{Reference Type}: Journal Article
{Title}: Pre-Coordination Induced Further Deamination to Create Inter-Chain Cross-Linking in Carbon Nitride for Enhanced Photocatalytic H2O2 Production.
{Author}: Zhang H;Wang Y;Gong J;Huang C;Guo Y;Sun J;Lei W;
{Journal}: Chemistry
{Volume}: 0
{Issue}: 0
{Year}: 2024 Jul 2
{Factor}: 5.02
{DOI}: 10.1002/chem.202401948
{Abstract}: Creating cross-linking to establish efficient inter-chain charge-transfer channels in carbon nitride represents a promising strategy for enhancing its photocatalytic capabilities. Molten salt-assisted calcining has emerged as a method for preparing cross-linked carbon nitrides. However, the precise influence of molten salts on the molecular structure of carbon nitride remains to be fully elucidated. Herein, we develop a KCl guided cross-linking reaction to preliminarily reveal the formation mechanism of cross-linking. The cross-linking reaction is initiated by the pre-coordination of amino groups with K+. Subsequent heating at high temperature converts the amino groups into chlorines. Then, dechlorination leads to the formation of cross-linking. Thus, this cross-linking reaction can be accurately described as a pre-coordination-induced, two-step deamination reaction. The pre-coordination step plays a pivotal role in the cross-linking process. Sufficient pre-coordination results in a relatively high cross-linking degree of the as-prepared CNK-2. Consequently, CNK-2 demonstrates a significantly enhanced photocatalytic H2O2 production, with a generation rate of 682 μmol·L-1·h-1, about 59 times that of traditional carbon nitride.