Gao Qing (Max) Lu

The electrochemical co-reduction of CO₂ and nitrate provides a sustainable route for urea synthesis via C–N coupling, yet kinetic limitations and poor intermediate interactions hinder urea yields. Here, we engineer a nano-confined CuRu bimetallic catalyst within mesoporous carbon hollow spheres (MCHS) to overcome these barriers. By spatially confining reactants and intermediates, the catalyst achieves a urea yield of 12.51 g h^–1 g_cat^–1 at 250 mA cm^–2, with 125-hour stability. In situ spectroscopy and computational analyses reveal that nano-confinement switches the C–N coupling pathway from the thermodynamically favored *COOH–*NH₂ to kinetically driven *OCO–*NO intermediates, bypassing energy barriers. Precise pore-size engineering (4–11 nm) demonstrates that optimal confinement simultaneously enhances reactant transport and intermediate retention, boosting selectivity. This work establishes nano-confinement as a versatile approach for controlling multi-step electrocatalytic processes, enabling sustainable chemical synthesis.

There is a strong desire to design and synthesize catalysts that assemble at the oil–water interface to improve the efficiency of biphasic reactions. Anisotropic dumbbell‐shaped bi‐component mesoporous carbon–organosilica Janus particles with asymmetric wettability are synthesized through a one‐step compartmentalized growth of a mesoporous organosilica sphere attached to a mesoporous resorcinol–formaldehyde (RF) sphere. A library was prepared of tunable Janus particles possessing diverse hollow structures with various functionalities. As a proof of concept, the Janus particle‐derived catalyst can assemble at the oil–water interface to stabilize Pickering emulsions. Owing to the increased reaction interface area, the Janus catalyst exhibits a more than three‐fold increase in catalytic efficiency compared to the Pt loaded carbon sphere catalyst in aqueous hydrogenation reactions.

There is a strong desire to design and synthesize catalysts that assemble at the oil–water interface to improve the efficiency of biphasic reactions. Anisotropic dumbbell‐shaped bi‐component mesoporous carbon–organosilica Janus particles with asymmetric wettability are synthesized through a one‐step compartmentalized growth of a mesoporous organosilica sphere attached to a mesoporous resorcinol–formaldehyde (RF) sphere. A library was prepared of tunable Janus particles possessing diverse hollow structures with various functionalities. As a proof of concept, the Janus particle‐derived catalyst can assemble at the oil–water interface to stabilize Pickering emulsions. Owing to the increased reaction interface area, the Janus catalyst exhibits a more than three‐fold increase in catalytic efficiency compared to the Pt loaded carbon sphere catalyst in aqueous hydrogenation reactions.

Surfactant-free CuAgSe nanoparticles were successfully synthesized on a large scale within a short reaction time via a simple environmentally friendly aqueous approach under room temperature. The nanopowders obtained were consolidated into pellets for investigation of their thermoelectric properties between 3 and 623 K. The pellets show strong metallic characteristics below 60 K and turn into an n-type semiconductor with increasing temperature, accompanied by changes in the crystal structure (i.e., from the pure tetragonal phase into a mixture of tetragonal and orthorhombic phases), the electrical conductivity, the Seebeck coefficient, and the thermal conductivity, which leads to a figure of merit (ZT) of 0.42 at 323 K. The pellets show further interesting temperature-dependent transition from n-type into p-type in electrical conductivity arising from phase transition (i.e., from the mixture phases into cubic phase), evidenced by the change of the Seebeck coefficient from −28 μV/K into 226 μV/K at 467 K. The ZT value increased with increasing temperature after the phase transition and reached 0.9 at 623 K. The sintered CuAgSe pellets also display excellent stability, and there is no obvious change observed after 5 cycles of consecutive measurements. Our results demonstrate the potential of CuAgSe to simultaneously serve (at different temperatures) as both an n-type and a p-type thermoelectric material.

The year 2014 may prove to be a major turning point in China's development of world-class science and innovation system. At the mid-term juncture of China's Medium- and Long-Term Program (MLP) for Science and Technology (S&T) development, the Ministry of Science and Technology conducted a comprehensive review and assessment of the program, accompanied by a two-day workshop and assessment meeting by a 12-member international evaluation team during 17–19 January. My observations as a panel member are as follows.