摘要：Optical manipulation of micro/nanoscale objects is of importance in life sciences,colloidal science,and *** tweezers exhibit superior manipulation capability at low optical ***,our implicit understanding of the working mechanism has limited the further applications and innovations of optothermal ***,we present an atomistic view of opto-thermo-electro-mechanic coupling in optothermal tweezers,which enables us to rationally design the tweezers for optimum performance in targeted ***,we have revealed that the non-uniform temperature distribution induces water polarization and charge separation,which creates the thermoelectric field dominating the optothermal *** further design experiments to systematically verify our atomistic *** by our new model,we develop new types of optothermal tweezers of high performance using low-concentrated ***,we demonstrate the use of new tweezers in opto-thermophoretic separation of colloidal particles of the same size based on the difference in their surface charge,which has been challenging for conventional optical *** the atomistic understanding that enables the performance optimization and function expansion,optothermal tweezers will further their impacts.

摘要：The advancement of photo-curing three-dimensional(3D)printing technology has significantly enhanced the capabilities of advanced manufacturing across various ***,the robust cross-linking network of photopolymers limits its application in information encryption and exacerbates environmental *** this study,a degradable thermosetting photopolymer platform for information encryption was proposed by incorporating sulfite bonds into the polymer *** to the autocatalytic behavior of sulfite bonds during hydrolysis under acidic conditions,the photopolymer can achieve complete degradation at 50℃ within 45 *** on the degradability of the developed photopolymers,a highly secure degradation-UV dual information encryption system has been established using photo-curing-based 3D printing ***,the degradation products of these photopolymers,generated during the information decryption process,can be utilized to prepare high-performance solar thermoelectric generators with a power density of 325.7µW cm^(−2)(under one sun)after a simple one-step *** work not only inspires the development of multiple information encryption methods based on 3D printing but also provides a practical solution to address environmental challenges associated with plastic pollution.

摘要：Noble metal-free electrocatalysts with high activity are highly desirable for the large-scale application of hydrogen evolution reaction(HER). Mo_(2) C-based nanomaterials have been proved as a promising alternative to noble metal-based electrocatalysts owing to the Pt-resembled d-band density and optimal intermediates-adsorption ***, the aggregation and excessive growth of crystals often occur during their high-temperature synthesis procedure, leading to low catalytic utilization. In this study, the ultrafine Mo_(2) C/Mo_(2) N heterostructure with large surface and interface confined in the N-doped carbon nanofibers(NCNFs) was obtained by a melamine-assisted method. The synergistic effect of Mo_(2) C/Mo_(2) N heterostructure and plenty active sites exposed on the surface of ultrafine nanocrystals improves the electrocatalytic activity. Meanwhile, the N-CNFs ensure fast charge transfer and high structural stability during reactions. Moreover, the in-situ synthesis method strengthens the interfacial coupling interactions between Mo_(2)C/Mo_(2) N heterostructure and N-CNFs, further enhancing the electronic conductivity and electrocatalytic activity. Owing to these advantages, Mo_(2)C/Mo_(2) N@N-CNFs exhibit excellent HER performance with a low overpotential of 75 mV at a current density of 10 mV cm^(-2) in alkaline solution, superior to the single-phased Mo_(2)C counterpart and recently reported Mo_(2)C/Mo_(2) N-based catalysts. This study highlights a new effective strategy to design efficient electrocatalysts via integrating heterostructure, nanostructure and carbon modification.