycle. It is observed that by increasing the carbonization time, P‐functionalized amorphous carbon dots convert to the highly defined 2D sheet‐like nanostructure with optimum P‐functionality, resulting in efficient light absorption, charge separation, and improved active sites for photocatalysis. Finally, the highly defined sheet‐like structure converts to a more defected aggregated form, resulting in the depletion of photocatalytic efficiency. The structural and elemental features are further correlated with the ongoing photophysics by means of steady‐state and time‐resolved fluorescence spectroscopy. Transient photocurrent responses and Mott‐Schottky plots directly support the optimization of P‐functionalized carbon nanostructure for efficient photocatalysis. Finally, the detailed computational studies are carried out to unveil the charge separation mechanism and the crucial role of P‐functionalities as active sites for better charge accumulation as well as H2O adsorption on the surface. Overall, the in‐depth structure–property correlation and critical optimization of the heteroatom functionalized carbon nanomaterials will open up new possibilities for further development of metal‐free photocatalysts for solar‐energy conversion devices.

It is highly desirable to design cost-efficient and eco-friendly fluorometric sensors that can efficiently detect water contamination in D2O and other expensive organic solvents. Herein, we have synthesized N,P-codoped carbon dots (N,P-CDs) from o-phenylene diamine (o-PDA) and H3PO4 through the bottom-up carbonization method. Heteroatom co-doping increases the absorption cross section in the visible-NIR range, followed by the formation of stable emissive states in longer-wavelength regions. We have critically investigated the noncovalent interactions (especially H-bonding interactions) of various surface functional groups with surrounding solvent media through a detailed structure-property correlation. Based on the sensitivity of noncovalent H-bonding interactions to the stability of longer-wavelength emissive domains, we have utilized these N,P-CDs as cost-effective fluorometric sensors of water/moisture contamination in D2O especially under visible-NIR light; the optical sensitivity reaches up to 0.1 volume (%) level. The detailed sensing mechanism has been further supported by a computational study through a simple visualization approach by mapping and analyzing all possible noncovalent interactions between the CDs and the solvent medium.

Unlike the traditional fluorescent material, carbon dots (CDs) have unique photoluminescent properties, which directly depend on several synthesis parameters during the bottom-up carbonization process. Overall photoluminescence properties of CDs are mainly regulated by the three major emissive domains of CDs, that is, (a) small molecular fluorophores, (b) graphitic aromatic domains, and (c) amorphous domains and/or surface states. However, the extent of carbonization is extremely crucial as it directs the relative populations of the three emissive domains and their interplay, which eventually regulates the overall photo-physics of carbon-based nanomaterials. Therefore, it is highly desirable to explore the molecular-level stepwise transformations of small precursor molecules to zero-dimensional CDs and eventually their critical optimization in emitting, catalytic, and optoelectronic devices. Herein, we have investigated the stepwise growth process of zero-dimensional N-functionalized CDs from small molecular precursors–citric acid and ammonia. In-depth molecular insight into the evolution of chromophore centers has been gained through detailed structure–property correlation. Structural and elemental features have been illustrated by employing proton nuclear magnetic resonance, Fourier-transform infrared, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy. Furthermore, the intrinsic molecular-level transformation of CDs is nicely correlated with the evolution of the intriguing photophysical properties by detailed steady-state and time-resolved spectroscopy. In addition, the extent of aromaticity and the internal rigidity during the growth process have also been illustrated by temperature-dependent fluorescence spectroscopy. Overall, the current fundamental study will be extremely crucial for the development of CDs and their molecular-level optimization for on-demand applications.