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Emulsifiers derived from renewable resources such as sucrose and fatty acids are high volume commodity chemicals and currently produced by traditional chemical synthesis techniques that lack the capacity to form the most desirable monoesters (of sucrose) in a selective and efficient fashion. The development of new emulsifiers (surfactants) from alternate, structurally simpler but nevertheless abundant disaccharides such as maltose represents a possible solution to this problem. Herein, we report the facile enzymatic preparation of a homologous series of 6'- O-acylmaltose esters and an in-depth evaluation of them revealing that their surfactant properties and thermal stabilities are largely determined by the length of the fatty acid chain. In the first such comparison, we show that the foaming and emulsifying effects of certain of these maltose monoesters are superior to those of their sucrose-derived and commercially exploited counterparts. As such, maltose esters have considerable potential as emulsifiers for use in, for example, the food industry.

We present a topological conversion method to prepare O-incorporated CoP (O-CoP) nanorods. Due to the 1D structure and incorporated O atoms, the O-CoP-3 nanorods exhibit superior electrocatalytic performance towards the HER.

The exploration of high-efficiency, cost-effective and earth-abundant non-noble metal electrocatalysts toward oxygen evolution reaction (OER) is of vital importance for the advancement of renewable energy conversion technologies. Herein, we report...