Optical tweezers (OTs) and optical spanners (OSs) are powerful tools of optical manipulation, which are responsible for particle trapping and rotation, respectively. Conventionally, the OT and OS are built using bulky three-dimensional devices, such as microscope objectives and spatial light modulators. Recently, metasurfaces are proposed for setting up them on a microscale platform, which greatly miniaturizes the systems. However, the realization of both OT and OS with one identical metasurface is posing a challenge. Here, we offer a metasurface-based solution to integrate the OT and OS. Using the prevailing approach based on geometric and dynamic phases, we show that it is possible to construct an output field, which promises a high-numerical-aperture focal spot, accompanied with a coaxial vortex. Optical trapping and rotation are numerically demonstrated by estimating the mechanical effects on a particle probe. Moreover, we demonstrate an on-demand control of the OT-to-OS distance and the topological charge possessed by the OS. By revealing the OT–OS metasurfaces, our results may empower advanced applications in on-chip particle manipulation.

We developed adjustable and movable droplet microlenses consisting of a liquid with a high refractive index. The microlenses were prepared via ultrasonic shaking in deionized water, and the diameter of the microlenses ranged from 1 to 50 μm. By stretching the microlenses, the focal length can be adjusted from 13 to 25 μm. With the assistance of an optical tweezer, controllable assembly and movement of microlens arrays were also realized. The results showed that an imaging system combined with droplet microlenses could image 80 nm beads under white light illumination. Using the droplet microlenses, fluorescence emission at 550 nm from CdSe@ZnS quantum dots was efficiently excited and collected. Moreover, Raman scattering signals from a silicon wafer were enhanced by ～19 times. The presented droplet microlenses may offer new opportunities for flexible liquid devices in subwavelength imaging and detection.

We report on the optical trapping and orientation of Escherichia coli (E. coli) cells using two tapered fiber probes. With a laser beam at 980 nm wavelength launched into probe I, an E. coli chain consisting of three cells was formed at the tip of probe I. After launching a beam at 980 nm into probe II, the E. coli at the end of the chain was trapped and oriented via the optical torques yielded by two probes. The orientation of the E. coli was controlled by adjusting the laser power of probe II. Experimental results were interpreted by theoretical analysis and numerical simulations.